About all

Menopause at 48 years old. Menopause at 48: Understanding Symptoms, Signs, and Treatment Options

When does menopause typically start. What are the most common symptoms of menopause. How long do menopausal symptoms usually last. What treatment options are available for managing menopause symptoms. Is hormone therapy safe for menopausal women. How does menopause impact overall health and longevity. What lifestyle changes can help ease the transition through menopause.

Содержание

The Timing and Significance of Natural Menopause

Natural menopause, defined as the final menstrual period, typically occurs around age 51 for women in Western countries. However, the age of onset can vary widely, with some women experiencing menopause in their 40s and others not until their late 50s. Understanding the timing of menopause is crucial, as it can have significant implications for a woman’s health and longevity.

Research has shown that the age at which a woman experiences natural menopause may be an important marker of overall health and aging. Several studies have found associations between later menopause and various health benefits:

  • Longer overall life expectancy
  • Reduced risk of cardiovascular disease
  • Lower mortality rates from heart disease and stroke
  • Better bone density and reduced risk of osteoporosis
  • Improved cognitive function in later life

However, it’s important to note that later menopause is not universally beneficial. Women who experience menopause at a later age may have an increased risk of certain hormone-sensitive cancers, including breast, endometrial, and ovarian cancers.

Common Symptoms and Signs of Menopause

As women approach menopause, they may experience a variety of symptoms due to hormonal changes. The most frequently reported menopausal symptoms include:

  • Hot flashes and night sweats
  • Irregular periods
  • Mood changes and irritability
  • Vaginal dryness and discomfort
  • Sleep disturbances
  • Weight gain and slowed metabolism
  • Thinning hair and dry skin
  • Loss of breast fullness

Do all women experience the same menopausal symptoms? The short answer is no. The severity and duration of symptoms can vary greatly among individuals. Some women may have minimal discomfort, while others experience significant disruptions to their daily lives.

The Menopausal Transition: Perimenopause to Postmenopause

The journey through menopause is not a sudden event but rather a gradual transition that occurs over several years. This transition period is often divided into three stages:

Perimenopause

Perimenopause typically begins in a woman’s 40s, but can start as early as the mid-30s. During this stage, the ovaries gradually produce less estrogen, leading to fluctuations in hormone levels. Periods may become irregular, and some menopausal symptoms may begin to appear.

Menopause

Menopause is officially diagnosed when a woman has gone 12 consecutive months without a menstrual period. At this point, the ovaries have stopped releasing eggs and producing most of their estrogen.

Postmenopause

The years following menopause are referred to as postmenopause. During this time, menopausal symptoms may ease for many women, but the health risks associated with decreased estrogen levels continue to rise.

Factors Influencing the Timing of Menopause

While the average age of menopause is around 51, various factors can influence when a woman experiences her final menstrual period:

  • Genetics and family history
  • Smoking (associated with earlier menopause)
  • Body mass index (BMI)
  • Ethnicity and race
  • Socioeconomic status
  • Diet and nutrition
  • Reproductive history (e.g., number of pregnancies)
  • Certain medical conditions and treatments

Can lifestyle choices affect the onset of menopause? Research suggests that certain habits, particularly smoking, can lead to earlier menopause. Conversely, maintaining a healthy weight and balanced diet may help delay the onset of menopause.

Health Implications of Early and Late Menopause

The timing of menopause can have significant health implications for women. Early menopause, occurring before age 45, has been associated with:

  • Increased risk of cardiovascular disease
  • Higher risk of osteoporosis and fractures
  • Potential cognitive decline
  • Increased risk of certain cancers

On the other hand, late menopause (after age 55) may offer some health benefits but also comes with risks:

  • Reduced risk of cardiovascular disease and osteoporosis
  • Potential for improved cognitive function
  • Increased risk of breast, ovarian, and endometrial cancers

How does the timing of menopause affect a woman’s overall health trajectory? The age at which a woman experiences menopause can influence her long-term health risks and may guide preventive health strategies.

Managing Menopausal Symptoms: Treatment Options and Lifestyle Changes

While menopause is a natural biological process, the associated symptoms can be disruptive to daily life. Fortunately, there are various treatment options and lifestyle modifications that can help manage these symptoms:

Hormone Therapy (HT)

Hormone therapy, involving estrogen and sometimes progesterone, remains one of the most effective treatments for menopausal symptoms, particularly hot flashes and vaginal dryness. However, HT is not without risks and should be used at the lowest effective dose for the shortest duration necessary.

Non-Hormonal Medications

For women who cannot or choose not to use hormone therapy, several non-hormonal medications can help manage specific symptoms:

  • Low-dose antidepressants for hot flashes
  • Gabapentin for hot flashes and sleep disturbances
  • Ospemifene for vaginal dryness and painful intercourse

Lifestyle Modifications

Simple changes in daily habits can often provide significant relief from menopausal symptoms:

  • Regular exercise
  • Stress reduction techniques (e.g., yoga, meditation)
  • Maintaining a healthy weight
  • Avoiding trigger foods and beverages (e.g., spicy foods, caffeine, alcohol)
  • Dressing in layers to manage hot flashes
  • Improving sleep hygiene

Which lifestyle changes are most effective for managing menopausal symptoms? While individual responses may vary, many women find that a combination of regular exercise, stress management, and dietary adjustments can significantly improve their quality of life during the menopausal transition.

The Role of Diet and Nutrition in Menopause

A healthy diet can play a crucial role in managing menopausal symptoms and promoting overall health during this transitional period. Key dietary considerations include:

  • Calcium and vitamin D for bone health
  • Phytoestrogens (found in soy products, flaxseeds, and certain fruits and vegetables)
  • Omega-3 fatty acids for heart and cognitive health
  • Adequate protein intake to maintain muscle mass
  • Foods rich in antioxidants to support overall health

Can certain foods help alleviate menopausal symptoms? Some studies suggest that foods rich in phytoestrogens may help reduce hot flashes and other menopausal symptoms, although more research is needed to confirm these effects.

The Importance of Regular Health Screenings During and After Menopause

As women transition through menopause, regular health screenings become increasingly important. Key screenings and check-ups include:

  • Mammograms for breast cancer detection
  • Bone density scans to assess osteoporosis risk
  • Lipid profiles to monitor cardiovascular health
  • Pap smears and pelvic exams
  • Thyroid function tests
  • Colonoscopies for colorectal cancer screening

How often should postmenopausal women undergo health screenings? The frequency of screenings may vary based on individual risk factors and health history. It’s essential for women to consult with their healthcare providers to develop a personalized screening schedule.

In conclusion, menopause is a significant life transition that affects women in various ways. Understanding the timing, symptoms, and health implications of menopause can empower women to navigate this change more effectively. By working closely with healthcare providers and adopting healthy lifestyle habits, women can manage menopausal symptoms and promote long-term health and well-being. As research in this field continues to evolve, our understanding of menopause and its impact on women’s health will undoubtedly expand, leading to improved strategies for supporting women through this important life stage.

The Timing of the Age at Which Natural Menopause Occurs

Obstet Gynecol Clin North Am. Author manuscript; available in PMC 2012 Sep 1.

Published in final edited form as:

PMCID: PMC3285482

NIHMSID: NIHMS353085

Department of Public Health Sciences and Division of Epidemiology, School of Medicine, University of California, Davis, One Shields Avenue, Med Sci 1C, Davis, CA 95616 USA

Keywords: Menopause, Smoking, Parity, Race/ethnicity, Socioeconomic status, Age, Genetics, Family history, Diet

See other articles in PMC that cite the published article.

The age at the final menstrual period holds intrinsic clinical and public health interest because the age at which natural menopause occurs may be a marker of aging and health.1–3 Later age at natural menopause has been associated with:

  • longer overall survival and greater life expectancy4 and reduced all-cause mortality5;

  • reduced risk of cardiovascular disease4,6–11 and mortality from cardiovascular12 and ischemic heart disease,13 stroke,14 angina after myocardial infarction,15 and atherosclerosis16;

  • less loss of bone density,17 and a reduced risk of osteoporosis18 and fracture19;

  • but an increased risk of breast,20,21 endometrial, and ovarian4,22–25 cancers.

In addition, women who have undergone bilateral oophorectomy under the age of 45 years have been observed to be at increased risk of mortality from cardiovascular disease, particularly if they were not treated with estrogen.26 However, women who underwent natural menopause before age 45 years had an increased risk of ischemic heart disease that was not attenuated by use of hormone therapy.27 Further, early menopause has been associated with earlier decline in cognitive function.28–30 Because 40 million women in the United States alone and several hundred million worldwide31 experienced the menopausal transition between 1990 and 2010 due to the aging of the baby boomer generation,32 millions of women are undergoing or have recently undergone the menopause transition, and the timing of their final natural menstrual periods could have important clinical and health implications, because one third of women’s lives is spent postmenopause.

Although menopause is a universal phenomenon among women, the timing of the onset and the duration of the menopausal transition and the timing of the final menstrual period are not.33 Most of our knowledge and perceptions of menopause have been based largely on studies of white women, and many have been studies of clinic-based, rather than population-based, samples of women. Thus, until recently, much of the knowledge about the timing of the natural final menstrual period has been affected by the nature of the samples of women studied and a number of other methodologic differences in the studies of this phenomenon, which must be considered in comparing and summarizing their results.

METHODOLOGIC CONCERNS

Most studies of the menopausal transition have been cross-sectional, rather than longitudinal, in design, providing an opportunity for distortion of the true picture of the timing of the final natural menstrual period, particularly for understanding factors that precede and may affect the timing of menopause. Further, definitions of menopause or the final menstrual period have varied from study to study in terms of the number of months of amenorrhea considered to represent in retrospect the final menstrual period. Studies have also varied with regard to which factors have been included in multivariable analyses that control simultaneously for the effects of multiple variables, which also makes the studies not directly comparable.

The analysis of age at natural menopause in a number of studies has been calculated as a simple mean, rather than using the less-biased survival or multivariable time-to-event analytic approaches. These last two approaches include more information and observations for every woman studied, because all women are included but withdrawn or censored when they experience surgical menopause, start using menopausal hormone therapy or oral contraceptives (OC; which generally masks the natural cessation of menses), or are still premenopausal.34 Also, the accuracy of reporting of age at menopause can vary by whether menopause was natural and by duration from the time of the final menstrual period to the time of the interview about menopause, the latter being directly affected by the age group of the study sample. 35 Further, in some studies that have reported age at menopause, it is unclear if the age at the final menstrual period is being reported, the more frequent approach, or if the age at cessation of menses plus 1 year of amenorrhea, the World Health Organization’s definition of menopause.31 is what is reported, a more rare occurrence.36 Most studies do not use a hormonally based definition of menopause.

Recently, more information has been published regarding differences in the timing of menopause experienced by samples of women of different socioeconomic, racial/ethnic, and lifestyle backgrounds, and standardization of instruments and definitions has increased, resulting in a fuller, clearer, and more insightful picture regarding the underlying physiology.

SUMMARY OF UNDERLYING PHYSIOLOGY

Menopause is defined as the cessation of menstruation which reflects cessation of ovulation owing to a loss of ovarian follicles, which in turn results in reduced ovarian production of estradiol, the most biologically active form of estrogen,37,38 as well as increased circulating concentrations of follicle-stimulating hormone (FSH) and decreased concentrations of inhibin, which inhibits the release of FSH. 37 Age at menopause may be more sensitive to varying rates of atresia of ovarian follicles39 than to the absolute number of oocytes depleted,40 but menopause is reached when depletion of follicles reaches approximately 1000 (from a peak of 5 million follicles at mid-gestation and 2 million at birth).41,42 The age at which sufficient depletion of follicles occurs is affected by the number of follicles achieving migration to the gonadal ridge during gestation, their mitotic abilities until mid-gestation, and the rate of follicular atresia.42,43

As circulating estrogen concentrations decline during the menopausal transition, variations in the regularity, timing, and nature of menstrual bleeding may occur.44 As menstrual cycles become increasingly irregular, bleeding may occur after an inadequate luteal phase or without ovulation,44 usually indicated by a short luteal phase, characteristic of women over the age of 40 years. 45,46 Such cycles may be associated with insufficient FSH (or insufficient FSH responsiveness of the follicle) in the follicular phase, in turn resulting in lower luteal phase estrogen and progesterone secretion. Lack of a corpus luteum, resulting in estrogen secretion (even hyperestrogenicity45,47) unopposed by progesterone, may lead to profuse bleeding.

The nature and timing of bleeding may vary both within and between women. What is known about the host, environmental, or lifestyle factors that may affect such variation is summarized herein. Although some factors have been identified that are associated with early age at natural menopause, the relation of many has not been examined, and most have not been examined in relation to duration of the perimenopause.

Factors Related to Timing of Menopause

Results from cross-sectional studies have indicated that endocrine changes characteristic of the onset of the perimenopause begin at around age 45. 48 The median age at menopause among white women from industrialized countries ranges between 50 and 52 years and at onset of the perimenopause is 47.5 years,49–53 with slight evidence of increasing age at menopause over time.53–57 These onsets seem to vary by race and ethnicity58–60 and are affected by demographic and lifestyle factors.50,51,55,57–69 Although some studies have reported no familial relationship, 1 study has reported that age at menopause was positively associated with maternal age at menopause,61 and 1 recent study has shown genetic control of age at menopause in a study of twins.70 However, a number of potentially modifiable factors which may affect estrogen metabolism, including body mass index (BMI), diet (particularly calories and alcohol intake), and passive smoke exposure have not been examined, nor has the time-varying effect of these and of the other factors that have been previously identified been examined in longitudinal analyses of sufficiently large and diverse study populations.

Sociodemographic Differences

International and geographic differences

Several studies have indicated that women living in developing countries (including Latin America, Indonesia, Singapore, Pakistan, Chile, and Peru) experience natural menopause several years earlier than those in developed countries.71–76 Some work has also indicated that women living in urban areas have a later natural menopause than women in rural areas.62 Women living at high altitude in the Himalayas or in the Andes of Peru undergo natural menopause 1 to 1.5 years earlier than those living at lower altitudes or in less rural areas.72,77–79 It is unclear whether these geographic and international differences in the age at natural menopause reflect genetic, socioeconomic, environmental, racial/ethnic, or lifestyle differences and whether and how these affect physiology.

Racial/ethnic differences

Some studies have reported that African American59 and Latina58,60 women have natural menopause about 2 years earlier than white women. However, 1 small study in Nigeria reported the average age at menopause to be 52.8 years,80 over 1 year later than that generally reported for white women in industrialized nations. Mayan women, despite their high parity (see Reproductive History), have been reported to experience natural menopause fairly early, at about age 45.81 In contrast, Asian women tend to have similar age at menopause to Caucasian women,58,82 although Thai women have been reported to have a lower median age at menopause, at age 49.5 years, despite their high parity,83 and Filipino Malay women have been reported to have an earlier average age at natural menopause at 47 to 48 years.84

Differences by socioeconomic status

A number of studies have observed that lower social class, as measured by the woman’s educational attainment or by her own or her husband’s occupation, is associated with an earlier age at natural menopause.51–54,57,58,61,71,85,86 However, results from a British birth cohort indicated that early life socioeconomic status (SES) was more strongly associated than adult status with age at natural menopause,87 although even the relation of early life SES was greatly attenuated when adjusted for childhood cognitive ability and having been breastfed. 88 One study found that education was more strongly associated with age at natural menopause than occupation.52 Most studies that have examined the relation of marital status have found that single women undergo an earlier natural menopause, and this association cannot be explained by nulliparity.52,89,90

Health-Related Influences

Menstrual and reproductive history

The age at which the final natural menstrual period occurs may be a marker for hormonal status or changes earlier in life.91 In the landmark Treloar longitudinal study of largely white, well-educated women, those whose median menstrual cycle length between the ages of 20 and 35 years was fewer than 26 days underwent natural menopause 1.4 years earlier than women with cycle lengths between 26 and 32 days, whereas a later natural menopause (mean = 0.8 year later) was observed in women with cycle lengths of 33 days or longer.92 In addition, 9 or more days of variability in cycle length has been associated with a later age at natural menopause in this and other studies,52,59 although 1 study reported an earlier natural menopause in women with irregular menses. 53

Increasing parity, particularly among women of higher SES, has also been associated with later age at natural menopause,50–52,55,57,58,61,90,91,93–96 consistent with the theory that natural menopause occurs after oocytes have been sufficiently depleted.93 Although some studies have reported no familial relationship, 1 study reported that women’s age at natural menopause was positively associated with their mother’s age at natural menopause,61 and 1 study of twins showed genetic control of age at natural menopause.70 Age at menarche has been fairly consistently observed not to be associated with age at menopause, after adjusting for parity and cycle length,52,53,55,83,89,97,98 as have prior spontaneous abortion, age at first birth, and history of breastfeeding.52,97,98

A number of studies have reported that women who have used OCs have a later age at natural menopause.52,58,61,63,72,98 an observation that is also consistent with the theory that OCs delay depletion of oocytes. However, the finding has not been wholly consistent across studies, because 1 study reported that this delay became nonsignificant after a time-dependent adjustment for when OCs were used,52 and another study reported that OC users had a significantly earlier natural menopause than nonusers, although this association was not consistent across 5-year age groups.50

Body mass and composition

Several studies have examined the relation of body mass to age at menopause, with inconsistent findings. Some studies have reported that both increased BMI (indicated by weight over height squared) and upper body fat distribution (indicated by waist-to-hip ratio) were associated with later age at natural menopause50,57,96,99,100 and increased sex hormone concentrations.100 However, at least as many other studies have reported no significant association of BMI with age at natural menopause.51,52,54,59,101,102 Some studies have found a relationship between lower weight69 or increased upper body fat distribution101 and earlier age at natural menopause, particularly among smokers. One study reported earlier natural menopause in women on weight reduction programs or who had gained more than 26 pounds between the ages of 20 and 45 years.59

Some of these apparently inconsistent findings may be explained by differences in study design (cross-sectional or retrospective vs prospective) or analysis (eg, inadequate or varying control of confounding variables or survival analysis vs. comparison of crude means). In general, the better designed and analyzed studies have shown no relation of body mass or body fat distribution to age at the final natural menstrual period. Although body mass and composition may be related to age at natural menopause, they are also related inversely to physical activity, alcohol consumption, and education, and positively related to infertility and parity.103 Further research is needed in which all of these potentially confounding variables are simultaneously controlled in the statistical analyses of data from large study samples to be able to assess adequately the independent contribution or interactive effect of body mass and composition and these other factors on the age at the natural final menstrual period and duration of menopause transition, using appropriate longitudinal study design and data analysis techniques.

Familial, genetic, and early childhood factors

In recent years, studies of factors related to age at natural menopause have begun to focus on genetic factors that may be related. Results of family and twin studies suggest that familial and genetic factors may play an important role, with estimates of heritability ranging from 30% to 85%.70,104,105 In 1 relatively large cross-sectional study and 1 large longitudinal British birth cohort study, a strong association was found between mothers’ and daughters’ ages at natural menopause,88,106 which have also been found in a few other smaller studies,107–109 but few longitudinal studies have investigated this relationship. One European genome-wide association study of nearly 3000 women identified 6 single nucleotide polymorphisms in 3 loci on chromosomes 13, 19, and 20 associated with age at natural menopause.110 A Dutch study showed that polymorphisms of an estrogen receptor gene were associated with earlier natural and surgical menopause. 111 Results of genome-wide association studies, using samples from thousands of women in the Nurses’ Health Study and the Women’s Genome Health Study, identified 13 single nucleotide polymorphisms on 4 chromosomes that were associated with age at menopause.112 Analyses of candidate genes from 9 biologically plausible pathways, using the same samples from the same women in these 2 studies, indicated that the steroid hormone metabolism and biosynthesis pathways were associated with age at natural menopause and that genes involved in premature ovarian failure were also significantly associated with age at menopause.113 Two single nucleotide polymorphisms of the tumor necrosis factor receptor family have also been shown to be significantly associated with age at natural menopause.114

A number of analyses have been conducted on prospective data collected across the lifespan from a nationally representative birth cohort of nearly 1600 British women born in 1946 and followed to age 53 years, the Medical Research Council National Survey of Health and Development. These analyses have revealed that women who had a low weight at 2 years of age had an earlier natural menopause,115 whereas those who were heaviest at 2 years of age had a later natural menopause.89 Those who were breastfed had a later natural menopause.115 Another cohort study in England also found that low weight at 1 year of age was associated with earlier natural menopause.116 However, an Australian twin study and the English cohort study found no association of birth weight with age at natural menopause.116,117 The British birth cohort and other cohort studies have shown that poorer cognitive ability in childhood was associated with earlier natural menopause,118–120 suggesting that perhaps markers in early life may determine not only age at natural menopause, but may also predict the adverse health outcomes that are associated with early age at menopause. Further, additional findings from the British birth cohort indicate that women whose parents divorced early in their lives had an earlier natural menopause than other women, suggesting that early life stressors may also be related to early menopause. 87,88

Environmental Influences

Active and passive smoke exposure

Perhaps the single most consistently shown environmental effect on age at menopause is that women who smoke stop menstruating 1 to 2 years earlier than comparable nonsmokers.50,51,55,57–59,61,63–68,86,96,121 and have a shorter perimenopause.122 Some studies have shown a dose–response effect on atrophy of ovarian follicles, in that heavy smokers have an earlier natural menopause than light smokers.61,67,69,123,124 Former smokers have only a slightly earlier age at natural menopause than those who never smoked, and increased time since quitting diminishes the difference.123,125 The latter observation of only a slightly earlier natural menopause in former smokers is inconsistent with the presumed toxic effect of smoking on ovarian follicles, resulting in their atrophy and thus earlier menopause, because such an effect should be nonreversible so that former smokers would also experience the earlier natural menopause observed in current smokers. If the dose–response effect is a true effect, the apparent paradox might partly be explained by fewer years of smoking and thus toxic exposure to the ovaries in former smokers than in current smokers of similar age.

The polycyclic aromatic hydrocarbons in cigarette smoke are known to be toxic to ovarian follicles126,127 and thus could result in premature loss of ovarian follicles and early natural menopause among smokers. Because drug metabolism is enhanced in smokers,128 estrogen also may be more rapidly metabolized in the livers of smokers, which could lead to an earlier reduction of estrogen levels.99 Further, smoking has also been observed to have antiestrogenic effects.129 Greater prevalence of hysterectomy among premenopausal smokers than nonsmokers100,123 apparently does not account for smokers having an earlier natural menopause.130 Only 1 study has shown that nonsmoking women whose spouses smoked had an age at natural menopause resembling that of smokers131; thus, very little is known about the effect of passive or secondhand smoke exposure on the age at which the final natural menstrual period is experienced.

Occupational/environmental factors

Although almost nothing is known about the relations of occupational or other environmental factors to age at the final natural menstrual period and duration of the menopausal transition, occupational exposures and stressors (such as shift work, hours worked, hours spent standing, and heavy lifting) have been related to increased risk of adverse pregnancy outcomes132–135 and changes in menstrual cycle length and variability as well as fecundability.136–139 In addition, such environmental exposures as dichlorodiphenyltrichloroethane and polychlorinated biphenyls have been shown to have estrogenic activity and to be associated with an increased risk of breast cancer,140,141 although this association has not been consistently observed.142,143 Thus, the presumed endocrine effects of such exposures make it reasonable to expect that occupational and environmental exposures may be related to endocrine disruption that is reflected in altered age at natural menopause. One study showed a modest effect on age at natural menopause in women in Seveso, Italy, who were exposed to 2,3,7,8-tetrachlorobenzo-p-dioxin, a halogenated compound that may affect ovarian function, during a chemical plant explosion in 1976.144 Another study showed that exposure to 1,1-dichloro-2,2-bis(p-chlorophenyl) ethylene was also associated with earlier natural menopause.145

Physical activity

Physical activity is associated with a number of changes in hormonal parameters [estradiol, progesterone, prolactin, luteinizing hormone (LH), and FSH), both during and after intense physical activity.146–148 The concentrations of these hormones tend to be lower at rest among women who are physically active.146,147,149,150 Also, athletes tend to have a later age at menarche and increased occurrences of anovulation151 and amenorrhea152 and, among those who menstruate, a shortened luteal phase and reduced mean and peak progesterone levels. 104,149 Although physical activity is associated with decreased concentrations of reproductive hormones and frequency of ovulation, few studies have examined the effect of exercise on age at natural menopause, although 1 modestly sized study reported no relationship,59 and 1 large study of Chinese women showed a later age at natural menopause associated with leisure time physical activity during adolescence and adulthood.94

Diet

One early study from Papua, New Guinea, suggested that malnourished women ceased menstruation about 4 years earlier than well-nourished women,153 consistent with other studies showing that women with greater weight62,69 and height89 may have a later age at natural menopause. Findings regarding the relationship of specific dietary patterns to age at menopause have been inconsistent. For example, vegetarians were observed to have an earlier age at natural menopause in 1 study,154 whereas another study in Japan reported that higher green and yellow vegetable intake was significantly associated with later age at natural menopause. 155 Further, a large cross-sectional study of Japanese women found that higher intakes of fat, cholesterol, and coffee were significantly associated with earlier natural menopause after controlling for age, total energy, parity, menarche age, and relative weight.156 A longitudinal study of nearly 5000 German women observed that high carbohydrate consumption and high intake of vegetable, fiber, and cereal products were related to an earlier age at natural menopause, whereas higher intake of total fat, protein, and meat were associated with a later natural menopause.157 The large, prospective Shanghai Women’s Health Study found that higher total intake of calories, fruits, and protein was significantly associated with later age at natural menopause, whereas vegetable, fat, soy, and fiber intakes were not significantly related to age at menopause.94 Inclusion of meat in the diet of vegetarians has been observed to increase the episodic releases of LH and FSH and the length of the menstrual cycle. 158 Thus, meat may modify the interaction of hormones along the hypothalamic-pituitary-ovarian axis. A couple of studies have reported that increased meat or alcohol consumption is significantly associated with later age at menopause, after adjusting for age and smoking.61,121 Dietary fiber (whose intake tends to be inversely related to meat intake) may interrupt enterohepatic circulation of sex hormones, leading to the lower circulating estrogen concentrations among vegetarian women.159 Nonetheless, a low-fat, high-carbohydrate intervention diet to prevent breast cancer in over 2600 women with extensive mammographic density followed for an average 7 years did not influence the timing of natural menopause, except a significantly earlier natural menopause was observed in those with low BMI who were on the intervention diet.160

Premenopausal women administered soy have shown increased plasma estradiol concentrations and follicular phase length, delayed menstruation, and suppressed midcycle surges of LH and FSH. 161 Among postmenopausal women fed soy, FSH and LH did not decrease significantly, nor did sex hormone-binding globulin increase, and little change occurred in endogenous estradiol or body weight, although a small estrogenic effect on vaginal cytology was observed.162 However, the role of dietary fiber, phytoestrogens, fat, protein, and other nutrients in affecting age at menopause and duration of the perimenopause remains to be systematically studied, but has potentially important implications for prevention of chronic disease in midlife and older women.

CONCLUSION

Despite important methodologic differences, the limitations in the study designs used and the populations studied in the accumulating literature regarding factors that affect the age at which the natural final menstrual period is experienced, an interesting and complex picture is emerging. A number of demographic (eg, education, employment, race/ethnicity), menstrual and reproductive (eg, parity and OC use), familial and genetic, and lifestyle (eg, smoking, weight, physical activity and diet) factors seem to be important determinants of the age at which natural menopause occurs. Smoking, lower parity, and lower SES have been found fairly consistently to be associated with earlier menopause, an indicator of reduced longevity. However, the relationships with African American and Latina race/ethnicity, vegetarian diet, and undernutrition, body mass and composition, and physical activity have been inconsistent, possibly owing to varying methodologic approaches and limitations ().

Table 1

Factors related to earlier and later age at natural menopause

Factors Consistently Related to Earlier Age at Natural Menopause (References)Factors Inconsistently Related to Age at Natural Menopause (References)
Low socioeconomic status51–54,57,58,61,71,85–88Race/ethnicity58–60,80–84
Low/parity50–52,55,57,58,61,90,91,93,96Body mass index or body com position50–52,54,57,59,62,69,98–101
Not using oral contraceptives50,52,58,61,63,72,98Physical activity59,94
Active smoking50,51,55,57–59,61,63–69,86,96,121,124–126Dietary (vegetable, meat, fat, fiber) intake61,121,153–157,160

Other relationships remain largely unexplored (eg, passive smoke exposure and occupational and other environmental exposures). Therefore, much remains to be learned about how these factors affect follicular atresia and hormone levels and thus determine the onset and potentially the duration of the perimenopause and the timing of the final menstrual period. Furthermore, increased understanding of the underlying physiologic mechanisms of these influences needs to include potential genetic, metabolic, and racial/ethnic differences in physiologic responses to lifestyle factors and other environmental exposures and the interaction of genetic factors with these lifestyle and environmental factors. Increasing knowledge about these relationships ultimately offers women and their health care providers enhanced understanding and choices, based on greater knowledge, to deal with the individual presentations of menopause.

ACKNOWLEDGMENTS

The Study of Women’s Health Across the Nation (SWAN) has grant support from the National Institutes of Health (NIH), DHHS, through the National Institute on Aging (NIA), the National Institute of Nursing Research (NINR) and the NIH Office of Research on Women’s Health (ORWH) (Grants NR004061; AG012505, AG012535, AG012531, AG012539, AG012546, AG012553, AG012554, AG012495). Dr Gold was supported by AG012554. The content of this article is solely the responsibility of the author and does not necessarily represent the official views of the NIA, NINR, ORWH or the NIH.

REFERENCES

1. Cooper GS, Sandler DP. Age at natural menopause and mortality. Ann Epidemiol. 1998;8:229–35. [PubMed] [Google Scholar]2. Wise AM, Krajnak KM, Kashon ML. Menopause: the aging of multiple pacemakers. Science. 1996;273:67–70. [PubMed] [Google Scholar]3. Snowdon DA, Kane RL, Beeson WL, et al. Is early natural menopause a biologic marker of health and aging? Am J Public Health. 1989;79:709–14. [PMC free article] [PubMed] [Google Scholar]4. Ossewaarde ME, Bots ML, Verbeek ALM, et al. Age at menopause, cause-specific mortality and total life expectancy. Epidemiology. 2005;16:556–62. [PubMed] [Google Scholar]5. Jacobsen BK, Heuch I, Kvale G. Age at natural menopause and all-cause mortality: a 37-year follow-up of 19,731 Norwegian women. Am J Epidemiol. 2003;157:923–9. [PubMed] [Google Scholar]6. De Kleijn MJ, van der Schouw YT, Verbeek AL, et al. Endogenous estrogen exposure and cardiovascular mortality risk in postmenopausal women. Am J Epidemiol. 2002;155:339–45. [PubMed] [Google Scholar]7. Van der Schouw YT, van der Graaf Y, Steyerberg EW, et al. Age at menopause as a risk factor for cardiovascular mortality. Lancet. 1996;347:714–8. [PubMed] [Google Scholar]8. Jacobsen BK, Nilssen S, Heuch I, et al. Does age at natural menopause affect mortality from ischemic heart disease? J Clin Epidemiol. 1997;50:475–9. [PubMed] [Google Scholar]9. Hu FB, Grodstein F, Hennekens CH, et al. Age at natural menopause and risk of cardiovascular disease. Arch Intern Med. 1999;159:1061–6. [PubMed] [Google Scholar]10. Atsma F, Bartelink ML, Grobbec DE, et al. Postmenopausal status and early menopause as independent risk factors for cardiovascular disease: a meta-analysis. Menopause. 2006;13:265–79. [PubMed] [Google Scholar]11. Cui R, Iso H, Toyoshima H, et al. JACC Study Group. Relationships of age at menarche and menopause, and reproductive year with mortality from cardiovascular disease in Japanese postmenopausal women: the JACC study. J Epidemiol. 2006;16:177–84. [PMC free article] [PubMed] [Google Scholar]12. Jansen SC, Temme EH, Schouten EG. Lifetime estrogen exposure versus age at menopause as mortality predictor. Maturitas. 2002;43:105–12. [PubMed] [Google Scholar]13. Jacobsen BK, Knutsen SF, Fraser GE. Age at natural menopause and total mortality and mortality from ischemic heart disease: the Adventist Health Study. J Clin Epidemiol. 1999;52:303–7. [PubMed] [Google Scholar]14. Lisabeth LD, Beiser AS, Brown DL, et al. Age at natural menopause and risk of ischemic stroke The Framingham Heart Study. Stroke. 2009;40:1044–9. [PMC free article] [PubMed] [Google Scholar]16. Joakimsen O, Bonaa KH, Stensland-Bugge E, et al. Population-based study of age at menopause and ultrasound assessed carotid atherosclerosis: the Tromso Study. J Clin Epidemiol. 2000;53:525–30. [PubMed] [Google Scholar]17. Parazzini F, Bidoli E, Franceschi S, et al. Menopause, menstrual and reproductive history, and bone density in northern Italy. J Epidemiol Community Health. 1996;50:519–23. [PMC free article] [PubMed] [Google Scholar]18. Kritz-Silverstein D, Barrett-Connor E. Early menopause, number of reproductive years, and bone mineral density in postmenopausal women. Am J Public Health. 1993;83:983–8. [PMC free article] [PubMed] [Google Scholar]19. Van Der Voort DJ, Van Der Weijer PH, Barentsen R. Early menopause: increased fracture risk at older age. Osteoporos Int. 2003;14:525–30. [PubMed] [Google Scholar]20. Kelsey JL, Gammon MD, John EM. Reproductive factors and breast cancer. Epidemiol Rev. 1993;15:36–47. [PubMed] [Google Scholar]21. Monninkhof EM, van der Schouw YT, Peeters PH. Early age at menopause and breast cancer: are leaner women more protected? A prospective analysis of the Dutch DOM cohort. Breast Cancer Res Treat. 1999;55:285–91. [PubMed] [Google Scholar]22. De Graaff J, Stolte LA. Age at menarche and menopause of uterine cancer patients. Eur J Obstet Gynecol Reprod Biol. 1978;8:187–93. [PubMed] [Google Scholar]23. Franceschi S, La Vecchia C, Booth M, et al. Pooled analysis of 3 European case-control studies of ovarian cancer: II. Age at menarche and at menopause. Int J Cancer. 1991;49:57–61. [PubMed] [Google Scholar]24. Kaaks R, Lukanova A, Kurzer MS. Obesity, endogenous hormones, and endometrial cancer risk: a synthetic review. Cancer Epidemiol Biomarkers Prev. 2002;11:1531–43. [PubMed] [Google Scholar]25. Xu WH, Xiang YB, Ruan ZX, et al. Menstrual and reproductive factors and endometrial cancer risk: results from a population-based case-control study in urban Shanghai. Int J Cancer. 2004;108:613–9. [PubMed] [Google Scholar]26. Rivera CM, Grossardt BR, Rhodes DJ, et al. Increased cardiovascular mortality after early bilateral oophorectomy. Menopause. 2009;16:15–23. [PMC free article] [PubMed] [Google Scholar]27. Lokkegaard E, Jovanovic Z, Heitmann BL, et al. The association between early menopause and risk of ischaemic heart disease: influence of hormone therapy. Maturitas. 2006;53:226–33. [PubMed] [Google Scholar]28. Woods NF, Mitchell ES, Adams C. Memory functioning among midlife women: observations for the Seattle Midlife Women’s health Study. Menopause. 2000;7:257–65. [PubMed] [Google Scholar]29. Halbreich U, Piletz J, Halaris A. Influence of gonadal hormones on neurotransmitters, receptor, cognition and mood. Clin Neuropharmacol. 1992;15(Suppl A):590A–1A. [PubMed] [Google Scholar]30. Kok HS, Kuh D, Cooper R, et al. Cognitive function across the life course and the menopausal transition in a British birth cohort. Menopause. 2006;13:19–27. [PubMed] [Google Scholar]31. World Health Organization . Research on the menopause in the 1990s. World Health Organization; Geneva (Switzerland): 1996. [Google Scholar]32. Skolnick AA. At third meeting, menopause experts make the most of insufficient data. JAMA. 1992;268:2483–5. [PubMed] [Google Scholar]33. Avis NE, Kaufert PA, Lock M, et al. The evolution of menopausal symptoms. Baillieres Clin Endocrinol Metab. 1993;7:17–32. [PubMed] [Google Scholar]34. Cramer DW, Xu H. Predicting age at menopause. Maturitas. 1996;23:319–26. [PubMed] [Google Scholar]35. Hahn RA, Eaker E, Rolka H. Reliability of reported age at menopause. Am J Epidemiol. 1997;146:771–5. [PubMed] [Google Scholar]36. Sowers MF, LaPietra MT. Menopause: its epidemiology and potential association with chronic diseases. Epidemiol Rev. 1995;17:287–302. [PubMed] [Google Scholar]37. Gosden RG. Biology of the menopause: the causes and consequences of ovarian ageing. Academic Press; London: 1985. [Google Scholar]38. Burger HG, Dudley EC, Hopper JL. The endocrinology of the menopausal transition: a cross-sectional study of a population-based sample. J Clin Endocrinol Metab. 1995;80:3537–45. [PubMed] [Google Scholar]39. Soule MR, Bremner WJ. The menopause and climacteric: endocrinologic basis and associated symptomatology. J Am Geriatrics Soc. 1982;30:547. [PubMed] [Google Scholar]40. Thomford PJ, Jelovsek FR, Mattison DR. Effect of oocyte number and rate of atresia on the age of menopause. Repro Toxicol. 1987;1:41–51. [PubMed] [Google Scholar]41. Faddy MJ, Gosden RG, Gougeon A, et al. Accelerated disappearance of ovarian follicles in mid-life: implications for forecasting menopause. Hum Reprod. 1992;7:1342–6. [PubMed] [Google Scholar]43. Aydos SE, Elhan AH, Tukun A. Is telomere length one of the determinants of reproductive life span? Arch Gynecol Obstet. 2005;2727:113–6. [PubMed] [Google Scholar]44. Sherman BM, West JH, Korenman SG. The menopausal transition: analysis of LH, FSH, estradiol and progesterone concentrations during menstrual cycles of older women. J Clin Endocrinol Metab. 1976;42:629–36. [PubMed] [Google Scholar]45. Santoro N, Rosenberg-Brown J, Adel T, et al. Characterization of reproductive hormonal dynamics in the perimenopause. J Clin Endocrinol Metab. 1996;81:1495–1501. [PubMed] [Google Scholar]46. Upton GV. The perimenopause: physiologic correlates and clinical management. J Reprod Med. 1982;27:1–28. [PubMed] [Google Scholar]47. Shideler SE, DeVane GW, Kalra PS, et al. Ovarian pituitary hormone interactions during the menopause. Maturitas. 1989;11:331–9. [PubMed] [Google Scholar]48. Trevoux R, DeBrux J, Castaneir M, et al. Endometrium and plasma hormone profile in the peri-menopause and post-menopause. Maturitas. 1986;8:309–26. [PubMed] [Google Scholar]49. McKinlay SM, Brambilla DJ, Posner JG. The normal menopause transition. Maturitas. 1992;14:103–15. [PubMed] [Google Scholar]50. Greendale G, Hogan P, Kritz-Silverstein D, et al. Age at menopause in women participating in the postmenopausal estrogen/progestins interventions (PEPI) trial: an example of bias introduced by selection criteria. Menopause. 1995;2:27–34. for the PEPI trial investigators. [Google Scholar]51. Luoto R, Laprio J, Uutela A. Age at natural menopause and sociodemographic status in Finland. Am J Epidemiol. 1994;139:64–76. [PubMed] [Google Scholar]52. Stanford JL, Hartge P, Brinton LA, et al. Factors influencing the age at natural menopause. J Chron Dis. 1987;40:995–1002. [PubMed] [Google Scholar]53. Magursky V, Mesko M, Sokolik L. Age at the menopause and onset of the climacteric in women of Martin district, Czechoslovakia. Int J Fertil. 1975;20:17–23. [PubMed] [Google Scholar]54. Gold EB, Sternfeld B, Brown C, et al. The relation of demographic and lifestyle variables to symptoms in a multi-racial/ethnic population of women aged 40-55 years. Am J Epidemiol. 2000;152:463–73. [PubMed] [Google Scholar]55. van Noord PAH, Dubas JS, Dorland M, et al. Age at natural menopause in a population-based screening cohort: the role of menarche, fecundity, and lifestyle factors. Fertil Steril. 1997;68:95–102. [PubMed] [Google Scholar]56. Flint M. Is there a secular trend in age of menopause. Maturitas. 1978;1:133–9. [PubMed] [Google Scholar]57. Rodstrom K, Bengtsson C, Milsom I, et al. Evidence for a secular trend in menopausal age: a population study of women in Gothenburg. Menopause. 2003;10:538–43. [PubMed] [Google Scholar]58. Gold EB, Bromberger J, Crawford S, et al. Factors associated with age at menopause in a multi-ethnic population of women. Am J Epidemiol. 2001;153:865–74. [PubMed] [Google Scholar]59. Bromberger JT, Matthews KA, Kuller LH, et al. Prospective study of the determinants of age at menopause. Am J Epidemiol. 1997;145:124–33. [PubMed] [Google Scholar]60. Alvarado G, Rivera R, Ruiz R, et al. Characteristicas del patron de sangrado menstrual en un grupo de mujeres normales de Durango. Ginecol Obstetr Mex. 1988;56:127–33. [PubMed] [Google Scholar]61. Torgerson DJ, Avenell A, Russell IT, et al. Factors associated with onset of menopause in women aged 45-49. Maturitas. 1994;19:83–92. [PubMed] [Google Scholar]62. MacMahon B, Worcester J. Age at menopause, United States 1960-1962. Vital Health Stat. 1966;19:1–19. [PubMed] [Google Scholar]63. Palmer JR, Rosenberg L, Wise LA, et al. Onset of natural menopause in African American women. Am J Public Health. 2003;93:299–306. [PMC free article] [PubMed] [Google Scholar]64. McKinlay SM, Bifano NL, McKinlay JB. Smoking and age at menopause in women. Ann Intern Med. 1985;103:350–6. [PubMed] [Google Scholar]65. Andersen FS, Transbol I, Christiansen C. Is cigarette smoking a promoter of the menopause. Acta Med Scand. 1982;212:137–9. [PubMed] [Google Scholar]66. Hiatt RA, Fireman BH. Smoking, menopause, and breast cancer. J Natl Cancer Inst. 1986;76:833–8. [PubMed] [Google Scholar]67. Hartz AJ, Kelber S, Borkowf H, et al. The association of smoking with clinical indicators of altered sex steroids—a study of 50,145 women. Pub Health Rep. 1987;102:254–9. [PMC free article] [PubMed] [Google Scholar]68. Brambilla DJ, McKinlay SM. A prospective study of factors affecting age at menopause. J Clin Epidemiol. 1989;42:1031–9. [PubMed] [Google Scholar]69. Willett W, Stampfer MJ, Bain C, et al. Cigarette smoking, relative weight and menopause. Am J Epidemiol. 1983;117:651–8. [PubMed] [Google Scholar]70. Snieder H, MacGregor AJ, Spector ID. Genes control cessation of a woman’s reproductive life: a twin study of hysterectomy and age at menopause. J Clin Endocrinol Met. 1998;83:1875–80. [PubMed] [Google Scholar]71. Castelo-Branco C, Blümel JE, Chedraui P, et al. Age at menopause in Latin America. Menopause. 2006;13:706–12. Erratum in: Menopause 2006;13:850. [PubMed] [Google Scholar]72. Gonzales GF, Villena A. Age at menopause in central Andean Peruvian women. Menopause. 1997;4:32–8. [Google Scholar]73. McCarthy T. The prevalence of symptoms in menopausal women in the Far East: Singapore segment. Maturitas. 1994;19:199–204. [PubMed] [Google Scholar]74. Samil RS, Wishnuwardhani SD. Health of Indonesian women, city-dwellers of perimenopausal age. Maturitas. 1994;19:191–7. [PubMed] [Google Scholar]75. Wasti S, Robinson SC, Akhtar Y, et al. Characteristics of menopause in three groups in Karachi, Pakistan. Maturitas. 1993;16:61–9. [PubMed] [Google Scholar]76. Blumel J, Cubillos M, Brandt A, et al. Some clinical aspects of menopause. Rev Chil Obstet Ginecol. 1988;53:278–82. [PubMed] [Google Scholar]77. Kapoor AK, Kapoor S. The effects of high altitude on age at menarche and menopause. J Biometeor. 1986;30:21–6. [PubMed] [Google Scholar]78. Beall CM. Ages at menopause and menarche in a high altitude Himalayan population. Ann Hum Biol. 1983;10:365–70. [PubMed] [Google Scholar]79. Flint MP. PhD dissertation. City University of New York; 1974. Menarche and menopause in Rajput women. [Google Scholar]80. Otolorin EO, Adeyefa I, Osotimehin BO, et al. Clinical, hormonal and biochemical features of menopausal women in Ibadan, Nigeria. Afr J Med Sci. 1989;18:251–5. [PubMed] [Google Scholar]81. Beyene Y. Cultural significance and physiological manifestations of menopause, a bicultural analysis. Culture Med Psychiatr. 1986;10:47–71. [PubMed] [Google Scholar]82. Boulet M. The menopause and the climacteric in seven Asian countries. In: Sixth International Congress on the Menopause. Parthenon; New Jersey: 1990. [Google Scholar]83. Chompootweep S, Tankeyoon M, Yamarat K, et al. The menopausal age and climacteric complaints in Thai women in Bangkok. Maturitas. 1993;17:63–71. [PubMed] [Google Scholar]84. Ramoso-Jalbuena J. Climacteric Filipino women: a preliminary survey in the Philippines. Maturitas. 19:183–90. [PubMed] [Google Scholar]85. Lawlor DA, Ebrahim S, Smith GD. The association of socio-economic position across the life course and age at menopause: the British Women’s Heart and Health Study. Br J Obstet Gynecol. 2003;110:1078–87. [PubMed] [Google Scholar]86. Santoro N, Brockwell S, Johnston J, et al. Helping midlife women predict the onset of the final menses: SWAN, the Study of Women’s Health Across the Nation. Menopause. 2007;14:415–24. [PubMed] [Google Scholar]87. Hardy R, Kuh D. Social and environmental conditions across the life course and age at menopause in a British birth cohort study. BJOG. 2005;112:346–54. [PubMed] [Google Scholar]88. Mishra G, Hardy R, Kuh D. Are the effects of risk factors for timing of menopause modified by age? Results from a British birth cohort study. Menopause. 2007;14:717–24. [PubMed] [Google Scholar]89. Brand PC, Lehert PH. A new way of looking at environmental variables that may affect the age at menopause. Maturitas. 1978;1:121–32. [PubMed] [Google Scholar]90. McKinlay S, Jefferys M, Thompson B. An investigation of the age at menopause. J Biosoc Sci. 1972;4:161–73. [PubMed] [Google Scholar]91. Whelan EA, Sandler DP, McConnaughey DR, et al. Menstrual and reproductive characteristics and age at natural menopause. Am J Epidemiol. 1990;131:625–32. [PubMed] [Google Scholar]92. Treloar AE, Boynton RE, Behn BG, et al. Variation of the human menstrual cycle through reproductive life. Int J Fertil. 1966;12(Pt 2):77–126. [PubMed] [Google Scholar]93. Soberon J, Calderon JJ, Goldzieher JW. Relation of parity to age at menopause. Am J Obstet Gynecol. 1966;96:96–100. [PubMed] [Google Scholar]94. Dorjgochoo T, Kallianpur A, Gao Y-T, et al. Dietary and lifestyle predictors of age at natural menopause and reproductive span in the Shanghai Women’s Health Study. Menopause. 2008;15:924–33. [PMC free article] [PubMed] [Google Scholar]95. Loh FH, Khin LW, Saw SM, et al. The age of menopause and the menopause transition in a multiracial population: a nation-wide Singapore study. Maturitas. 2005;52:169–80. [PubMed] [Google Scholar]96. Reynolds RF, Obermeyer CM. Age at natural menopause in Spain and the United States: results from the DAMES project. Am J Hum Biol. 2005;17:331–40. [PubMed] [Google Scholar]97. Parazzini F, Negri E, LaVecchia C. Reproductive and general lifestyle determinants of age at menopause. Maturitas. 1992;15:141–9. [PubMed] [Google Scholar]98. van Keep PA, Brand PC, Lehert PH. Factors affecting the age at menopause. J Biosoc Sci Suppl. 1979;6:37–55. [PubMed] [Google Scholar]99. Lindquist O, Bengtsson C. Menopausal age in relation to smoking. Acta Med Scand. 1979;205:73–7. [PubMed] [Google Scholar]100. Daniell HWP. Smoking, obesity, and the menopause. Lancet. 1978;2:373. [PubMed] [Google Scholar]101. den Tonkelaar I, Seidell J. Fat distribution in relation to age, degree of obesity, smoking habits, parity and estrogen use: a cross-sectional study of 11,825 Dutch women participating in the DOM project. Int J Obesity. 1990;14:753–61. [PubMed] [Google Scholar]103. Kaye S, Folsom A, Prineas RJ, et al. The association of body fat distribution with lifestyle and reproductive factors in a population study of postmenopausal women. Int J Obesity. 1990;14:583–91. [PubMed] [Google Scholar]104. Kok HS, van Asselt KM, van der Schouw YT, et al. Genetic studies to identify genes underlying menopause age. Hum Reprod Update. 2005;11:483–93. [PubMed] [Google Scholar]105. Van Asselt KM, Kok HS, Pearson PL, et al. Heritability of menopausal age in mothers and daughters. Fertil Steril. 2004;82:1348–51. [PubMed] [Google Scholar]106. Torgerson DJ, Thomas RE, Reid DM. Mothers and daughters menopausal ages: is there a link? Eur J Obstet Gynecol Reprod Biol. 1997;74:63–6. [PubMed] [Google Scholar]107. Cramer DW, Xu H, Harlow BL. Family history as a predictor of early menopause. Fertil Steril. 1995;64:740–5. [PubMed] [Google Scholar]108. DeBruin JP, Bovenhuis H, VanNoord PA, et al. The role of genetic factors in age at natural menopause. Hum Reprod. 2001;16:2014–8. [PubMed] [Google Scholar]109. Murabito JM, Yang Q, Fox C, et al. Heritability of age at natural menopause in the Framingham Heart Study. J Clin Endocrinol Metab. 2005;90:3427–30. [PubMed] [Google Scholar]110. Stolk L, Zhai G, Van Meurs JB, et al. Loci at chromosomes 13, 19 and 20 influence age at natural menopause. Nat Genet. 2009;41:645–7. [PMC free article] [PubMed] [Google Scholar]111. Weel AE, Uitterlinden AG, Westendorp IC, et al. Estrogen receptor polymorphism predicts the onset of natural and surgical menopause. J Clin Endocrinol Metab. 1999;84:3146–50. [PubMed] [Google Scholar]112. He C, Kraft P, Chen C, et al. Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. Nat Genet. 2009;41:724–8. [PMC free article] [PubMed] [Google Scholar]113. He C, Kraft P, Chasman DI, et al. A large-scale candidate gene association study of age at menarche and age at natural menopause. Hum Genet. 2010;128:515–27. [PMC free article] [PubMed] [Google Scholar]114. Lu Y, Liu P, Recker RR, et al. TNFRSF11A and TNFSF11 are associated with age at menarche and natural menopause in white women. Menopause. 2010;17:1048–54. [PMC free article] [PubMed] [Google Scholar]115. Hardy R, Kuh D. Does early growth influence timing of the menopause? Evidence from a British birth cohort. Hum Reprod. 2002;17:2474–9. [PubMed] [Google Scholar]116. Cresswell JL, Egger P, Fall CH, et al. Is the age of menopause determined in-utero? Early Hum Dev. 1997;49:143–8. [PubMed] [Google Scholar]117. Treloar SA, Sadrzadeh S, Do KA, et al. Birth weight and age at menopause in Australian female twin pairs: exploration of the fetal origin hypothesis. Hum Reprod. 2000;15:55–9. [PubMed] [Google Scholar]118. Kuh D, Butterworth S, Kok H, et al. Childhood cognitive ability and age at menopause: evidence from two cohort studies. Menopause. 2005;12:475–82. [PubMed] [Google Scholar]119. Richards M, Kuh D, Hardy R, et al. Lifetime cognitive function and timing of the natural menopause. Neurology. 1999;53:308–14. [PubMed] [Google Scholar]120. Whalley LJ, Fox HC, Starr JM, et al. Age at natural menopause and cognition. Maturitas. 2004;49:148–56. [PubMed] [Google Scholar]121. Kinney A, Kline J, Levin B. Alcohol, caffeine and smoking in relation to age at menopause. Maturitas. 2006;54:27–38. [PubMed] [Google Scholar]122. McKinlay SM, Brambilla DJ, Posner JG. The normal menopause transition. Maturitas. 1992;14:103–15. [PubMed] [Google Scholar]123. Adena MA, Gallagher HG. Cigarette smoking and the age at menopause. Ann Human Biol. 1982;9:121–30. [PubMed] [Google Scholar]124. Jick H, Porter J, Morrison AS. Relation between smoking and age of natural menopause. Lancet. 1977;1:1354–5. [PubMed] [Google Scholar]125. Midgett AS, Baron JA. Cigarette smoking and the risk of natural menopause. Epidemiol. 1990;1:464–80. [Google Scholar]126. Mattison DR, Thorgierssen SS. Smoking and industrial pollution and their effects on menopause and ovarian cancer. Lancet. 1978;1:187–8. [PubMed] [Google Scholar]127. Essenberg JM, Fagan L, Malerstein AJ. Chronic poisoning of the ovaries and testes of albino rats and mice by nicotine and cigarette smoke. West J Surg Obstet Gynecol. 1951;59:27–32. [PubMed] [Google Scholar]129. Michnovicz J, Hershcopf R, Naganuma H, et al. Increased 2-hydroxylation of estradiol as a possible mechanism for the anti-estrogenic effect of cigarette smoking. N Engl J Med. 1986;315:1305–9. [PubMed] [Google Scholar]130. Krailo MD, Pike MC. Estimation of the distribution of the age at natural menopause from prevalence data. Am J Epidemiol. 1983;117:356–61. [PubMed] [Google Scholar]131. Everson RB, Sandler DP, Wilcox AJ, et al. Effect of passive exposure to smoking on age at natural menopause. Br Med J. 1986;293:792. [PMC free article] [PubMed] [Google Scholar]132. Mamelle N, Laumon B, Lazar P. Prematurity and occupational activity during pregnancy. Am J Epidemiol. 1984;119:309–22. [PubMed] [Google Scholar]134. Beaumont JJ, Swan SH, Hammond SK, et al. Historical cohort investigation of spontaneous abortion in the Semiconductor health Study: methods and analyses of risk in fabrication overall and in fabrication work groups. Am J Ind Med. 1995;28:735–50. [PubMed] [Google Scholar]135. Swan SH, Beaumont JJ, Hammond SK, et al. Historical cohort study of spontaneous abortion among fabrication workers in the Semiconductor Health Study; agent-level analysis. Am J Ind Med. 1995;28:751–70. [PubMed] [Google Scholar]137. Messing K, Saurel-Cubizolles MG, Bourgine M, et al. Menstrual cycle characteristics and work condition of workers in poultry slaughterhouses and canneries. Scand J Work Environ Health. 1992;18:302–9. [PubMed] [Google Scholar]138. Eskenazi B, Gold EB, Samuels SJ, et al. Prospective assessment of fecundability of female semiconductor workers. Am J Ind Med. 1995;28:817–32. [PubMed] [Google Scholar]139. Gold EB, Eskenazi B, Hammond SK, et al. Prospectively assessed menstrual cycle characteristics in female wafer-fabrication and nonfabrication semiconductor employees. Am J Ind Med. 1995;28:799–816. [PubMed] [Google Scholar]140. Falck F, Jr, Ricci A, Jr, Wolff MS, et al. Pesticides and polychlorinated biphenyl residues in human breast lipids and their relation to breast cancer. Arch Environ Health. 1992;47:143–6. [PubMed] [Google Scholar]141. Wolff MS, Toniolo PG, Lee EW, et al. Blood levels of organochlorine residues and risk of breast cancer. J Natl Cancer Inst. 1993;85:648–52. [PubMed] [Google Scholar]142. Krieger N, Wolff MS, Hiatt RA, et al. Breast cancer and serum organochlorines: a prospective study among white, black and Asian women. J Natl Cancer Inst. 1994;86:589–99. [PubMed] [Google Scholar]143. Hunter DJ, Hankinson SE, Laden F, et al. Plasma organochlorine levels and risk of breast cancer. N Engl J Med. 1997;337:1253–8. [PubMed] [Google Scholar]144. Eskenazi B, Warner M, Marks AR, et al. Serum dioxin concentrations and age at menopause. Environ Health Perspect. 2005;113:858–62. [PMC free article] [PubMed] [Google Scholar]145. Cooper GS, Savitz DA, Millikan R, et al. Organochlorine exposure and age at natural menopause. Epidemiol. 2002;13:729–33. [PubMed] [Google Scholar]146. Cummings SR, Kelsey J, Nevitt MC, et al. Epidemiology of osteoporosis and osteoporotic fractures. Epidemiol Rev. 1985;7:178–208. [PubMed] [Google Scholar]147. Bonen A, Ling WH, Belcastro AN, et al. Profiles of selected hormones during menstrual cycles of teenage athletes. J Appl Physiol. 1981;50:545–51. [PubMed] [Google Scholar]148. Jurkowski JE, Joanes NL, Walker C, et al. Ovarian hormonal responses to exercise. J Appl Physiol. 1978;44:109–14. [PubMed] [Google Scholar]149. Loucks AB, Mortola LF, Girtoon L, et al. Alterations in the hypothalamic-pituitary-ovarian and the hypothalamic-pituitary-adrenal axes in athletic women. J Clin Endocrinol Metab. 1989;68:402–11. [PubMed] [Google Scholar]150. Jasienska G, Ziomkiewicz A, Thune I, et al. Habitual physical activity and estradiol levels in women of reproductive age. Eur J Cancer Prev. 2006;15:439–45. [PubMed] [Google Scholar]151. Bernstein L, Ross RK, Lobo RA, et al. The effects of moderate physical activity on menstrual cycle patterns in adolescence: implications for breast cancer prevention. Br J Cancer. 1987;55:681–5. [PMC free article] [PubMed] [Google Scholar]152. Loucks AB, Horvath SM. Athletic amenorrhea: a review. Med Sci Sports Exer. 1985;17:56–72. [PubMed] [Google Scholar]153. Scragg RFR. Menopause and reproductive span in rural Nuigini. Proc Ann Symp Papua New Guinea Med Soc. 1973:126–44. [Google Scholar]154. Baird DD, Trlavsky FA, Anderson JJB. Do vegetarians have earlier menopause? Proc Soc Epidemiol Res. 1988:907–8. [Google Scholar]155. Nagata C, Takatsuka N, Kawakami N, et al. Association of diet with the onset of menopause in Japanese women. Am J Epidemiol. 2000;152:863–7. [PubMed] [Google Scholar]156. Nagata C, Takatsuka N, Inaba S, et al. Association of diet and other lifestyle with onset of menopause in Japanese women. Maturitas. 1998;29:105–13. [PubMed] [Google Scholar]157. Nagel G, Altenburg HP, Nieters A, et al. Reproductive and dietary determinants of the age at menopause in EPIC-Heidelberg. Maturitas. 2005;52:337–47. [PubMed] [Google Scholar]158. Hill PB, Garbaczewski L, Daynes G, et al. Gonadotrophin release and meat consumption in vegetarian women. Am J Clin Nutr. 1986;43:37–41. [PubMed] [Google Scholar]159. Adlercreutz H, Mousavi Y, Loukovaara M, et al. Lignans, isoflavones, sex hormone metabolism and breast cancer. In: Hochberg R, Naftolin F, editors. The new biology of steroid hormones. Raven Press; New York: 1992. pp. 145–54. [Google Scholar]160. Martin LJ, Greenberg CV, Kriukov V, et al. Intervention with a low-fat, high-carbohydrate diet does not influence the timing of menopause. Am J Clin Nutr. 2006;84:920–8. [PubMed] [Google Scholar]161. Cassidy A, Bingham S, Setchell KDR. Biological effects of a diet of soy protein rich in isoflavones on the menstrual cycle of premenopausal women. Am J Clin Nutr. 1994;60:333–40. [PubMed] [Google Scholar]162. Baird DD, Umbach DM, Lansdell L, et al. Dietary intervention study to assess estrogenicity of dietary soy among postmenopausal women. J Clin Endocrinol Metab. 1995;80:1685–90. [PubMed] [Google Scholar]

The Timing of the Age at Which Natural Menopause Occurs

Obstet Gynecol Clin North Am. Author manuscript; available in PMC 2012 Sep 1.

Published in final edited form as:

PMCID: PMC3285482

NIHMSID: NIHMS353085

Department of Public Health Sciences and Division of Epidemiology, School of Medicine, University of California, Davis, One Shields Avenue, Med Sci 1C, Davis, CA 95616 USA

Keywords: Menopause, Smoking, Parity, Race/ethnicity, Socioeconomic status, Age, Genetics, Family history, Diet

See other articles in PMC that cite the published article.

The age at the final menstrual period holds intrinsic clinical and public health interest because the age at which natural menopause occurs may be a marker of aging and health.1–3 Later age at natural menopause has been associated with:

  • longer overall survival and greater life expectancy4 and reduced all-cause mortality5;

  • reduced risk of cardiovascular disease4,6–11 and mortality from cardiovascular12 and ischemic heart disease,13 stroke,14 angina after myocardial infarction,15 and atherosclerosis16;

  • less loss of bone density,17 and a reduced risk of osteoporosis18 and fracture19;

  • but an increased risk of breast,20,21 endometrial, and ovarian4,22–25 cancers.

In addition, women who have undergone bilateral oophorectomy under the age of 45 years have been observed to be at increased risk of mortality from cardiovascular disease, particularly if they were not treated with estrogen.26 However, women who underwent natural menopause before age 45 years had an increased risk of ischemic heart disease that was not attenuated by use of hormone therapy.27 Further, early menopause has been associated with earlier decline in cognitive function.28–30 Because 40 million women in the United States alone and several hundred million worldwide31 experienced the menopausal transition between 1990 and 2010 due to the aging of the baby boomer generation,32 millions of women are undergoing or have recently undergone the menopause transition, and the timing of their final natural menstrual periods could have important clinical and health implications, because one third of women’s lives is spent postmenopause.

Although menopause is a universal phenomenon among women, the timing of the onset and the duration of the menopausal transition and the timing of the final menstrual period are not.33 Most of our knowledge and perceptions of menopause have been based largely on studies of white women, and many have been studies of clinic-based, rather than population-based, samples of women. Thus, until recently, much of the knowledge about the timing of the natural final menstrual period has been affected by the nature of the samples of women studied and a number of other methodologic differences in the studies of this phenomenon, which must be considered in comparing and summarizing their results.

METHODOLOGIC CONCERNS

Most studies of the menopausal transition have been cross-sectional, rather than longitudinal, in design, providing an opportunity for distortion of the true picture of the timing of the final natural menstrual period, particularly for understanding factors that precede and may affect the timing of menopause. Further, definitions of menopause or the final menstrual period have varied from study to study in terms of the number of months of amenorrhea considered to represent in retrospect the final menstrual period. Studies have also varied with regard to which factors have been included in multivariable analyses that control simultaneously for the effects of multiple variables, which also makes the studies not directly comparable.

The analysis of age at natural menopause in a number of studies has been calculated as a simple mean, rather than using the less-biased survival or multivariable time-to-event analytic approaches. These last two approaches include more information and observations for every woman studied, because all women are included but withdrawn or censored when they experience surgical menopause, start using menopausal hormone therapy or oral contraceptives (OC; which generally masks the natural cessation of menses), or are still premenopausal.34 Also, the accuracy of reporting of age at menopause can vary by whether menopause was natural and by duration from the time of the final menstrual period to the time of the interview about menopause, the latter being directly affected by the age group of the study sample. 35 Further, in some studies that have reported age at menopause, it is unclear if the age at the final menstrual period is being reported, the more frequent approach, or if the age at cessation of menses plus 1 year of amenorrhea, the World Health Organization’s definition of menopause.31 is what is reported, a more rare occurrence.36 Most studies do not use a hormonally based definition of menopause.

Recently, more information has been published regarding differences in the timing of menopause experienced by samples of women of different socioeconomic, racial/ethnic, and lifestyle backgrounds, and standardization of instruments and definitions has increased, resulting in a fuller, clearer, and more insightful picture regarding the underlying physiology.

SUMMARY OF UNDERLYING PHYSIOLOGY

Menopause is defined as the cessation of menstruation which reflects cessation of ovulation owing to a loss of ovarian follicles, which in turn results in reduced ovarian production of estradiol, the most biologically active form of estrogen,37,38 as well as increased circulating concentrations of follicle-stimulating hormone (FSH) and decreased concentrations of inhibin, which inhibits the release of FSH. 37 Age at menopause may be more sensitive to varying rates of atresia of ovarian follicles39 than to the absolute number of oocytes depleted,40 but menopause is reached when depletion of follicles reaches approximately 1000 (from a peak of 5 million follicles at mid-gestation and 2 million at birth).41,42 The age at which sufficient depletion of follicles occurs is affected by the number of follicles achieving migration to the gonadal ridge during gestation, their mitotic abilities until mid-gestation, and the rate of follicular atresia.42,43

As circulating estrogen concentrations decline during the menopausal transition, variations in the regularity, timing, and nature of menstrual bleeding may occur.44 As menstrual cycles become increasingly irregular, bleeding may occur after an inadequate luteal phase or without ovulation,44 usually indicated by a short luteal phase, characteristic of women over the age of 40 years. 45,46 Such cycles may be associated with insufficient FSH (or insufficient FSH responsiveness of the follicle) in the follicular phase, in turn resulting in lower luteal phase estrogen and progesterone secretion. Lack of a corpus luteum, resulting in estrogen secretion (even hyperestrogenicity45,47) unopposed by progesterone, may lead to profuse bleeding.

The nature and timing of bleeding may vary both within and between women. What is known about the host, environmental, or lifestyle factors that may affect such variation is summarized herein. Although some factors have been identified that are associated with early age at natural menopause, the relation of many has not been examined, and most have not been examined in relation to duration of the perimenopause.

Factors Related to Timing of Menopause

Results from cross-sectional studies have indicated that endocrine changes characteristic of the onset of the perimenopause begin at around age 45. 48 The median age at menopause among white women from industrialized countries ranges between 50 and 52 years and at onset of the perimenopause is 47.5 years,49–53 with slight evidence of increasing age at menopause over time.53–57 These onsets seem to vary by race and ethnicity58–60 and are affected by demographic and lifestyle factors.50,51,55,57–69 Although some studies have reported no familial relationship, 1 study has reported that age at menopause was positively associated with maternal age at menopause,61 and 1 recent study has shown genetic control of age at menopause in a study of twins.70 However, a number of potentially modifiable factors which may affect estrogen metabolism, including body mass index (BMI), diet (particularly calories and alcohol intake), and passive smoke exposure have not been examined, nor has the time-varying effect of these and of the other factors that have been previously identified been examined in longitudinal analyses of sufficiently large and diverse study populations.

Sociodemographic Differences

International and geographic differences

Several studies have indicated that women living in developing countries (including Latin America, Indonesia, Singapore, Pakistan, Chile, and Peru) experience natural menopause several years earlier than those in developed countries.71–76 Some work has also indicated that women living in urban areas have a later natural menopause than women in rural areas.62 Women living at high altitude in the Himalayas or in the Andes of Peru undergo natural menopause 1 to 1.5 years earlier than those living at lower altitudes or in less rural areas.72,77–79 It is unclear whether these geographic and international differences in the age at natural menopause reflect genetic, socioeconomic, environmental, racial/ethnic, or lifestyle differences and whether and how these affect physiology.

Racial/ethnic differences

Some studies have reported that African American59 and Latina58,60 women have natural menopause about 2 years earlier than white women. However, 1 small study in Nigeria reported the average age at menopause to be 52.8 years,80 over 1 year later than that generally reported for white women in industrialized nations. Mayan women, despite their high parity (see Reproductive History), have been reported to experience natural menopause fairly early, at about age 45.81 In contrast, Asian women tend to have similar age at menopause to Caucasian women,58,82 although Thai women have been reported to have a lower median age at menopause, at age 49.5 years, despite their high parity,83 and Filipino Malay women have been reported to have an earlier average age at natural menopause at 47 to 48 years.84

Differences by socioeconomic status

A number of studies have observed that lower social class, as measured by the woman’s educational attainment or by her own or her husband’s occupation, is associated with an earlier age at natural menopause.51–54,57,58,61,71,85,86 However, results from a British birth cohort indicated that early life socioeconomic status (SES) was more strongly associated than adult status with age at natural menopause,87 although even the relation of early life SES was greatly attenuated when adjusted for childhood cognitive ability and having been breastfed. 88 One study found that education was more strongly associated with age at natural menopause than occupation.52 Most studies that have examined the relation of marital status have found that single women undergo an earlier natural menopause, and this association cannot be explained by nulliparity.52,89,90

Health-Related Influences

Menstrual and reproductive history

The age at which the final natural menstrual period occurs may be a marker for hormonal status or changes earlier in life.91 In the landmark Treloar longitudinal study of largely white, well-educated women, those whose median menstrual cycle length between the ages of 20 and 35 years was fewer than 26 days underwent natural menopause 1.4 years earlier than women with cycle lengths between 26 and 32 days, whereas a later natural menopause (mean = 0.8 year later) was observed in women with cycle lengths of 33 days or longer.92 In addition, 9 or more days of variability in cycle length has been associated with a later age at natural menopause in this and other studies,52,59 although 1 study reported an earlier natural menopause in women with irregular menses. 53

Increasing parity, particularly among women of higher SES, has also been associated with later age at natural menopause,50–52,55,57,58,61,90,91,93–96 consistent with the theory that natural menopause occurs after oocytes have been sufficiently depleted.93 Although some studies have reported no familial relationship, 1 study reported that women’s age at natural menopause was positively associated with their mother’s age at natural menopause,61 and 1 study of twins showed genetic control of age at natural menopause.70 Age at menarche has been fairly consistently observed not to be associated with age at menopause, after adjusting for parity and cycle length,52,53,55,83,89,97,98 as have prior spontaneous abortion, age at first birth, and history of breastfeeding.52,97,98

A number of studies have reported that women who have used OCs have a later age at natural menopause.52,58,61,63,72,98 an observation that is also consistent with the theory that OCs delay depletion of oocytes. However, the finding has not been wholly consistent across studies, because 1 study reported that this delay became nonsignificant after a time-dependent adjustment for when OCs were used,52 and another study reported that OC users had a significantly earlier natural menopause than nonusers, although this association was not consistent across 5-year age groups.50

Body mass and composition

Several studies have examined the relation of body mass to age at menopause, with inconsistent findings. Some studies have reported that both increased BMI (indicated by weight over height squared) and upper body fat distribution (indicated by waist-to-hip ratio) were associated with later age at natural menopause50,57,96,99,100 and increased sex hormone concentrations.100 However, at least as many other studies have reported no significant association of BMI with age at natural menopause.51,52,54,59,101,102 Some studies have found a relationship between lower weight69 or increased upper body fat distribution101 and earlier age at natural menopause, particularly among smokers. One study reported earlier natural menopause in women on weight reduction programs or who had gained more than 26 pounds between the ages of 20 and 45 years.59

Some of these apparently inconsistent findings may be explained by differences in study design (cross-sectional or retrospective vs prospective) or analysis (eg, inadequate or varying control of confounding variables or survival analysis vs. comparison of crude means). In general, the better designed and analyzed studies have shown no relation of body mass or body fat distribution to age at the final natural menstrual period. Although body mass and composition may be related to age at natural menopause, they are also related inversely to physical activity, alcohol consumption, and education, and positively related to infertility and parity.103 Further research is needed in which all of these potentially confounding variables are simultaneously controlled in the statistical analyses of data from large study samples to be able to assess adequately the independent contribution or interactive effect of body mass and composition and these other factors on the age at the natural final menstrual period and duration of menopause transition, using appropriate longitudinal study design and data analysis techniques.

Familial, genetic, and early childhood factors

In recent years, studies of factors related to age at natural menopause have begun to focus on genetic factors that may be related. Results of family and twin studies suggest that familial and genetic factors may play an important role, with estimates of heritability ranging from 30% to 85%.70,104,105 In 1 relatively large cross-sectional study and 1 large longitudinal British birth cohort study, a strong association was found between mothers’ and daughters’ ages at natural menopause,88,106 which have also been found in a few other smaller studies,107–109 but few longitudinal studies have investigated this relationship. One European genome-wide association study of nearly 3000 women identified 6 single nucleotide polymorphisms in 3 loci on chromosomes 13, 19, and 20 associated with age at natural menopause.110 A Dutch study showed that polymorphisms of an estrogen receptor gene were associated with earlier natural and surgical menopause. 111 Results of genome-wide association studies, using samples from thousands of women in the Nurses’ Health Study and the Women’s Genome Health Study, identified 13 single nucleotide polymorphisms on 4 chromosomes that were associated with age at menopause.112 Analyses of candidate genes from 9 biologically plausible pathways, using the same samples from the same women in these 2 studies, indicated that the steroid hormone metabolism and biosynthesis pathways were associated with age at natural menopause and that genes involved in premature ovarian failure were also significantly associated with age at menopause.113 Two single nucleotide polymorphisms of the tumor necrosis factor receptor family have also been shown to be significantly associated with age at natural menopause.114

A number of analyses have been conducted on prospective data collected across the lifespan from a nationally representative birth cohort of nearly 1600 British women born in 1946 and followed to age 53 years, the Medical Research Council National Survey of Health and Development. These analyses have revealed that women who had a low weight at 2 years of age had an earlier natural menopause,115 whereas those who were heaviest at 2 years of age had a later natural menopause.89 Those who were breastfed had a later natural menopause.115 Another cohort study in England also found that low weight at 1 year of age was associated with earlier natural menopause.116 However, an Australian twin study and the English cohort study found no association of birth weight with age at natural menopause.116,117 The British birth cohort and other cohort studies have shown that poorer cognitive ability in childhood was associated with earlier natural menopause,118–120 suggesting that perhaps markers in early life may determine not only age at natural menopause, but may also predict the adverse health outcomes that are associated with early age at menopause. Further, additional findings from the British birth cohort indicate that women whose parents divorced early in their lives had an earlier natural menopause than other women, suggesting that early life stressors may also be related to early menopause. 87,88

Environmental Influences

Active and passive smoke exposure

Perhaps the single most consistently shown environmental effect on age at menopause is that women who smoke stop menstruating 1 to 2 years earlier than comparable nonsmokers.50,51,55,57–59,61,63–68,86,96,121 and have a shorter perimenopause.122 Some studies have shown a dose–response effect on atrophy of ovarian follicles, in that heavy smokers have an earlier natural menopause than light smokers.61,67,69,123,124 Former smokers have only a slightly earlier age at natural menopause than those who never smoked, and increased time since quitting diminishes the difference.123,125 The latter observation of only a slightly earlier natural menopause in former smokers is inconsistent with the presumed toxic effect of smoking on ovarian follicles, resulting in their atrophy and thus earlier menopause, because such an effect should be nonreversible so that former smokers would also experience the earlier natural menopause observed in current smokers. If the dose–response effect is a true effect, the apparent paradox might partly be explained by fewer years of smoking and thus toxic exposure to the ovaries in former smokers than in current smokers of similar age.

The polycyclic aromatic hydrocarbons in cigarette smoke are known to be toxic to ovarian follicles126,127 and thus could result in premature loss of ovarian follicles and early natural menopause among smokers. Because drug metabolism is enhanced in smokers,128 estrogen also may be more rapidly metabolized in the livers of smokers, which could lead to an earlier reduction of estrogen levels.99 Further, smoking has also been observed to have antiestrogenic effects.129 Greater prevalence of hysterectomy among premenopausal smokers than nonsmokers100,123 apparently does not account for smokers having an earlier natural menopause.130 Only 1 study has shown that nonsmoking women whose spouses smoked had an age at natural menopause resembling that of smokers131; thus, very little is known about the effect of passive or secondhand smoke exposure on the age at which the final natural menstrual period is experienced.

Occupational/environmental factors

Although almost nothing is known about the relations of occupational or other environmental factors to age at the final natural menstrual period and duration of the menopausal transition, occupational exposures and stressors (such as shift work, hours worked, hours spent standing, and heavy lifting) have been related to increased risk of adverse pregnancy outcomes132–135 and changes in menstrual cycle length and variability as well as fecundability.136–139 In addition, such environmental exposures as dichlorodiphenyltrichloroethane and polychlorinated biphenyls have been shown to have estrogenic activity and to be associated with an increased risk of breast cancer,140,141 although this association has not been consistently observed.142,143 Thus, the presumed endocrine effects of such exposures make it reasonable to expect that occupational and environmental exposures may be related to endocrine disruption that is reflected in altered age at natural menopause. One study showed a modest effect on age at natural menopause in women in Seveso, Italy, who were exposed to 2,3,7,8-tetrachlorobenzo-p-dioxin, a halogenated compound that may affect ovarian function, during a chemical plant explosion in 1976.144 Another study showed that exposure to 1,1-dichloro-2,2-bis(p-chlorophenyl) ethylene was also associated with earlier natural menopause.145

Physical activity

Physical activity is associated with a number of changes in hormonal parameters [estradiol, progesterone, prolactin, luteinizing hormone (LH), and FSH), both during and after intense physical activity.146–148 The concentrations of these hormones tend to be lower at rest among women who are physically active.146,147,149,150 Also, athletes tend to have a later age at menarche and increased occurrences of anovulation151 and amenorrhea152 and, among those who menstruate, a shortened luteal phase and reduced mean and peak progesterone levels. 104,149 Although physical activity is associated with decreased concentrations of reproductive hormones and frequency of ovulation, few studies have examined the effect of exercise on age at natural menopause, although 1 modestly sized study reported no relationship,59 and 1 large study of Chinese women showed a later age at natural menopause associated with leisure time physical activity during adolescence and adulthood.94

Diet

One early study from Papua, New Guinea, suggested that malnourished women ceased menstruation about 4 years earlier than well-nourished women,153 consistent with other studies showing that women with greater weight62,69 and height89 may have a later age at natural menopause. Findings regarding the relationship of specific dietary patterns to age at menopause have been inconsistent. For example, vegetarians were observed to have an earlier age at natural menopause in 1 study,154 whereas another study in Japan reported that higher green and yellow vegetable intake was significantly associated with later age at natural menopause. 155 Further, a large cross-sectional study of Japanese women found that higher intakes of fat, cholesterol, and coffee were significantly associated with earlier natural menopause after controlling for age, total energy, parity, menarche age, and relative weight.156 A longitudinal study of nearly 5000 German women observed that high carbohydrate consumption and high intake of vegetable, fiber, and cereal products were related to an earlier age at natural menopause, whereas higher intake of total fat, protein, and meat were associated with a later natural menopause.157 The large, prospective Shanghai Women’s Health Study found that higher total intake of calories, fruits, and protein was significantly associated with later age at natural menopause, whereas vegetable, fat, soy, and fiber intakes were not significantly related to age at menopause.94 Inclusion of meat in the diet of vegetarians has been observed to increase the episodic releases of LH and FSH and the length of the menstrual cycle. 158 Thus, meat may modify the interaction of hormones along the hypothalamic-pituitary-ovarian axis. A couple of studies have reported that increased meat or alcohol consumption is significantly associated with later age at menopause, after adjusting for age and smoking.61,121 Dietary fiber (whose intake tends to be inversely related to meat intake) may interrupt enterohepatic circulation of sex hormones, leading to the lower circulating estrogen concentrations among vegetarian women.159 Nonetheless, a low-fat, high-carbohydrate intervention diet to prevent breast cancer in over 2600 women with extensive mammographic density followed for an average 7 years did not influence the timing of natural menopause, except a significantly earlier natural menopause was observed in those with low BMI who were on the intervention diet.160

Premenopausal women administered soy have shown increased plasma estradiol concentrations and follicular phase length, delayed menstruation, and suppressed midcycle surges of LH and FSH. 161 Among postmenopausal women fed soy, FSH and LH did not decrease significantly, nor did sex hormone-binding globulin increase, and little change occurred in endogenous estradiol or body weight, although a small estrogenic effect on vaginal cytology was observed.162 However, the role of dietary fiber, phytoestrogens, fat, protein, and other nutrients in affecting age at menopause and duration of the perimenopause remains to be systematically studied, but has potentially important implications for prevention of chronic disease in midlife and older women.

CONCLUSION

Despite important methodologic differences, the limitations in the study designs used and the populations studied in the accumulating literature regarding factors that affect the age at which the natural final menstrual period is experienced, an interesting and complex picture is emerging. A number of demographic (eg, education, employment, race/ethnicity), menstrual and reproductive (eg, parity and OC use), familial and genetic, and lifestyle (eg, smoking, weight, physical activity and diet) factors seem to be important determinants of the age at which natural menopause occurs. Smoking, lower parity, and lower SES have been found fairly consistently to be associated with earlier menopause, an indicator of reduced longevity. However, the relationships with African American and Latina race/ethnicity, vegetarian diet, and undernutrition, body mass and composition, and physical activity have been inconsistent, possibly owing to varying methodologic approaches and limitations ().

Table 1

Factors related to earlier and later age at natural menopause

Factors Consistently Related to Earlier Age at Natural Menopause (References)Factors Inconsistently Related to Age at Natural Menopause (References)
Low socioeconomic status51–54,57,58,61,71,85–88Race/ethnicity58–60,80–84
Low/parity50–52,55,57,58,61,90,91,93,96Body mass index or body com position50–52,54,57,59,62,69,98–101
Not using oral contraceptives50,52,58,61,63,72,98Physical activity59,94
Active smoking50,51,55,57–59,61,63–69,86,96,121,124–126Dietary (vegetable, meat, fat, fiber) intake61,121,153–157,160

Other relationships remain largely unexplored (eg, passive smoke exposure and occupational and other environmental exposures). Therefore, much remains to be learned about how these factors affect follicular atresia and hormone levels and thus determine the onset and potentially the duration of the perimenopause and the timing of the final menstrual period. Furthermore, increased understanding of the underlying physiologic mechanisms of these influences needs to include potential genetic, metabolic, and racial/ethnic differences in physiologic responses to lifestyle factors and other environmental exposures and the interaction of genetic factors with these lifestyle and environmental factors. Increasing knowledge about these relationships ultimately offers women and their health care providers enhanced understanding and choices, based on greater knowledge, to deal with the individual presentations of menopause.

ACKNOWLEDGMENTS

The Study of Women’s Health Across the Nation (SWAN) has grant support from the National Institutes of Health (NIH), DHHS, through the National Institute on Aging (NIA), the National Institute of Nursing Research (NINR) and the NIH Office of Research on Women’s Health (ORWH) (Grants NR004061; AG012505, AG012535, AG012531, AG012539, AG012546, AG012553, AG012554, AG012495). Dr Gold was supported by AG012554. The content of this article is solely the responsibility of the author and does not necessarily represent the official views of the NIA, NINR, ORWH or the NIH.

REFERENCES

1. Cooper GS, Sandler DP. Age at natural menopause and mortality. Ann Epidemiol. 1998;8:229–35. [PubMed] [Google Scholar]2. Wise AM, Krajnak KM, Kashon ML. Menopause: the aging of multiple pacemakers. Science. 1996;273:67–70. [PubMed] [Google Scholar]3. Snowdon DA, Kane RL, Beeson WL, et al. Is early natural menopause a biologic marker of health and aging? Am J Public Health. 1989;79:709–14. [PMC free article] [PubMed] [Google Scholar]4. Ossewaarde ME, Bots ML, Verbeek ALM, et al. Age at menopause, cause-specific mortality and total life expectancy. Epidemiology. 2005;16:556–62. [PubMed] [Google Scholar]5. Jacobsen BK, Heuch I, Kvale G. Age at natural menopause and all-cause mortality: a 37-year follow-up of 19,731 Norwegian women. Am J Epidemiol. 2003;157:923–9. [PubMed] [Google Scholar]6. De Kleijn MJ, van der Schouw YT, Verbeek AL, et al. Endogenous estrogen exposure and cardiovascular mortality risk in postmenopausal women. Am J Epidemiol. 2002;155:339–45. [PubMed] [Google Scholar]7. Van der Schouw YT, van der Graaf Y, Steyerberg EW, et al. Age at menopause as a risk factor for cardiovascular mortality. Lancet. 1996;347:714–8. [PubMed] [Google Scholar]8. Jacobsen BK, Nilssen S, Heuch I, et al. Does age at natural menopause affect mortality from ischemic heart disease? J Clin Epidemiol. 1997;50:475–9. [PubMed] [Google Scholar]9. Hu FB, Grodstein F, Hennekens CH, et al. Age at natural menopause and risk of cardiovascular disease. Arch Intern Med. 1999;159:1061–6. [PubMed] [Google Scholar]10. Atsma F, Bartelink ML, Grobbec DE, et al. Postmenopausal status and early menopause as independent risk factors for cardiovascular disease: a meta-analysis. Menopause. 2006;13:265–79. [PubMed] [Google Scholar]11. Cui R, Iso H, Toyoshima H, et al. JACC Study Group. Relationships of age at menarche and menopause, and reproductive year with mortality from cardiovascular disease in Japanese postmenopausal women: the JACC study. J Epidemiol. 2006;16:177–84. [PMC free article] [PubMed] [Google Scholar]12. Jansen SC, Temme EH, Schouten EG. Lifetime estrogen exposure versus age at menopause as mortality predictor. Maturitas. 2002;43:105–12. [PubMed] [Google Scholar]13. Jacobsen BK, Knutsen SF, Fraser GE. Age at natural menopause and total mortality and mortality from ischemic heart disease: the Adventist Health Study. J Clin Epidemiol. 1999;52:303–7. [PubMed] [Google Scholar]14. Lisabeth LD, Beiser AS, Brown DL, et al. Age at natural menopause and risk of ischemic stroke The Framingham Heart Study. Stroke. 2009;40:1044–9. [PMC free article] [PubMed] [Google Scholar]16. Joakimsen O, Bonaa KH, Stensland-Bugge E, et al. Population-based study of age at menopause and ultrasound assessed carotid atherosclerosis: the Tromso Study. J Clin Epidemiol. 2000;53:525–30. [PubMed] [Google Scholar]17. Parazzini F, Bidoli E, Franceschi S, et al. Menopause, menstrual and reproductive history, and bone density in northern Italy. J Epidemiol Community Health. 1996;50:519–23. [PMC free article] [PubMed] [Google Scholar]18. Kritz-Silverstein D, Barrett-Connor E. Early menopause, number of reproductive years, and bone mineral density in postmenopausal women. Am J Public Health. 1993;83:983–8. [PMC free article] [PubMed] [Google Scholar]19. Van Der Voort DJ, Van Der Weijer PH, Barentsen R. Early menopause: increased fracture risk at older age. Osteoporos Int. 2003;14:525–30. [PubMed] [Google Scholar]20. Kelsey JL, Gammon MD, John EM. Reproductive factors and breast cancer. Epidemiol Rev. 1993;15:36–47. [PubMed] [Google Scholar]21. Monninkhof EM, van der Schouw YT, Peeters PH. Early age at menopause and breast cancer: are leaner women more protected? A prospective analysis of the Dutch DOM cohort. Breast Cancer Res Treat. 1999;55:285–91. [PubMed] [Google Scholar]22. De Graaff J, Stolte LA. Age at menarche and menopause of uterine cancer patients. Eur J Obstet Gynecol Reprod Biol. 1978;8:187–93. [PubMed] [Google Scholar]23. Franceschi S, La Vecchia C, Booth M, et al. Pooled analysis of 3 European case-control studies of ovarian cancer: II. Age at menarche and at menopause. Int J Cancer. 1991;49:57–61. [PubMed] [Google Scholar]24. Kaaks R, Lukanova A, Kurzer MS. Obesity, endogenous hormones, and endometrial cancer risk: a synthetic review. Cancer Epidemiol Biomarkers Prev. 2002;11:1531–43. [PubMed] [Google Scholar]25. Xu WH, Xiang YB, Ruan ZX, et al. Menstrual and reproductive factors and endometrial cancer risk: results from a population-based case-control study in urban Shanghai. Int J Cancer. 2004;108:613–9. [PubMed] [Google Scholar]26. Rivera CM, Grossardt BR, Rhodes DJ, et al. Increased cardiovascular mortality after early bilateral oophorectomy. Menopause. 2009;16:15–23. [PMC free article] [PubMed] [Google Scholar]27. Lokkegaard E, Jovanovic Z, Heitmann BL, et al. The association between early menopause and risk of ischaemic heart disease: influence of hormone therapy. Maturitas. 2006;53:226–33. [PubMed] [Google Scholar]28. Woods NF, Mitchell ES, Adams C. Memory functioning among midlife women: observations for the Seattle Midlife Women’s health Study. Menopause. 2000;7:257–65. [PubMed] [Google Scholar]29. Halbreich U, Piletz J, Halaris A. Influence of gonadal hormones on neurotransmitters, receptor, cognition and mood. Clin Neuropharmacol. 1992;15(Suppl A):590A–1A. [PubMed] [Google Scholar]30. Kok HS, Kuh D, Cooper R, et al. Cognitive function across the life course and the menopausal transition in a British birth cohort. Menopause. 2006;13:19–27. [PubMed] [Google Scholar]31. World Health Organization . Research on the menopause in the 1990s. World Health Organization; Geneva (Switzerland): 1996. [Google Scholar]32. Skolnick AA. At third meeting, menopause experts make the most of insufficient data. JAMA. 1992;268:2483–5. [PubMed] [Google Scholar]33. Avis NE, Kaufert PA, Lock M, et al. The evolution of menopausal symptoms. Baillieres Clin Endocrinol Metab. 1993;7:17–32. [PubMed] [Google Scholar]34. Cramer DW, Xu H. Predicting age at menopause. Maturitas. 1996;23:319–26. [PubMed] [Google Scholar]35. Hahn RA, Eaker E, Rolka H. Reliability of reported age at menopause. Am J Epidemiol. 1997;146:771–5. [PubMed] [Google Scholar]36. Sowers MF, LaPietra MT. Menopause: its epidemiology and potential association with chronic diseases. Epidemiol Rev. 1995;17:287–302. [PubMed] [Google Scholar]37. Gosden RG. Biology of the menopause: the causes and consequences of ovarian ageing. Academic Press; London: 1985. [Google Scholar]38. Burger HG, Dudley EC, Hopper JL. The endocrinology of the menopausal transition: a cross-sectional study of a population-based sample. J Clin Endocrinol Metab. 1995;80:3537–45. [PubMed] [Google Scholar]39. Soule MR, Bremner WJ. The menopause and climacteric: endocrinologic basis and associated symptomatology. J Am Geriatrics Soc. 1982;30:547. [PubMed] [Google Scholar]40. Thomford PJ, Jelovsek FR, Mattison DR. Effect of oocyte number and rate of atresia on the age of menopause. Repro Toxicol. 1987;1:41–51. [PubMed] [Google Scholar]41. Faddy MJ, Gosden RG, Gougeon A, et al. Accelerated disappearance of ovarian follicles in mid-life: implications for forecasting menopause. Hum Reprod. 1992;7:1342–6. [PubMed] [Google Scholar]43. Aydos SE, Elhan AH, Tukun A. Is telomere length one of the determinants of reproductive life span? Arch Gynecol Obstet. 2005;2727:113–6. [PubMed] [Google Scholar]44. Sherman BM, West JH, Korenman SG. The menopausal transition: analysis of LH, FSH, estradiol and progesterone concentrations during menstrual cycles of older women. J Clin Endocrinol Metab. 1976;42:629–36. [PubMed] [Google Scholar]45. Santoro N, Rosenberg-Brown J, Adel T, et al. Characterization of reproductive hormonal dynamics in the perimenopause. J Clin Endocrinol Metab. 1996;81:1495–1501. [PubMed] [Google Scholar]46. Upton GV. The perimenopause: physiologic correlates and clinical management. J Reprod Med. 1982;27:1–28. [PubMed] [Google Scholar]47. Shideler SE, DeVane GW, Kalra PS, et al. Ovarian pituitary hormone interactions during the menopause. Maturitas. 1989;11:331–9. [PubMed] [Google Scholar]48. Trevoux R, DeBrux J, Castaneir M, et al. Endometrium and plasma hormone profile in the peri-menopause and post-menopause. Maturitas. 1986;8:309–26. [PubMed] [Google Scholar]49. McKinlay SM, Brambilla DJ, Posner JG. The normal menopause transition. Maturitas. 1992;14:103–15. [PubMed] [Google Scholar]50. Greendale G, Hogan P, Kritz-Silverstein D, et al. Age at menopause in women participating in the postmenopausal estrogen/progestins interventions (PEPI) trial: an example of bias introduced by selection criteria. Menopause. 1995;2:27–34. for the PEPI trial investigators. [Google Scholar]51. Luoto R, Laprio J, Uutela A. Age at natural menopause and sociodemographic status in Finland. Am J Epidemiol. 1994;139:64–76. [PubMed] [Google Scholar]52. Stanford JL, Hartge P, Brinton LA, et al. Factors influencing the age at natural menopause. J Chron Dis. 1987;40:995–1002. [PubMed] [Google Scholar]53. Magursky V, Mesko M, Sokolik L. Age at the menopause and onset of the climacteric in women of Martin district, Czechoslovakia. Int J Fertil. 1975;20:17–23. [PubMed] [Google Scholar]54. Gold EB, Sternfeld B, Brown C, et al. The relation of demographic and lifestyle variables to symptoms in a multi-racial/ethnic population of women aged 40-55 years. Am J Epidemiol. 2000;152:463–73. [PubMed] [Google Scholar]55. van Noord PAH, Dubas JS, Dorland M, et al. Age at natural menopause in a population-based screening cohort: the role of menarche, fecundity, and lifestyle factors. Fertil Steril. 1997;68:95–102. [PubMed] [Google Scholar]56. Flint M. Is there a secular trend in age of menopause. Maturitas. 1978;1:133–9. [PubMed] [Google Scholar]57. Rodstrom K, Bengtsson C, Milsom I, et al. Evidence for a secular trend in menopausal age: a population study of women in Gothenburg. Menopause. 2003;10:538–43. [PubMed] [Google Scholar]58. Gold EB, Bromberger J, Crawford S, et al. Factors associated with age at menopause in a multi-ethnic population of women. Am J Epidemiol. 2001;153:865–74. [PubMed] [Google Scholar]59. Bromberger JT, Matthews KA, Kuller LH, et al. Prospective study of the determinants of age at menopause. Am J Epidemiol. 1997;145:124–33. [PubMed] [Google Scholar]60. Alvarado G, Rivera R, Ruiz R, et al. Characteristicas del patron de sangrado menstrual en un grupo de mujeres normales de Durango. Ginecol Obstetr Mex. 1988;56:127–33. [PubMed] [Google Scholar]61. Torgerson DJ, Avenell A, Russell IT, et al. Factors associated with onset of menopause in women aged 45-49. Maturitas. 1994;19:83–92. [PubMed] [Google Scholar]62. MacMahon B, Worcester J. Age at menopause, United States 1960-1962. Vital Health Stat. 1966;19:1–19. [PubMed] [Google Scholar]63. Palmer JR, Rosenberg L, Wise LA, et al. Onset of natural menopause in African American women. Am J Public Health. 2003;93:299–306. [PMC free article] [PubMed] [Google Scholar]64. McKinlay SM, Bifano NL, McKinlay JB. Smoking and age at menopause in women. Ann Intern Med. 1985;103:350–6. [PubMed] [Google Scholar]65. Andersen FS, Transbol I, Christiansen C. Is cigarette smoking a promoter of the menopause. Acta Med Scand. 1982;212:137–9. [PubMed] [Google Scholar]66. Hiatt RA, Fireman BH. Smoking, menopause, and breast cancer. J Natl Cancer Inst. 1986;76:833–8. [PubMed] [Google Scholar]67. Hartz AJ, Kelber S, Borkowf H, et al. The association of smoking with clinical indicators of altered sex steroids—a study of 50,145 women. Pub Health Rep. 1987;102:254–9. [PMC free article] [PubMed] [Google Scholar]68. Brambilla DJ, McKinlay SM. A prospective study of factors affecting age at menopause. J Clin Epidemiol. 1989;42:1031–9. [PubMed] [Google Scholar]69. Willett W, Stampfer MJ, Bain C, et al. Cigarette smoking, relative weight and menopause. Am J Epidemiol. 1983;117:651–8. [PubMed] [Google Scholar]70. Snieder H, MacGregor AJ, Spector ID. Genes control cessation of a woman’s reproductive life: a twin study of hysterectomy and age at menopause. J Clin Endocrinol Met. 1998;83:1875–80. [PubMed] [Google Scholar]71. Castelo-Branco C, Blümel JE, Chedraui P, et al. Age at menopause in Latin America. Menopause. 2006;13:706–12. Erratum in: Menopause 2006;13:850. [PubMed] [Google Scholar]72. Gonzales GF, Villena A. Age at menopause in central Andean Peruvian women. Menopause. 1997;4:32–8. [Google Scholar]73. McCarthy T. The prevalence of symptoms in menopausal women in the Far East: Singapore segment. Maturitas. 1994;19:199–204. [PubMed] [Google Scholar]74. Samil RS, Wishnuwardhani SD. Health of Indonesian women, city-dwellers of perimenopausal age. Maturitas. 1994;19:191–7. [PubMed] [Google Scholar]75. Wasti S, Robinson SC, Akhtar Y, et al. Characteristics of menopause in three groups in Karachi, Pakistan. Maturitas. 1993;16:61–9. [PubMed] [Google Scholar]76. Blumel J, Cubillos M, Brandt A, et al. Some clinical aspects of menopause. Rev Chil Obstet Ginecol. 1988;53:278–82. [PubMed] [Google Scholar]77. Kapoor AK, Kapoor S. The effects of high altitude on age at menarche and menopause. J Biometeor. 1986;30:21–6. [PubMed] [Google Scholar]78. Beall CM. Ages at menopause and menarche in a high altitude Himalayan population. Ann Hum Biol. 1983;10:365–70. [PubMed] [Google Scholar]79. Flint MP. PhD dissertation. City University of New York; 1974. Menarche and menopause in Rajput women. [Google Scholar]80. Otolorin EO, Adeyefa I, Osotimehin BO, et al. Clinical, hormonal and biochemical features of menopausal women in Ibadan, Nigeria. Afr J Med Sci. 1989;18:251–5. [PubMed] [Google Scholar]81. Beyene Y. Cultural significance and physiological manifestations of menopause, a bicultural analysis. Culture Med Psychiatr. 1986;10:47–71. [PubMed] [Google Scholar]82. Boulet M. The menopause and the climacteric in seven Asian countries. In: Sixth International Congress on the Menopause. Parthenon; New Jersey: 1990. [Google Scholar]83. Chompootweep S, Tankeyoon M, Yamarat K, et al. The menopausal age and climacteric complaints in Thai women in Bangkok. Maturitas. 1993;17:63–71. [PubMed] [Google Scholar]84. Ramoso-Jalbuena J. Climacteric Filipino women: a preliminary survey in the Philippines. Maturitas. 19:183–90. [PubMed] [Google Scholar]85. Lawlor DA, Ebrahim S, Smith GD. The association of socio-economic position across the life course and age at menopause: the British Women’s Heart and Health Study. Br J Obstet Gynecol. 2003;110:1078–87. [PubMed] [Google Scholar]86. Santoro N, Brockwell S, Johnston J, et al. Helping midlife women predict the onset of the final menses: SWAN, the Study of Women’s Health Across the Nation. Menopause. 2007;14:415–24. [PubMed] [Google Scholar]87. Hardy R, Kuh D. Social and environmental conditions across the life course and age at menopause in a British birth cohort study. BJOG. 2005;112:346–54. [PubMed] [Google Scholar]88. Mishra G, Hardy R, Kuh D. Are the effects of risk factors for timing of menopause modified by age? Results from a British birth cohort study. Menopause. 2007;14:717–24. [PubMed] [Google Scholar]89. Brand PC, Lehert PH. A new way of looking at environmental variables that may affect the age at menopause. Maturitas. 1978;1:121–32. [PubMed] [Google Scholar]90. McKinlay S, Jefferys M, Thompson B. An investigation of the age at menopause. J Biosoc Sci. 1972;4:161–73. [PubMed] [Google Scholar]91. Whelan EA, Sandler DP, McConnaughey DR, et al. Menstrual and reproductive characteristics and age at natural menopause. Am J Epidemiol. 1990;131:625–32. [PubMed] [Google Scholar]92. Treloar AE, Boynton RE, Behn BG, et al. Variation of the human menstrual cycle through reproductive life. Int J Fertil. 1966;12(Pt 2):77–126. [PubMed] [Google Scholar]93. Soberon J, Calderon JJ, Goldzieher JW. Relation of parity to age at menopause. Am J Obstet Gynecol. 1966;96:96–100. [PubMed] [Google Scholar]94. Dorjgochoo T, Kallianpur A, Gao Y-T, et al. Dietary and lifestyle predictors of age at natural menopause and reproductive span in the Shanghai Women’s Health Study. Menopause. 2008;15:924–33. [PMC free article] [PubMed] [Google Scholar]95. Loh FH, Khin LW, Saw SM, et al. The age of menopause and the menopause transition in a multiracial population: a nation-wide Singapore study. Maturitas. 2005;52:169–80. [PubMed] [Google Scholar]96. Reynolds RF, Obermeyer CM. Age at natural menopause in Spain and the United States: results from the DAMES project. Am J Hum Biol. 2005;17:331–40. [PubMed] [Google Scholar]97. Parazzini F, Negri E, LaVecchia C. Reproductive and general lifestyle determinants of age at menopause. Maturitas. 1992;15:141–9. [PubMed] [Google Scholar]98. van Keep PA, Brand PC, Lehert PH. Factors affecting the age at menopause. J Biosoc Sci Suppl. 1979;6:37–55. [PubMed] [Google Scholar]99. Lindquist O, Bengtsson C. Menopausal age in relation to smoking. Acta Med Scand. 1979;205:73–7. [PubMed] [Google Scholar]100. Daniell HWP. Smoking, obesity, and the menopause. Lancet. 1978;2:373. [PubMed] [Google Scholar]101. den Tonkelaar I, Seidell J. Fat distribution in relation to age, degree of obesity, smoking habits, parity and estrogen use: a cross-sectional study of 11,825 Dutch women participating in the DOM project. Int J Obesity. 1990;14:753–61. [PubMed] [Google Scholar]103. Kaye S, Folsom A, Prineas RJ, et al. The association of body fat distribution with lifestyle and reproductive factors in a population study of postmenopausal women. Int J Obesity. 1990;14:583–91. [PubMed] [Google Scholar]104. Kok HS, van Asselt KM, van der Schouw YT, et al. Genetic studies to identify genes underlying menopause age. Hum Reprod Update. 2005;11:483–93. [PubMed] [Google Scholar]105. Van Asselt KM, Kok HS, Pearson PL, et al. Heritability of menopausal age in mothers and daughters. Fertil Steril. 2004;82:1348–51. [PubMed] [Google Scholar]106. Torgerson DJ, Thomas RE, Reid DM. Mothers and daughters menopausal ages: is there a link? Eur J Obstet Gynecol Reprod Biol. 1997;74:63–6. [PubMed] [Google Scholar]107. Cramer DW, Xu H, Harlow BL. Family history as a predictor of early menopause. Fertil Steril. 1995;64:740–5. [PubMed] [Google Scholar]108. DeBruin JP, Bovenhuis H, VanNoord PA, et al. The role of genetic factors in age at natural menopause. Hum Reprod. 2001;16:2014–8. [PubMed] [Google Scholar]109. Murabito JM, Yang Q, Fox C, et al. Heritability of age at natural menopause in the Framingham Heart Study. J Clin Endocrinol Metab. 2005;90:3427–30. [PubMed] [Google Scholar]110. Stolk L, Zhai G, Van Meurs JB, et al. Loci at chromosomes 13, 19 and 20 influence age at natural menopause. Nat Genet. 2009;41:645–7. [PMC free article] [PubMed] [Google Scholar]111. Weel AE, Uitterlinden AG, Westendorp IC, et al. Estrogen receptor polymorphism predicts the onset of natural and surgical menopause. J Clin Endocrinol Metab. 1999;84:3146–50. [PubMed] [Google Scholar]112. He C, Kraft P, Chen C, et al. Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. Nat Genet. 2009;41:724–8. [PMC free article] [PubMed] [Google Scholar]113. He C, Kraft P, Chasman DI, et al. A large-scale candidate gene association study of age at menarche and age at natural menopause. Hum Genet. 2010;128:515–27. [PMC free article] [PubMed] [Google Scholar]114. Lu Y, Liu P, Recker RR, et al. TNFRSF11A and TNFSF11 are associated with age at menarche and natural menopause in white women. Menopause. 2010;17:1048–54. [PMC free article] [PubMed] [Google Scholar]115. Hardy R, Kuh D. Does early growth influence timing of the menopause? Evidence from a British birth cohort. Hum Reprod. 2002;17:2474–9. [PubMed] [Google Scholar]116. Cresswell JL, Egger P, Fall CH, et al. Is the age of menopause determined in-utero? Early Hum Dev. 1997;49:143–8. [PubMed] [Google Scholar]117. Treloar SA, Sadrzadeh S, Do KA, et al. Birth weight and age at menopause in Australian female twin pairs: exploration of the fetal origin hypothesis. Hum Reprod. 2000;15:55–9. [PubMed] [Google Scholar]118. Kuh D, Butterworth S, Kok H, et al. Childhood cognitive ability and age at menopause: evidence from two cohort studies. Menopause. 2005;12:475–82. [PubMed] [Google Scholar]119. Richards M, Kuh D, Hardy R, et al. Lifetime cognitive function and timing of the natural menopause. Neurology. 1999;53:308–14. [PubMed] [Google Scholar]120. Whalley LJ, Fox HC, Starr JM, et al. Age at natural menopause and cognition. Maturitas. 2004;49:148–56. [PubMed] [Google Scholar]121. Kinney A, Kline J, Levin B. Alcohol, caffeine and smoking in relation to age at menopause. Maturitas. 2006;54:27–38. [PubMed] [Google Scholar]122. McKinlay SM, Brambilla DJ, Posner JG. The normal menopause transition. Maturitas. 1992;14:103–15. [PubMed] [Google Scholar]123. Adena MA, Gallagher HG. Cigarette smoking and the age at menopause. Ann Human Biol. 1982;9:121–30. [PubMed] [Google Scholar]124. Jick H, Porter J, Morrison AS. Relation between smoking and age of natural menopause. Lancet. 1977;1:1354–5. [PubMed] [Google Scholar]125. Midgett AS, Baron JA. Cigarette smoking and the risk of natural menopause. Epidemiol. 1990;1:464–80. [Google Scholar]126. Mattison DR, Thorgierssen SS. Smoking and industrial pollution and their effects on menopause and ovarian cancer. Lancet. 1978;1:187–8. [PubMed] [Google Scholar]127. Essenberg JM, Fagan L, Malerstein AJ. Chronic poisoning of the ovaries and testes of albino rats and mice by nicotine and cigarette smoke. West J Surg Obstet Gynecol. 1951;59:27–32. [PubMed] [Google Scholar]129. Michnovicz J, Hershcopf R, Naganuma H, et al. Increased 2-hydroxylation of estradiol as a possible mechanism for the anti-estrogenic effect of cigarette smoking. N Engl J Med. 1986;315:1305–9. [PubMed] [Google Scholar]130. Krailo MD, Pike MC. Estimation of the distribution of the age at natural menopause from prevalence data. Am J Epidemiol. 1983;117:356–61. [PubMed] [Google Scholar]131. Everson RB, Sandler DP, Wilcox AJ, et al. Effect of passive exposure to smoking on age at natural menopause. Br Med J. 1986;293:792. [PMC free article] [PubMed] [Google Scholar]132. Mamelle N, Laumon B, Lazar P. Prematurity and occupational activity during pregnancy. Am J Epidemiol. 1984;119:309–22. [PubMed] [Google Scholar]134. Beaumont JJ, Swan SH, Hammond SK, et al. Historical cohort investigation of spontaneous abortion in the Semiconductor health Study: methods and analyses of risk in fabrication overall and in fabrication work groups. Am J Ind Med. 1995;28:735–50. [PubMed] [Google Scholar]135. Swan SH, Beaumont JJ, Hammond SK, et al. Historical cohort study of spontaneous abortion among fabrication workers in the Semiconductor Health Study; agent-level analysis. Am J Ind Med. 1995;28:751–70. [PubMed] [Google Scholar]137. Messing K, Saurel-Cubizolles MG, Bourgine M, et al. Menstrual cycle characteristics and work condition of workers in poultry slaughterhouses and canneries. Scand J Work Environ Health. 1992;18:302–9. [PubMed] [Google Scholar]138. Eskenazi B, Gold EB, Samuels SJ, et al. Prospective assessment of fecundability of female semiconductor workers. Am J Ind Med. 1995;28:817–32. [PubMed] [Google Scholar]139. Gold EB, Eskenazi B, Hammond SK, et al. Prospectively assessed menstrual cycle characteristics in female wafer-fabrication and nonfabrication semiconductor employees. Am J Ind Med. 1995;28:799–816. [PubMed] [Google Scholar]140. Falck F, Jr, Ricci A, Jr, Wolff MS, et al. Pesticides and polychlorinated biphenyl residues in human breast lipids and their relation to breast cancer. Arch Environ Health. 1992;47:143–6. [PubMed] [Google Scholar]141. Wolff MS, Toniolo PG, Lee EW, et al. Blood levels of organochlorine residues and risk of breast cancer. J Natl Cancer Inst. 1993;85:648–52. [PubMed] [Google Scholar]142. Krieger N, Wolff MS, Hiatt RA, et al. Breast cancer and serum organochlorines: a prospective study among white, black and Asian women. J Natl Cancer Inst. 1994;86:589–99. [PubMed] [Google Scholar]143. Hunter DJ, Hankinson SE, Laden F, et al. Plasma organochlorine levels and risk of breast cancer. N Engl J Med. 1997;337:1253–8. [PubMed] [Google Scholar]144. Eskenazi B, Warner M, Marks AR, et al. Serum dioxin concentrations and age at menopause. Environ Health Perspect. 2005;113:858–62. [PMC free article] [PubMed] [Google Scholar]145. Cooper GS, Savitz DA, Millikan R, et al. Organochlorine exposure and age at natural menopause. Epidemiol. 2002;13:729–33. [PubMed] [Google Scholar]146. Cummings SR, Kelsey J, Nevitt MC, et al. Epidemiology of osteoporosis and osteoporotic fractures. Epidemiol Rev. 1985;7:178–208. [PubMed] [Google Scholar]147. Bonen A, Ling WH, Belcastro AN, et al. Profiles of selected hormones during menstrual cycles of teenage athletes. J Appl Physiol. 1981;50:545–51. [PubMed] [Google Scholar]148. Jurkowski JE, Joanes NL, Walker C, et al. Ovarian hormonal responses to exercise. J Appl Physiol. 1978;44:109–14. [PubMed] [Google Scholar]149. Loucks AB, Mortola LF, Girtoon L, et al. Alterations in the hypothalamic-pituitary-ovarian and the hypothalamic-pituitary-adrenal axes in athletic women. J Clin Endocrinol Metab. 1989;68:402–11. [PubMed] [Google Scholar]150. Jasienska G, Ziomkiewicz A, Thune I, et al. Habitual physical activity and estradiol levels in women of reproductive age. Eur J Cancer Prev. 2006;15:439–45. [PubMed] [Google Scholar]151. Bernstein L, Ross RK, Lobo RA, et al. The effects of moderate physical activity on menstrual cycle patterns in adolescence: implications for breast cancer prevention. Br J Cancer. 1987;55:681–5. [PMC free article] [PubMed] [Google Scholar]152. Loucks AB, Horvath SM. Athletic amenorrhea: a review. Med Sci Sports Exer. 1985;17:56–72. [PubMed] [Google Scholar]153. Scragg RFR. Menopause and reproductive span in rural Nuigini. Proc Ann Symp Papua New Guinea Med Soc. 1973:126–44. [Google Scholar]154. Baird DD, Trlavsky FA, Anderson JJB. Do vegetarians have earlier menopause? Proc Soc Epidemiol Res. 1988:907–8. [Google Scholar]155. Nagata C, Takatsuka N, Kawakami N, et al. Association of diet with the onset of menopause in Japanese women. Am J Epidemiol. 2000;152:863–7. [PubMed] [Google Scholar]156. Nagata C, Takatsuka N, Inaba S, et al. Association of diet and other lifestyle with onset of menopause in Japanese women. Maturitas. 1998;29:105–13. [PubMed] [Google Scholar]157. Nagel G, Altenburg HP, Nieters A, et al. Reproductive and dietary determinants of the age at menopause in EPIC-Heidelberg. Maturitas. 2005;52:337–47. [PubMed] [Google Scholar]158. Hill PB, Garbaczewski L, Daynes G, et al. Gonadotrophin release and meat consumption in vegetarian women. Am J Clin Nutr. 1986;43:37–41. [PubMed] [Google Scholar]159. Adlercreutz H, Mousavi Y, Loukovaara M, et al. Lignans, isoflavones, sex hormone metabolism and breast cancer. In: Hochberg R, Naftolin F, editors. The new biology of steroid hormones. Raven Press; New York: 1992. pp. 145–54. [Google Scholar]160. Martin LJ, Greenberg CV, Kriukov V, et al. Intervention with a low-fat, high-carbohydrate diet does not influence the timing of menopause. Am J Clin Nutr. 2006;84:920–8. [PubMed] [Google Scholar]161. Cassidy A, Bingham S, Setchell KDR. Biological effects of a diet of soy protein rich in isoflavones on the menstrual cycle of premenopausal women. Am J Clin Nutr. 1994;60:333–40. [PubMed] [Google Scholar]162. Baird DD, Umbach DM, Lansdell L, et al. Dietary intervention study to assess estrogenicity of dietary soy among postmenopausal women. J Clin Endocrinol Metab. 1995;80:1685–90. [PubMed] [Google Scholar]

The Timing of the Age at Which Natural Menopause Occurs

Obstet Gynecol Clin North Am. Author manuscript; available in PMC 2012 Sep 1.

Published in final edited form as:

PMCID: PMC3285482

NIHMSID: NIHMS353085

Department of Public Health Sciences and Division of Epidemiology, School of Medicine, University of California, Davis, One Shields Avenue, Med Sci 1C, Davis, CA 95616 USA

Keywords: Menopause, Smoking, Parity, Race/ethnicity, Socioeconomic status, Age, Genetics, Family history, Diet

See other articles in PMC that cite the published article.

The age at the final menstrual period holds intrinsic clinical and public health interest because the age at which natural menopause occurs may be a marker of aging and health.1–3 Later age at natural menopause has been associated with:

  • longer overall survival and greater life expectancy4 and reduced all-cause mortality5;

  • reduced risk of cardiovascular disease4,6–11 and mortality from cardiovascular12 and ischemic heart disease,13 stroke,14 angina after myocardial infarction,15 and atherosclerosis16;

  • less loss of bone density,17 and a reduced risk of osteoporosis18 and fracture19;

  • but an increased risk of breast,20,21 endometrial, and ovarian4,22–25 cancers.

In addition, women who have undergone bilateral oophorectomy under the age of 45 years have been observed to be at increased risk of mortality from cardiovascular disease, particularly if they were not treated with estrogen.26 However, women who underwent natural menopause before age 45 years had an increased risk of ischemic heart disease that was not attenuated by use of hormone therapy.27 Further, early menopause has been associated with earlier decline in cognitive function.28–30 Because 40 million women in the United States alone and several hundred million worldwide31 experienced the menopausal transition between 1990 and 2010 due to the aging of the baby boomer generation,32 millions of women are undergoing or have recently undergone the menopause transition, and the timing of their final natural menstrual periods could have important clinical and health implications, because one third of women’s lives is spent postmenopause.

Although menopause is a universal phenomenon among women, the timing of the onset and the duration of the menopausal transition and the timing of the final menstrual period are not.33 Most of our knowledge and perceptions of menopause have been based largely on studies of white women, and many have been studies of clinic-based, rather than population-based, samples of women. Thus, until recently, much of the knowledge about the timing of the natural final menstrual period has been affected by the nature of the samples of women studied and a number of other methodologic differences in the studies of this phenomenon, which must be considered in comparing and summarizing their results.

METHODOLOGIC CONCERNS

Most studies of the menopausal transition have been cross-sectional, rather than longitudinal, in design, providing an opportunity for distortion of the true picture of the timing of the final natural menstrual period, particularly for understanding factors that precede and may affect the timing of menopause. Further, definitions of menopause or the final menstrual period have varied from study to study in terms of the number of months of amenorrhea considered to represent in retrospect the final menstrual period. Studies have also varied with regard to which factors have been included in multivariable analyses that control simultaneously for the effects of multiple variables, which also makes the studies not directly comparable.

The analysis of age at natural menopause in a number of studies has been calculated as a simple mean, rather than using the less-biased survival or multivariable time-to-event analytic approaches. These last two approaches include more information and observations for every woman studied, because all women are included but withdrawn or censored when they experience surgical menopause, start using menopausal hormone therapy or oral contraceptives (OC; which generally masks the natural cessation of menses), or are still premenopausal.34 Also, the accuracy of reporting of age at menopause can vary by whether menopause was natural and by duration from the time of the final menstrual period to the time of the interview about menopause, the latter being directly affected by the age group of the study sample.35 Further, in some studies that have reported age at menopause, it is unclear if the age at the final menstrual period is being reported, the more frequent approach, or if the age at cessation of menses plus 1 year of amenorrhea, the World Health Organization’s definition of menopause.31 is what is reported, a more rare occurrence.36 Most studies do not use a hormonally based definition of menopause.

Recently, more information has been published regarding differences in the timing of menopause experienced by samples of women of different socioeconomic, racial/ethnic, and lifestyle backgrounds, and standardization of instruments and definitions has increased, resulting in a fuller, clearer, and more insightful picture regarding the underlying physiology.

SUMMARY OF UNDERLYING PHYSIOLOGY

Menopause is defined as the cessation of menstruation which reflects cessation of ovulation owing to a loss of ovarian follicles, which in turn results in reduced ovarian production of estradiol, the most biologically active form of estrogen,37,38 as well as increased circulating concentrations of follicle-stimulating hormone (FSH) and decreased concentrations of inhibin, which inhibits the release of FSH.37 Age at menopause may be more sensitive to varying rates of atresia of ovarian follicles39 than to the absolute number of oocytes depleted,40 but menopause is reached when depletion of follicles reaches approximately 1000 (from a peak of 5 million follicles at mid-gestation and 2 million at birth).41,42 The age at which sufficient depletion of follicles occurs is affected by the number of follicles achieving migration to the gonadal ridge during gestation, their mitotic abilities until mid-gestation, and the rate of follicular atresia.42,43

As circulating estrogen concentrations decline during the menopausal transition, variations in the regularity, timing, and nature of menstrual bleeding may occur.44 As menstrual cycles become increasingly irregular, bleeding may occur after an inadequate luteal phase or without ovulation,44 usually indicated by a short luteal phase, characteristic of women over the age of 40 years.45,46 Such cycles may be associated with insufficient FSH (or insufficient FSH responsiveness of the follicle) in the follicular phase, in turn resulting in lower luteal phase estrogen and progesterone secretion. Lack of a corpus luteum, resulting in estrogen secretion (even hyperestrogenicity45,47) unopposed by progesterone, may lead to profuse bleeding.

The nature and timing of bleeding may vary both within and between women. What is known about the host, environmental, or lifestyle factors that may affect such variation is summarized herein. Although some factors have been identified that are associated with early age at natural menopause, the relation of many has not been examined, and most have not been examined in relation to duration of the perimenopause.

Factors Related to Timing of Menopause

Results from cross-sectional studies have indicated that endocrine changes characteristic of the onset of the perimenopause begin at around age 45.48 The median age at menopause among white women from industrialized countries ranges between 50 and 52 years and at onset of the perimenopause is 47.5 years,49–53 with slight evidence of increasing age at menopause over time.53–57 These onsets seem to vary by race and ethnicity58–60 and are affected by demographic and lifestyle factors.50,51,55,57–69 Although some studies have reported no familial relationship, 1 study has reported that age at menopause was positively associated with maternal age at menopause,61 and 1 recent study has shown genetic control of age at menopause in a study of twins.70 However, a number of potentially modifiable factors which may affect estrogen metabolism, including body mass index (BMI), diet (particularly calories and alcohol intake), and passive smoke exposure have not been examined, nor has the time-varying effect of these and of the other factors that have been previously identified been examined in longitudinal analyses of sufficiently large and diverse study populations.

Sociodemographic Differences

International and geographic differences

Several studies have indicated that women living in developing countries (including Latin America, Indonesia, Singapore, Pakistan, Chile, and Peru) experience natural menopause several years earlier than those in developed countries.71–76 Some work has also indicated that women living in urban areas have a later natural menopause than women in rural areas.62 Women living at high altitude in the Himalayas or in the Andes of Peru undergo natural menopause 1 to 1.5 years earlier than those living at lower altitudes or in less rural areas.72,77–79 It is unclear whether these geographic and international differences in the age at natural menopause reflect genetic, socioeconomic, environmental, racial/ethnic, or lifestyle differences and whether and how these affect physiology.

Racial/ethnic differences

Some studies have reported that African American59 and Latina58,60 women have natural menopause about 2 years earlier than white women. However, 1 small study in Nigeria reported the average age at menopause to be 52.8 years,80 over 1 year later than that generally reported for white women in industrialized nations. Mayan women, despite their high parity (see Reproductive History), have been reported to experience natural menopause fairly early, at about age 45.81 In contrast, Asian women tend to have similar age at menopause to Caucasian women,58,82 although Thai women have been reported to have a lower median age at menopause, at age 49.5 years, despite their high parity,83 and Filipino Malay women have been reported to have an earlier average age at natural menopause at 47 to 48 years.84

Differences by socioeconomic status

A number of studies have observed that lower social class, as measured by the woman’s educational attainment or by her own or her husband’s occupation, is associated with an earlier age at natural menopause.51–54,57,58,61,71,85,86 However, results from a British birth cohort indicated that early life socioeconomic status (SES) was more strongly associated than adult status with age at natural menopause,87 although even the relation of early life SES was greatly attenuated when adjusted for childhood cognitive ability and having been breastfed.88 One study found that education was more strongly associated with age at natural menopause than occupation.52 Most studies that have examined the relation of marital status have found that single women undergo an earlier natural menopause, and this association cannot be explained by nulliparity.52,89,90

Health-Related Influences

Menstrual and reproductive history

The age at which the final natural menstrual period occurs may be a marker for hormonal status or changes earlier in life.91 In the landmark Treloar longitudinal study of largely white, well-educated women, those whose median menstrual cycle length between the ages of 20 and 35 years was fewer than 26 days underwent natural menopause 1.4 years earlier than women with cycle lengths between 26 and 32 days, whereas a later natural menopause (mean = 0.8 year later) was observed in women with cycle lengths of 33 days or longer.92 In addition, 9 or more days of variability in cycle length has been associated with a later age at natural menopause in this and other studies,52,59 although 1 study reported an earlier natural menopause in women with irregular menses.53

Increasing parity, particularly among women of higher SES, has also been associated with later age at natural menopause,50–52,55,57,58,61,90,91,93–96 consistent with the theory that natural menopause occurs after oocytes have been sufficiently depleted.93 Although some studies have reported no familial relationship, 1 study reported that women’s age at natural menopause was positively associated with their mother’s age at natural menopause,61 and 1 study of twins showed genetic control of age at natural menopause.70 Age at menarche has been fairly consistently observed not to be associated with age at menopause, after adjusting for parity and cycle length,52,53,55,83,89,97,98 as have prior spontaneous abortion, age at first birth, and history of breastfeeding.52,97,98

A number of studies have reported that women who have used OCs have a later age at natural menopause.52,58,61,63,72,98 an observation that is also consistent with the theory that OCs delay depletion of oocytes. However, the finding has not been wholly consistent across studies, because 1 study reported that this delay became nonsignificant after a time-dependent adjustment for when OCs were used,52 and another study reported that OC users had a significantly earlier natural menopause than nonusers, although this association was not consistent across 5-year age groups.50

Body mass and composition

Several studies have examined the relation of body mass to age at menopause, with inconsistent findings. Some studies have reported that both increased BMI (indicated by weight over height squared) and upper body fat distribution (indicated by waist-to-hip ratio) were associated with later age at natural menopause50,57,96,99,100 and increased sex hormone concentrations.100 However, at least as many other studies have reported no significant association of BMI with age at natural menopause.51,52,54,59,101,102 Some studies have found a relationship between lower weight69 or increased upper body fat distribution101 and earlier age at natural menopause, particularly among smokers. One study reported earlier natural menopause in women on weight reduction programs or who had gained more than 26 pounds between the ages of 20 and 45 years.59

Some of these apparently inconsistent findings may be explained by differences in study design (cross-sectional or retrospective vs prospective) or analysis (eg, inadequate or varying control of confounding variables or survival analysis vs. comparison of crude means). In general, the better designed and analyzed studies have shown no relation of body mass or body fat distribution to age at the final natural menstrual period. Although body mass and composition may be related to age at natural menopause, they are also related inversely to physical activity, alcohol consumption, and education, and positively related to infertility and parity.103 Further research is needed in which all of these potentially confounding variables are simultaneously controlled in the statistical analyses of data from large study samples to be able to assess adequately the independent contribution or interactive effect of body mass and composition and these other factors on the age at the natural final menstrual period and duration of menopause transition, using appropriate longitudinal study design and data analysis techniques.

Familial, genetic, and early childhood factors

In recent years, studies of factors related to age at natural menopause have begun to focus on genetic factors that may be related. Results of family and twin studies suggest that familial and genetic factors may play an important role, with estimates of heritability ranging from 30% to 85%.70,104,105 In 1 relatively large cross-sectional study and 1 large longitudinal British birth cohort study, a strong association was found between mothers’ and daughters’ ages at natural menopause,88,106 which have also been found in a few other smaller studies,107–109 but few longitudinal studies have investigated this relationship. One European genome-wide association study of nearly 3000 women identified 6 single nucleotide polymorphisms in 3 loci on chromosomes 13, 19, and 20 associated with age at natural menopause.110 A Dutch study showed that polymorphisms of an estrogen receptor gene were associated with earlier natural and surgical menopause.111 Results of genome-wide association studies, using samples from thousands of women in the Nurses’ Health Study and the Women’s Genome Health Study, identified 13 single nucleotide polymorphisms on 4 chromosomes that were associated with age at menopause.112 Analyses of candidate genes from 9 biologically plausible pathways, using the same samples from the same women in these 2 studies, indicated that the steroid hormone metabolism and biosynthesis pathways were associated with age at natural menopause and that genes involved in premature ovarian failure were also significantly associated with age at menopause.113 Two single nucleotide polymorphisms of the tumor necrosis factor receptor family have also been shown to be significantly associated with age at natural menopause.114

A number of analyses have been conducted on prospective data collected across the lifespan from a nationally representative birth cohort of nearly 1600 British women born in 1946 and followed to age 53 years, the Medical Research Council National Survey of Health and Development. These analyses have revealed that women who had a low weight at 2 years of age had an earlier natural menopause,115 whereas those who were heaviest at 2 years of age had a later natural menopause.89 Those who were breastfed had a later natural menopause.115 Another cohort study in England also found that low weight at 1 year of age was associated with earlier natural menopause.116 However, an Australian twin study and the English cohort study found no association of birth weight with age at natural menopause.116,117 The British birth cohort and other cohort studies have shown that poorer cognitive ability in childhood was associated with earlier natural menopause,118–120 suggesting that perhaps markers in early life may determine not only age at natural menopause, but may also predict the adverse health outcomes that are associated with early age at menopause. Further, additional findings from the British birth cohort indicate that women whose parents divorced early in their lives had an earlier natural menopause than other women, suggesting that early life stressors may also be related to early menopause.87,88

Environmental Influences

Active and passive smoke exposure

Perhaps the single most consistently shown environmental effect on age at menopause is that women who smoke stop menstruating 1 to 2 years earlier than comparable nonsmokers.50,51,55,57–59,61,63–68,86,96,121 and have a shorter perimenopause.122 Some studies have shown a dose–response effect on atrophy of ovarian follicles, in that heavy smokers have an earlier natural menopause than light smokers.61,67,69,123,124 Former smokers have only a slightly earlier age at natural menopause than those who never smoked, and increased time since quitting diminishes the difference.123,125 The latter observation of only a slightly earlier natural menopause in former smokers is inconsistent with the presumed toxic effect of smoking on ovarian follicles, resulting in their atrophy and thus earlier menopause, because such an effect should be nonreversible so that former smokers would also experience the earlier natural menopause observed in current smokers. If the dose–response effect is a true effect, the apparent paradox might partly be explained by fewer years of smoking and thus toxic exposure to the ovaries in former smokers than in current smokers of similar age.

The polycyclic aromatic hydrocarbons in cigarette smoke are known to be toxic to ovarian follicles126,127 and thus could result in premature loss of ovarian follicles and early natural menopause among smokers. Because drug metabolism is enhanced in smokers,128 estrogen also may be more rapidly metabolized in the livers of smokers, which could lead to an earlier reduction of estrogen levels.99 Further, smoking has also been observed to have antiestrogenic effects.129 Greater prevalence of hysterectomy among premenopausal smokers than nonsmokers100,123 apparently does not account for smokers having an earlier natural menopause.130 Only 1 study has shown that nonsmoking women whose spouses smoked had an age at natural menopause resembling that of smokers131; thus, very little is known about the effect of passive or secondhand smoke exposure on the age at which the final natural menstrual period is experienced.

Occupational/environmental factors

Although almost nothing is known about the relations of occupational or other environmental factors to age at the final natural menstrual period and duration of the menopausal transition, occupational exposures and stressors (such as shift work, hours worked, hours spent standing, and heavy lifting) have been related to increased risk of adverse pregnancy outcomes132–135 and changes in menstrual cycle length and variability as well as fecundability.136–139 In addition, such environmental exposures as dichlorodiphenyltrichloroethane and polychlorinated biphenyls have been shown to have estrogenic activity and to be associated with an increased risk of breast cancer,140,141 although this association has not been consistently observed.142,143 Thus, the presumed endocrine effects of such exposures make it reasonable to expect that occupational and environmental exposures may be related to endocrine disruption that is reflected in altered age at natural menopause. One study showed a modest effect on age at natural menopause in women in Seveso, Italy, who were exposed to 2,3,7,8-tetrachlorobenzo-p-dioxin, a halogenated compound that may affect ovarian function, during a chemical plant explosion in 1976.144 Another study showed that exposure to 1,1-dichloro-2,2-bis(p-chlorophenyl) ethylene was also associated with earlier natural menopause.145

Physical activity

Physical activity is associated with a number of changes in hormonal parameters [estradiol, progesterone, prolactin, luteinizing hormone (LH), and FSH), both during and after intense physical activity.146–148 The concentrations of these hormones tend to be lower at rest among women who are physically active.146,147,149,150 Also, athletes tend to have a later age at menarche and increased occurrences of anovulation151 and amenorrhea152 and, among those who menstruate, a shortened luteal phase and reduced mean and peak progesterone levels.104,149 Although physical activity is associated with decreased concentrations of reproductive hormones and frequency of ovulation, few studies have examined the effect of exercise on age at natural menopause, although 1 modestly sized study reported no relationship,59 and 1 large study of Chinese women showed a later age at natural menopause associated with leisure time physical activity during adolescence and adulthood.94

Diet

One early study from Papua, New Guinea, suggested that malnourished women ceased menstruation about 4 years earlier than well-nourished women,153 consistent with other studies showing that women with greater weight62,69 and height89 may have a later age at natural menopause. Findings regarding the relationship of specific dietary patterns to age at menopause have been inconsistent. For example, vegetarians were observed to have an earlier age at natural menopause in 1 study,154 whereas another study in Japan reported that higher green and yellow vegetable intake was significantly associated with later age at natural menopause.155 Further, a large cross-sectional study of Japanese women found that higher intakes of fat, cholesterol, and coffee were significantly associated with earlier natural menopause after controlling for age, total energy, parity, menarche age, and relative weight.156 A longitudinal study of nearly 5000 German women observed that high carbohydrate consumption and high intake of vegetable, fiber, and cereal products were related to an earlier age at natural menopause, whereas higher intake of total fat, protein, and meat were associated with a later natural menopause.157 The large, prospective Shanghai Women’s Health Study found that higher total intake of calories, fruits, and protein was significantly associated with later age at natural menopause, whereas vegetable, fat, soy, and fiber intakes were not significantly related to age at menopause.94 Inclusion of meat in the diet of vegetarians has been observed to increase the episodic releases of LH and FSH and the length of the menstrual cycle.158 Thus, meat may modify the interaction of hormones along the hypothalamic-pituitary-ovarian axis. A couple of studies have reported that increased meat or alcohol consumption is significantly associated with later age at menopause, after adjusting for age and smoking.61,121 Dietary fiber (whose intake tends to be inversely related to meat intake) may interrupt enterohepatic circulation of sex hormones, leading to the lower circulating estrogen concentrations among vegetarian women.159 Nonetheless, a low-fat, high-carbohydrate intervention diet to prevent breast cancer in over 2600 women with extensive mammographic density followed for an average 7 years did not influence the timing of natural menopause, except a significantly earlier natural menopause was observed in those with low BMI who were on the intervention diet.160

Premenopausal women administered soy have shown increased plasma estradiol concentrations and follicular phase length, delayed menstruation, and suppressed midcycle surges of LH and FSH.161 Among postmenopausal women fed soy, FSH and LH did not decrease significantly, nor did sex hormone-binding globulin increase, and little change occurred in endogenous estradiol or body weight, although a small estrogenic effect on vaginal cytology was observed.162 However, the role of dietary fiber, phytoestrogens, fat, protein, and other nutrients in affecting age at menopause and duration of the perimenopause remains to be systematically studied, but has potentially important implications for prevention of chronic disease in midlife and older women.

CONCLUSION

Despite important methodologic differences, the limitations in the study designs used and the populations studied in the accumulating literature regarding factors that affect the age at which the natural final menstrual period is experienced, an interesting and complex picture is emerging. A number of demographic (eg, education, employment, race/ethnicity), menstrual and reproductive (eg, parity and OC use), familial and genetic, and lifestyle (eg, smoking, weight, physical activity and diet) factors seem to be important determinants of the age at which natural menopause occurs. Smoking, lower parity, and lower SES have been found fairly consistently to be associated with earlier menopause, an indicator of reduced longevity. However, the relationships with African American and Latina race/ethnicity, vegetarian diet, and undernutrition, body mass and composition, and physical activity have been inconsistent, possibly owing to varying methodologic approaches and limitations ().

Table 1

Factors related to earlier and later age at natural menopause

Factors Consistently Related to Earlier Age at Natural Menopause (References)Factors Inconsistently Related to Age at Natural Menopause (References)
Low socioeconomic status51–54,57,58,61,71,85–88Race/ethnicity58–60,80–84
Low/parity50–52,55,57,58,61,90,91,93,96Body mass index or body com position50–52,54,57,59,62,69,98–101
Not using oral contraceptives50,52,58,61,63,72,98Physical activity59,94
Active smoking50,51,55,57–59,61,63–69,86,96,121,124–126Dietary (vegetable, meat, fat, fiber) intake61,121,153–157,160

Other relationships remain largely unexplored (eg, passive smoke exposure and occupational and other environmental exposures). Therefore, much remains to be learned about how these factors affect follicular atresia and hormone levels and thus determine the onset and potentially the duration of the perimenopause and the timing of the final menstrual period. Furthermore, increased understanding of the underlying physiologic mechanisms of these influences needs to include potential genetic, metabolic, and racial/ethnic differences in physiologic responses to lifestyle factors and other environmental exposures and the interaction of genetic factors with these lifestyle and environmental factors. Increasing knowledge about these relationships ultimately offers women and their health care providers enhanced understanding and choices, based on greater knowledge, to deal with the individual presentations of menopause.

ACKNOWLEDGMENTS

The Study of Women’s Health Across the Nation (SWAN) has grant support from the National Institutes of Health (NIH), DHHS, through the National Institute on Aging (NIA), the National Institute of Nursing Research (NINR) and the NIH Office of Research on Women’s Health (ORWH) (Grants NR004061; AG012505, AG012535, AG012531, AG012539, AG012546, AG012553, AG012554, AG012495). Dr Gold was supported by AG012554. The content of this article is solely the responsibility of the author and does not necessarily represent the official views of the NIA, NINR, ORWH or the NIH.

REFERENCES

1. Cooper GS, Sandler DP. Age at natural menopause and mortality. Ann Epidemiol. 1998;8:229–35. [PubMed] [Google Scholar]2. Wise AM, Krajnak KM, Kashon ML. Menopause: the aging of multiple pacemakers. Science. 1996;273:67–70. [PubMed] [Google Scholar]3. Snowdon DA, Kane RL, Beeson WL, et al. Is early natural menopause a biologic marker of health and aging? Am J Public Health. 1989;79:709–14. [PMC free article] [PubMed] [Google Scholar]4. Ossewaarde ME, Bots ML, Verbeek ALM, et al. Age at menopause, cause-specific mortality and total life expectancy. Epidemiology. 2005;16:556–62. [PubMed] [Google Scholar]5. Jacobsen BK, Heuch I, Kvale G. Age at natural menopause and all-cause mortality: a 37-year follow-up of 19,731 Norwegian women. Am J Epidemiol. 2003;157:923–9. [PubMed] [Google Scholar]6. De Kleijn MJ, van der Schouw YT, Verbeek AL, et al. Endogenous estrogen exposure and cardiovascular mortality risk in postmenopausal women. Am J Epidemiol. 2002;155:339–45. [PubMed] [Google Scholar]7. Van der Schouw YT, van der Graaf Y, Steyerberg EW, et al. Age at menopause as a risk factor for cardiovascular mortality. Lancet. 1996;347:714–8. [PubMed] [Google Scholar]8. Jacobsen BK, Nilssen S, Heuch I, et al. Does age at natural menopause affect mortality from ischemic heart disease? J Clin Epidemiol. 1997;50:475–9. [PubMed] [Google Scholar]9. Hu FB, Grodstein F, Hennekens CH, et al. Age at natural menopause and risk of cardiovascular disease. Arch Intern Med. 1999;159:1061–6. [PubMed] [Google Scholar]10. Atsma F, Bartelink ML, Grobbec DE, et al. Postmenopausal status and early menopause as independent risk factors for cardiovascular disease: a meta-analysis. Menopause. 2006;13:265–79. [PubMed] [Google Scholar]11. Cui R, Iso H, Toyoshima H, et al. JACC Study Group. Relationships of age at menarche and menopause, and reproductive year with mortality from cardiovascular disease in Japanese postmenopausal women: the JACC study. J Epidemiol. 2006;16:177–84. [PMC free article] [PubMed] [Google Scholar]12. Jansen SC, Temme EH, Schouten EG. Lifetime estrogen exposure versus age at menopause as mortality predictor. Maturitas. 2002;43:105–12. [PubMed] [Google Scholar]13. Jacobsen BK, Knutsen SF, Fraser GE. Age at natural menopause and total mortality and mortality from ischemic heart disease: the Adventist Health Study. J Clin Epidemiol. 1999;52:303–7. [PubMed] [Google Scholar]14. Lisabeth LD, Beiser AS, Brown DL, et al. Age at natural menopause and risk of ischemic stroke The Framingham Heart Study. Stroke. 2009;40:1044–9. [PMC free article] [PubMed] [Google Scholar]16. Joakimsen O, Bonaa KH, Stensland-Bugge E, et al. Population-based study of age at menopause and ultrasound assessed carotid atherosclerosis: the Tromso Study. J Clin Epidemiol. 2000;53:525–30. [PubMed] [Google Scholar]17. Parazzini F, Bidoli E, Franceschi S, et al. Menopause, menstrual and reproductive history, and bone density in northern Italy. J Epidemiol Community Health. 1996;50:519–23. [PMC free article] [PubMed] [Google Scholar]18. Kritz-Silverstein D, Barrett-Connor E. Early menopause, number of reproductive years, and bone mineral density in postmenopausal women. Am J Public Health. 1993;83:983–8. [PMC free article] [PubMed] [Google Scholar]19. Van Der Voort DJ, Van Der Weijer PH, Barentsen R. Early menopause: increased fracture risk at older age. Osteoporos Int. 2003;14:525–30. [PubMed] [Google Scholar]20. Kelsey JL, Gammon MD, John EM. Reproductive factors and breast cancer. Epidemiol Rev. 1993;15:36–47. [PubMed] [Google Scholar]21. Monninkhof EM, van der Schouw YT, Peeters PH. Early age at menopause and breast cancer: are leaner women more protected? A prospective analysis of the Dutch DOM cohort. Breast Cancer Res Treat. 1999;55:285–91. [PubMed] [Google Scholar]22. De Graaff J, Stolte LA. Age at menarche and menopause of uterine cancer patients. Eur J Obstet Gynecol Reprod Biol. 1978;8:187–93. [PubMed] [Google Scholar]23. Franceschi S, La Vecchia C, Booth M, et al. Pooled analysis of 3 European case-control studies of ovarian cancer: II. Age at menarche and at menopause. Int J Cancer. 1991;49:57–61. [PubMed] [Google Scholar]24. Kaaks R, Lukanova A, Kurzer MS. Obesity, endogenous hormones, and endometrial cancer risk: a synthetic review. Cancer Epidemiol Biomarkers Prev. 2002;11:1531–43. [PubMed] [Google Scholar]25. Xu WH, Xiang YB, Ruan ZX, et al. Menstrual and reproductive factors and endometrial cancer risk: results from a population-based case-control study in urban Shanghai. Int J Cancer. 2004;108:613–9. [PubMed] [Google Scholar]26. Rivera CM, Grossardt BR, Rhodes DJ, et al. Increased cardiovascular mortality after early bilateral oophorectomy. Menopause. 2009;16:15–23. [PMC free article] [PubMed] [Google Scholar]27. Lokkegaard E, Jovanovic Z, Heitmann BL, et al. The association between early menopause and risk of ischaemic heart disease: influence of hormone therapy. Maturitas. 2006;53:226–33. [PubMed] [Google Scholar]28. Woods NF, Mitchell ES, Adams C. Memory functioning among midlife women: observations for the Seattle Midlife Women’s health Study. Menopause. 2000;7:257–65. [PubMed] [Google Scholar]29. Halbreich U, Piletz J, Halaris A. Influence of gonadal hormones on neurotransmitters, receptor, cognition and mood. Clin Neuropharmacol. 1992;15(Suppl A):590A–1A. [PubMed] [Google Scholar]30. Kok HS, Kuh D, Cooper R, et al. Cognitive function across the life course and the menopausal transition in a British birth cohort. Menopause. 2006;13:19–27. [PubMed] [Google Scholar]31. World Health Organization . Research on the menopause in the 1990s. World Health Organization; Geneva (Switzerland): 1996. [Google Scholar]32. Skolnick AA. At third meeting, menopause experts make the most of insufficient data. JAMA. 1992;268:2483–5. [PubMed] [Google Scholar]33. Avis NE, Kaufert PA, Lock M, et al. The evolution of menopausal symptoms. Baillieres Clin Endocrinol Metab. 1993;7:17–32. [PubMed] [Google Scholar]34. Cramer DW, Xu H. Predicting age at menopause. Maturitas. 1996;23:319–26. [PubMed] [Google Scholar]35. Hahn RA, Eaker E, Rolka H. Reliability of reported age at menopause. Am J Epidemiol. 1997;146:771–5. [PubMed] [Google Scholar]36. Sowers MF, LaPietra MT. Menopause: its epidemiology and potential association with chronic diseases. Epidemiol Rev. 1995;17:287–302. [PubMed] [Google Scholar]37. Gosden RG. Biology of the menopause: the causes and consequences of ovarian ageing. Academic Press; London: 1985. [Google Scholar]38. Burger HG, Dudley EC, Hopper JL. The endocrinology of the menopausal transition: a cross-sectional study of a population-based sample. J Clin Endocrinol Metab. 1995;80:3537–45. [PubMed] [Google Scholar]39. Soule MR, Bremner WJ. The menopause and climacteric: endocrinologic basis and associated symptomatology. J Am Geriatrics Soc. 1982;30:547. [PubMed] [Google Scholar]40. Thomford PJ, Jelovsek FR, Mattison DR. Effect of oocyte number and rate of atresia on the age of menopause. Repro Toxicol. 1987;1:41–51. [PubMed] [Google Scholar]41. Faddy MJ, Gosden RG, Gougeon A, et al. Accelerated disappearance of ovarian follicles in mid-life: implications for forecasting menopause. Hum Reprod. 1992;7:1342–6. [PubMed] [Google Scholar]43. Aydos SE, Elhan AH, Tukun A. Is telomere length one of the determinants of reproductive life span? Arch Gynecol Obstet. 2005;2727:113–6. [PubMed] [Google Scholar]44. Sherman BM, West JH, Korenman SG. The menopausal transition: analysis of LH, FSH, estradiol and progesterone concentrations during menstrual cycles of older women. J Clin Endocrinol Metab. 1976;42:629–36. [PubMed] [Google Scholar]45. Santoro N, Rosenberg-Brown J, Adel T, et al. Characterization of reproductive hormonal dynamics in the perimenopause. J Clin Endocrinol Metab. 1996;81:1495–1501. [PubMed] [Google Scholar]46. Upton GV. The perimenopause: physiologic correlates and clinical management. J Reprod Med. 1982;27:1–28. [PubMed] [Google Scholar]47. Shideler SE, DeVane GW, Kalra PS, et al. Ovarian pituitary hormone interactions during the menopause. Maturitas. 1989;11:331–9. [PubMed] [Google Scholar]48. Trevoux R, DeBrux J, Castaneir M, et al. Endometrium and plasma hormone profile in the peri-menopause and post-menopause. Maturitas. 1986;8:309–26. [PubMed] [Google Scholar]49. McKinlay SM, Brambilla DJ, Posner JG. The normal menopause transition. Maturitas. 1992;14:103–15. [PubMed] [Google Scholar]50. Greendale G, Hogan P, Kritz-Silverstein D, et al. Age at menopause in women participating in the postmenopausal estrogen/progestins interventions (PEPI) trial: an example of bias introduced by selection criteria. Menopause. 1995;2:27–34. for the PEPI trial investigators. [Google Scholar]51. Luoto R, Laprio J, Uutela A. Age at natural menopause and sociodemographic status in Finland. Am J Epidemiol. 1994;139:64–76. [PubMed] [Google Scholar]52. Stanford JL, Hartge P, Brinton LA, et al. Factors influencing the age at natural menopause. J Chron Dis. 1987;40:995–1002. [PubMed] [Google Scholar]53. Magursky V, Mesko M, Sokolik L. Age at the menopause and onset of the climacteric in women of Martin district, Czechoslovakia. Int J Fertil. 1975;20:17–23. [PubMed] [Google Scholar]54. Gold EB, Sternfeld B, Brown C, et al. The relation of demographic and lifestyle variables to symptoms in a multi-racial/ethnic population of women aged 40-55 years. Am J Epidemiol. 2000;152:463–73. [PubMed] [Google Scholar]55. van Noord PAH, Dubas JS, Dorland M, et al. Age at natural menopause in a population-based screening cohort: the role of menarche, fecundity, and lifestyle factors. Fertil Steril. 1997;68:95–102. [PubMed] [Google Scholar]56. Flint M. Is there a secular trend in age of menopause. Maturitas. 1978;1:133–9. [PubMed] [Google Scholar]57. Rodstrom K, Bengtsson C, Milsom I, et al. Evidence for a secular trend in menopausal age: a population study of women in Gothenburg. Menopause. 2003;10:538–43. [PubMed] [Google Scholar]58. Gold EB, Bromberger J, Crawford S, et al. Factors associated with age at menopause in a multi-ethnic population of women. Am J Epidemiol. 2001;153:865–74. [PubMed] [Google Scholar]59. Bromberger JT, Matthews KA, Kuller LH, et al. Prospective study of the determinants of age at menopause. Am J Epidemiol. 1997;145:124–33. [PubMed] [Google Scholar]60. Alvarado G, Rivera R, Ruiz R, et al. Characteristicas del patron de sangrado menstrual en un grupo de mujeres normales de Durango. Ginecol Obstetr Mex. 1988;56:127–33. [PubMed] [Google Scholar]61. Torgerson DJ, Avenell A, Russell IT, et al. Factors associated with onset of menopause in women aged 45-49. Maturitas. 1994;19:83–92. [PubMed] [Google Scholar]62. MacMahon B, Worcester J. Age at menopause, United States 1960-1962. Vital Health Stat. 1966;19:1–19. [PubMed] [Google Scholar]63. Palmer JR, Rosenberg L, Wise LA, et al. Onset of natural menopause in African American women. Am J Public Health. 2003;93:299–306. [PMC free article] [PubMed] [Google Scholar]64. McKinlay SM, Bifano NL, McKinlay JB. Smoking and age at menopause in women. Ann Intern Med. 1985;103:350–6. [PubMed] [Google Scholar]65. Andersen FS, Transbol I, Christiansen C. Is cigarette smoking a promoter of the menopause. Acta Med Scand. 1982;212:137–9. [PubMed] [Google Scholar]66. Hiatt RA, Fireman BH. Smoking, menopause, and breast cancer. J Natl Cancer Inst. 1986;76:833–8. [PubMed] [Google Scholar]67. Hartz AJ, Kelber S, Borkowf H, et al. The association of smoking with clinical indicators of altered sex steroids—a study of 50,145 women. Pub Health Rep. 1987;102:254–9. [PMC free article] [PubMed] [Google Scholar]68. Brambilla DJ, McKinlay SM. A prospective study of factors affecting age at menopause. J Clin Epidemiol. 1989;42:1031–9. [PubMed] [Google Scholar]69. Willett W, Stampfer MJ, Bain C, et al. Cigarette smoking, relative weight and menopause. Am J Epidemiol. 1983;117:651–8. [PubMed] [Google Scholar]70. Snieder H, MacGregor AJ, Spector ID. Genes control cessation of a woman’s reproductive life: a twin study of hysterectomy and age at menopause. J Clin Endocrinol Met. 1998;83:1875–80. [PubMed] [Google Scholar]71. Castelo-Branco C, Blümel JE, Chedraui P, et al. Age at menopause in Latin America. Menopause. 2006;13:706–12. Erratum in: Menopause 2006;13:850. [PubMed] [Google Scholar]72. Gonzales GF, Villena A. Age at menopause in central Andean Peruvian women. Menopause. 1997;4:32–8. [Google Scholar]73. McCarthy T. The prevalence of symptoms in menopausal women in the Far East: Singapore segment. Maturitas. 1994;19:199–204. [PubMed] [Google Scholar]74. Samil RS, Wishnuwardhani SD. Health of Indonesian women, city-dwellers of perimenopausal age. Maturitas. 1994;19:191–7. [PubMed] [Google Scholar]75. Wasti S, Robinson SC, Akhtar Y, et al. Characteristics of menopause in three groups in Karachi, Pakistan. Maturitas. 1993;16:61–9. [PubMed] [Google Scholar]76. Blumel J, Cubillos M, Brandt A, et al. Some clinical aspects of menopause. Rev Chil Obstet Ginecol. 1988;53:278–82. [PubMed] [Google Scholar]77. Kapoor AK, Kapoor S. The effects of high altitude on age at menarche and menopause. J Biometeor. 1986;30:21–6. [PubMed] [Google Scholar]78. Beall CM. Ages at menopause and menarche in a high altitude Himalayan population. Ann Hum Biol. 1983;10:365–70. [PubMed] [Google Scholar]79. Flint MP. PhD dissertation. City University of New York; 1974. Menarche and menopause in Rajput women. [Google Scholar]80. Otolorin EO, Adeyefa I, Osotimehin BO, et al. Clinical, hormonal and biochemical features of menopausal women in Ibadan, Nigeria. Afr J Med Sci. 1989;18:251–5. [PubMed] [Google Scholar]81. Beyene Y. Cultural significance and physiological manifestations of menopause, a bicultural analysis. Culture Med Psychiatr. 1986;10:47–71. [PubMed] [Google Scholar]82. Boulet M. The menopause and the climacteric in seven Asian countries. In: Sixth International Congress on the Menopause. Parthenon; New Jersey: 1990. [Google Scholar]83. Chompootweep S, Tankeyoon M, Yamarat K, et al. The menopausal age and climacteric complaints in Thai women in Bangkok. Maturitas. 1993;17:63–71. [PubMed] [Google Scholar]84. Ramoso-Jalbuena J. Climacteric Filipino women: a preliminary survey in the Philippines. Maturitas. 19:183–90. [PubMed] [Google Scholar]85. Lawlor DA, Ebrahim S, Smith GD. The association of socio-economic position across the life course and age at menopause: the British Women’s Heart and Health Study. Br J Obstet Gynecol. 2003;110:1078–87. [PubMed] [Google Scholar]86. Santoro N, Brockwell S, Johnston J, et al. Helping midlife women predict the onset of the final menses: SWAN, the Study of Women’s Health Across the Nation. Menopause. 2007;14:415–24. [PubMed] [Google Scholar]87. Hardy R, Kuh D. Social and environmental conditions across the life course and age at menopause in a British birth cohort study. BJOG. 2005;112:346–54. [PubMed] [Google Scholar]88. Mishra G, Hardy R, Kuh D. Are the effects of risk factors for timing of menopause modified by age? Results from a British birth cohort study. Menopause. 2007;14:717–24. [PubMed] [Google Scholar]89. Brand PC, Lehert PH. A new way of looking at environmental variables that may affect the age at menopause. Maturitas. 1978;1:121–32. [PubMed] [Google Scholar]90. McKinlay S, Jefferys M, Thompson B. An investigation of the age at menopause. J Biosoc Sci. 1972;4:161–73. [PubMed] [Google Scholar]91. Whelan EA, Sandler DP, McConnaughey DR, et al. Menstrual and reproductive characteristics and age at natural menopause. Am J Epidemiol. 1990;131:625–32. [PubMed] [Google Scholar]92. Treloar AE, Boynton RE, Behn BG, et al. Variation of the human menstrual cycle through reproductive life. Int J Fertil. 1966;12(Pt 2):77–126. [PubMed] [Google Scholar]93. Soberon J, Calderon JJ, Goldzieher JW. Relation of parity to age at menopause. Am J Obstet Gynecol. 1966;96:96–100. [PubMed] [Google Scholar]94. Dorjgochoo T, Kallianpur A, Gao Y-T, et al. Dietary and lifestyle predictors of age at natural menopause and reproductive span in the Shanghai Women’s Health Study. Menopause. 2008;15:924–33. [PMC free article] [PubMed] [Google Scholar]95. Loh FH, Khin LW, Saw SM, et al. The age of menopause and the menopause transition in a multiracial population: a nation-wide Singapore study. Maturitas. 2005;52:169–80. [PubMed] [Google Scholar]96. Reynolds RF, Obermeyer CM. Age at natural menopause in Spain and the United States: results from the DAMES project. Am J Hum Biol. 2005;17:331–40. [PubMed] [Google Scholar]97. Parazzini F, Negri E, LaVecchia C. Reproductive and general lifestyle determinants of age at menopause. Maturitas. 1992;15:141–9. [PubMed] [Google Scholar]98. van Keep PA, Brand PC, Lehert PH. Factors affecting the age at menopause. J Biosoc Sci Suppl. 1979;6:37–55. [PubMed] [Google Scholar]99. Lindquist O, Bengtsson C. Menopausal age in relation to smoking. Acta Med Scand. 1979;205:73–7. [PubMed] [Google Scholar]100. Daniell HWP. Smoking, obesity, and the menopause. Lancet. 1978;2:373. [PubMed] [Google Scholar]101. den Tonkelaar I, Seidell J. Fat distribution in relation to age, degree of obesity, smoking habits, parity and estrogen use: a cross-sectional study of 11,825 Dutch women participating in the DOM project. Int J Obesity. 1990;14:753–61. [PubMed] [Google Scholar]103. Kaye S, Folsom A, Prineas RJ, et al. The association of body fat distribution with lifestyle and reproductive factors in a population study of postmenopausal women. Int J Obesity. 1990;14:583–91. [PubMed] [Google Scholar]104. Kok HS, van Asselt KM, van der Schouw YT, et al. Genetic studies to identify genes underlying menopause age. Hum Reprod Update. 2005;11:483–93. [PubMed] [Google Scholar]105. Van Asselt KM, Kok HS, Pearson PL, et al. Heritability of menopausal age in mothers and daughters. Fertil Steril. 2004;82:1348–51. [PubMed] [Google Scholar]106. Torgerson DJ, Thomas RE, Reid DM. Mothers and daughters menopausal ages: is there a link? Eur J Obstet Gynecol Reprod Biol. 1997;74:63–6. [PubMed] [Google Scholar]107. Cramer DW, Xu H, Harlow BL. Family history as a predictor of early menopause. Fertil Steril. 1995;64:740–5. [PubMed] [Google Scholar]108. DeBruin JP, Bovenhuis H, VanNoord PA, et al. The role of genetic factors in age at natural menopause. Hum Reprod. 2001;16:2014–8. [PubMed] [Google Scholar]109. Murabito JM, Yang Q, Fox C, et al. Heritability of age at natural menopause in the Framingham Heart Study. J Clin Endocrinol Metab. 2005;90:3427–30. [PubMed] [Google Scholar]110. Stolk L, Zhai G, Van Meurs JB, et al. Loci at chromosomes 13, 19 and 20 influence age at natural menopause. Nat Genet. 2009;41:645–7. [PMC free article] [PubMed] [Google Scholar]111. Weel AE, Uitterlinden AG, Westendorp IC, et al. Estrogen receptor polymorphism predicts the onset of natural and surgical menopause. J Clin Endocrinol Metab. 1999;84:3146–50. [PubMed] [Google Scholar]112. He C, Kraft P, Chen C, et al. Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. Nat Genet. 2009;41:724–8. [PMC free article] [PubMed] [Google Scholar]113. He C, Kraft P, Chasman DI, et al. A large-scale candidate gene association study of age at menarche and age at natural menopause. Hum Genet. 2010;128:515–27. [PMC free article] [PubMed] [Google Scholar]114. Lu Y, Liu P, Recker RR, et al. TNFRSF11A and TNFSF11 are associated with age at menarche and natural menopause in white women. Menopause. 2010;17:1048–54. [PMC free article] [PubMed] [Google Scholar]115. Hardy R, Kuh D. Does early growth influence timing of the menopause? Evidence from a British birth cohort. Hum Reprod. 2002;17:2474–9. [PubMed] [Google Scholar]116. Cresswell JL, Egger P, Fall CH, et al. Is the age of menopause determined in-utero? Early Hum Dev. 1997;49:143–8. [PubMed] [Google Scholar]117. Treloar SA, Sadrzadeh S, Do KA, et al. Birth weight and age at menopause in Australian female twin pairs: exploration of the fetal origin hypothesis. Hum Reprod. 2000;15:55–9. [PubMed] [Google Scholar]118. Kuh D, Butterworth S, Kok H, et al. Childhood cognitive ability and age at menopause: evidence from two cohort studies. Menopause. 2005;12:475–82. [PubMed] [Google Scholar]119. Richards M, Kuh D, Hardy R, et al. Lifetime cognitive function and timing of the natural menopause. Neurology. 1999;53:308–14. [PubMed] [Google Scholar]120. Whalley LJ, Fox HC, Starr JM, et al. Age at natural menopause and cognition. Maturitas. 2004;49:148–56. [PubMed] [Google Scholar]121. Kinney A, Kline J, Levin B. Alcohol, caffeine and smoking in relation to age at menopause. Maturitas. 2006;54:27–38. [PubMed] [Google Scholar]122. McKinlay SM, Brambilla DJ, Posner JG. The normal menopause transition. Maturitas. 1992;14:103–15. [PubMed] [Google Scholar]123. Adena MA, Gallagher HG. Cigarette smoking and the age at menopause. Ann Human Biol. 1982;9:121–30. [PubMed] [Google Scholar]124. Jick H, Porter J, Morrison AS. Relation between smoking and age of natural menopause. Lancet. 1977;1:1354–5. [PubMed] [Google Scholar]125. Midgett AS, Baron JA. Cigarette smoking and the risk of natural menopause. Epidemiol. 1990;1:464–80. [Google Scholar]126. Mattison DR, Thorgierssen SS. Smoking and industrial pollution and their effects on menopause and ovarian cancer. Lancet. 1978;1:187–8. [PubMed] [Google Scholar]127. Essenberg JM, Fagan L, Malerstein AJ. Chronic poisoning of the ovaries and testes of albino rats and mice by nicotine and cigarette smoke. West J Surg Obstet Gynecol. 1951;59:27–32. [PubMed] [Google Scholar]129. Michnovicz J, Hershcopf R, Naganuma H, et al. Increased 2-hydroxylation of estradiol as a possible mechanism for the anti-estrogenic effect of cigarette smoking. N Engl J Med. 1986;315:1305–9. [PubMed] [Google Scholar]130. Krailo MD, Pike MC. Estimation of the distribution of the age at natural menopause from prevalence data. Am J Epidemiol. 1983;117:356–61. [PubMed] [Google Scholar]131. Everson RB, Sandler DP, Wilcox AJ, et al. Effect of passive exposure to smoking on age at natural menopause. Br Med J. 1986;293:792. [PMC free article] [PubMed] [Google Scholar]132. Mamelle N, Laumon B, Lazar P. Prematurity and occupational activity during pregnancy. Am J Epidemiol. 1984;119:309–22. [PubMed] [Google Scholar]134. Beaumont JJ, Swan SH, Hammond SK, et al. Historical cohort investigation of spontaneous abortion in the Semiconductor health Study: methods and analyses of risk in fabrication overall and in fabrication work groups. Am J Ind Med. 1995;28:735–50. [PubMed] [Google Scholar]135. Swan SH, Beaumont JJ, Hammond SK, et al. Historical cohort study of spontaneous abortion among fabrication workers in the Semiconductor Health Study; agent-level analysis. Am J Ind Med. 1995;28:751–70. [PubMed] [Google Scholar]137. Messing K, Saurel-Cubizolles MG, Bourgine M, et al. Menstrual cycle characteristics and work condition of workers in poultry slaughterhouses and canneries. Scand J Work Environ Health. 1992;18:302–9. [PubMed] [Google Scholar]138. Eskenazi B, Gold EB, Samuels SJ, et al. Prospective assessment of fecundability of female semiconductor workers. Am J Ind Med. 1995;28:817–32. [PubMed] [Google Scholar]139. Gold EB, Eskenazi B, Hammond SK, et al. Prospectively assessed menstrual cycle characteristics in female wafer-fabrication and nonfabrication semiconductor employees. Am J Ind Med. 1995;28:799–816. [PubMed] [Google Scholar]140. Falck F, Jr, Ricci A, Jr, Wolff MS, et al. Pesticides and polychlorinated biphenyl residues in human breast lipids and their relation to breast cancer. Arch Environ Health. 1992;47:143–6. [PubMed] [Google Scholar]141. Wolff MS, Toniolo PG, Lee EW, et al. Blood levels of organochlorine residues and risk of breast cancer. J Natl Cancer Inst. 1993;85:648–52. [PubMed] [Google Scholar]142. Krieger N, Wolff MS, Hiatt RA, et al. Breast cancer and serum organochlorines: a prospective study among white, black and Asian women. J Natl Cancer Inst. 1994;86:589–99. [PubMed] [Google Scholar]143. Hunter DJ, Hankinson SE, Laden F, et al. Plasma organochlorine levels and risk of breast cancer. N Engl J Med. 1997;337:1253–8. [PubMed] [Google Scholar]144. Eskenazi B, Warner M, Marks AR, et al. Serum dioxin concentrations and age at menopause. Environ Health Perspect. 2005;113:858–62. [PMC free article] [PubMed] [Google Scholar]145. Cooper GS, Savitz DA, Millikan R, et al. Organochlorine exposure and age at natural menopause. Epidemiol. 2002;13:729–33. [PubMed] [Google Scholar]146. Cummings SR, Kelsey J, Nevitt MC, et al. Epidemiology of osteoporosis and osteoporotic fractures. Epidemiol Rev. 1985;7:178–208. [PubMed] [Google Scholar]147. Bonen A, Ling WH, Belcastro AN, et al. Profiles of selected hormones during menstrual cycles of teenage athletes. J Appl Physiol. 1981;50:545–51. [PubMed] [Google Scholar]148. Jurkowski JE, Joanes NL, Walker C, et al. Ovarian hormonal responses to exercise. J Appl Physiol. 1978;44:109–14. [PubMed] [Google Scholar]149. Loucks AB, Mortola LF, Girtoon L, et al. Alterations in the hypothalamic-pituitary-ovarian and the hypothalamic-pituitary-adrenal axes in athletic women. J Clin Endocrinol Metab. 1989;68:402–11. [PubMed] [Google Scholar]150. Jasienska G, Ziomkiewicz A, Thune I, et al. Habitual physical activity and estradiol levels in women of reproductive age. Eur J Cancer Prev. 2006;15:439–45. [PubMed] [Google Scholar]151. Bernstein L, Ross RK, Lobo RA, et al. The effects of moderate physical activity on menstrual cycle patterns in adolescence: implications for breast cancer prevention. Br J Cancer. 1987;55:681–5. [PMC free article] [PubMed] [Google Scholar]152. Loucks AB, Horvath SM. Athletic amenorrhea: a review. Med Sci Sports Exer. 1985;17:56–72. [PubMed] [Google Scholar]153. Scragg RFR. Menopause and reproductive span in rural Nuigini. Proc Ann Symp Papua New Guinea Med Soc. 1973:126–44. [Google Scholar]154. Baird DD, Trlavsky FA, Anderson JJB. Do vegetarians have earlier menopause? Proc Soc Epidemiol Res. 1988:907–8. [Google Scholar]155. Nagata C, Takatsuka N, Kawakami N, et al. Association of diet with the onset of menopause in Japanese women. Am J Epidemiol. 2000;152:863–7. [PubMed] [Google Scholar]156. Nagata C, Takatsuka N, Inaba S, et al. Association of diet and other lifestyle with onset of menopause in Japanese women. Maturitas. 1998;29:105–13. [PubMed] [Google Scholar]157. Nagel G, Altenburg HP, Nieters A, et al. Reproductive and dietary determinants of the age at menopause in EPIC-Heidelberg. Maturitas. 2005;52:337–47. [PubMed] [Google Scholar]158. Hill PB, Garbaczewski L, Daynes G, et al. Gonadotrophin release and meat consumption in vegetarian women. Am J Clin Nutr. 1986;43:37–41. [PubMed] [Google Scholar]159. Adlercreutz H, Mousavi Y, Loukovaara M, et al. Lignans, isoflavones, sex hormone metabolism and breast cancer. In: Hochberg R, Naftolin F, editors. The new biology of steroid hormones. Raven Press; New York: 1992. pp. 145–54. [Google Scholar]160. Martin LJ, Greenberg CV, Kriukov V, et al. Intervention with a low-fat, high-carbohydrate diet does not influence the timing of menopause. Am J Clin Nutr. 2006;84:920–8. [PubMed] [Google Scholar]161. Cassidy A, Bingham S, Setchell KDR. Biological effects of a diet of soy protein rich in isoflavones on the menstrual cycle of premenopausal women. Am J Clin Nutr. 1994;60:333–40. [PubMed] [Google Scholar]162. Baird DD, Umbach DM, Lansdell L, et al. Dietary intervention study to assess estrogenicity of dietary soy among postmenopausal women. J Clin Endocrinol Metab. 1995;80:1685–90. [PubMed] [Google Scholar]

Symptoms, Treatments, Weight Gain, and More

 

Perimenopause, or menopause transition, begins several years before menopause. It’s the time when the ovaries gradually begin to make less estrogen. It usually starts in women’s 40s, but can start in their 30s or even earlier.

Perimenopause lasts up until menopause, the point when the ovaries stop releasing eggs. In the last 1 to 2 years of perimenopause, this drop in estrogen speeds up. At this stage, many women have menopause symptoms.

How Long Does Perimenopause Last?

The average length of perimenopause is 4 years, but for some women this stage may last only a few months or continue for 10 years. Perimenopause ends when women have gone 12 months without having their period.

What Are the Signs of Perimenopause?

Women in perimenopause have at least some these symptoms:

Are My Perimenopausal Symptoms Normal or Something to Be Concerned About?

Irregular periods are common and normal during perimenopause. But other conditions can cause changes in menstrual bleeding. If any of the following situations apply to you, see a doctor to rule out other causes:

  • Your periods are very heavy, or they have blood clots.
  • Your periods last several days longer than usual.
  • You spot between periods.
  • You have spotting after sex.
  • Your periods happen closer together.

Causes of abnormal bleeding include hormone problems, birth control pills, pregnancy, fibroids, blood clotting problems or, rarely, cancer.

How Is Perimenopause Diagnosed?

Often your doctor can make the diagnosis of perimenopause based on your symptoms. A blood test to check hormone levels may also help, but your hormone levels are changing during perimenopause. It may be more helpful to have several blood tests done at different times for comparison.

Can I Get Pregnant If I Am Perimenopausal?

Yes. Despite a decline in fertility during the perimenopause stage, you can still become pregnant. If you do not want to become pregnant, you should use some form of birth control until you reach menopause (you have gone 12 months without having your period).

For some women, getting pregnant can be difficult once they are in their late 30s to early 40s due to a drop in fertility. If becoming pregnant is the goal, there are treatments that can help you get pregnant.

Are There Treatments That Can Ease the Symptoms of Perimenopause?

Many women get relief from hot flashes after taking low-dose birth control pills for a short time. Other options that may control hot flashes include the birth control skin patch, vaginal ring, and progesterone injections. Certain women should not use birth control hormones, so talk to your doctor to see if they are right for you.

You may also feel better if you do things that enhance your general well-being, such as:

  • Exercise.
  • Stop smoking.
  • Get more sleep and try going to sleep and waking up at the same time each day.
  • Drink less alcohol.
  • Get to a healthy weight and stay there.
  • Get enough calcium in your diet.
  • Ask your doctor if you should take a multivitamin.

Talk to your doctor if you are having problems with your sex drive. They may be able to recommend a counselor or therapist to help you and your partner work through this problem. Vaginal lubricants may also be recommended, if vaginal dryness is a problem.

Other treatments available to help with the various symptoms of perimenopause may include antidepressant medications for mood swings.

Talk to your doctor about your specific symptoms and goals of treatment. This will help them make a plan that is right for you.

 

Menopause | Penn Center for Women’s Behavioral Wellness

  • Home
  • Behavioral Wellness At Any Age
  • Menopause
Make an Appointment

Please see our contact page to make an appointment or contact our Patient Services Manager at 215-573-8886 or email us for more information. 

Menopause

Menopause is a natural event that happens in every woman’s life. The average age for menopause in the United States is approximately 52 years, but the menopause transition can last for a number of years. During the menopause transition, women’s ovaries produce less and less of the hormone estrogen, until menses stops completely. The loss of estrogen may cause hot flashes, night sweats, insomnia, headaches, irregular periods, and vaginal dryness. In addition, some menopausal women experience moodiness, an inability to concentrate, forgetfulness, trouble being organized and are easily distracted.



The “Menopause Transition”

There are various stages in the menopause transition. Women proceed from being premenopausal to postmenopausal over several years. Some women “go through the menopause” earlier and/or more quickly than others just as some women have bothersome symptoms while others do not. Several large studies of women from across the United States have suggested the following “stages” for the menopause transition.

  • Premenopause: There is no change in cycle length and a woman can predict when she will get her period.
  • Early Transition: There is a decrease in predictability regarding when a woman will get her period because her cycles are no longer the same length each month. Some women may be able to predict their menstrual cycle for several months, but the length of their “usual” cycle has changed by several days.
  • Late Transition: A woman has experience 2-11 months without a period.
  • Postmenopause: A woman has not had a period in 12 months.

Many women wonder what is happening to their hormones during the menopause. Each month from the time of puberty to menopause, a woman’s ovaries are stimulated by a hormone made in the brain called follicular stimulating hormone (FSH). FSH causes ovarian follicles to enlarge and produce estrogen. Over time, fewer and fewer follicles remain to be stimulated and thus estrogen levels decline as a woman ages. This decline in estrogen leads to an increase in FSH as there is not enough estrogen being produced to “turn off” the brain’s production of FSH. FSH is sometimes used as a measure of whether a woman is peri or postmenopausal. An FSH level of > 30 IU/L is consistent with the perimenopause, although FSH levels of 70-90 IU/L are not uncommon for postmenopausal women. Many gynecologists base their decision about whether someone is peri or postmenopausal on the woman’s menstrual history and the presence of common menopausal symptoms. The FSH test is not considered diagnostic for the menopause. Sometimes women in the early stages of the menopause transition can actually have high estrogen levels because that month the follicles she has remaining in her ovaries were able to responded to the high levels of FSH and produce more estrogen. Thus, the menopause can be characterized by very high and very low levels of estrogen.


Natural versus Surgical Menopause

Treatments for Menopause Related Symptoms
  • Hormone Therapy
  • Botanical Supplements
  • Antidepressants
  • Sleep Medications

Dealing With Rage During the Perimenopause Transition and Beyond

The rage hit Juliet Doherty like a train. At 48 years old, Doherty had been in perimenopause for two years, living with daily headaches, sore breasts and irregular periods. But it had been manageable.

“Naively, I believed that if that was all it was, I would be fine,” Doherty said.

That suddenly changed when she began to experience anger unlike any she’d experienced before.

“Emotionally, I was a wreck,” Doherty recalled. “My life spiraled out of control . . . It was like watching a car crash and you couldn’t stop it.”

She described her anger as “the rage”: an intense burning in her stomach that didn’t cease until it was released. She lashed out at family, friends — she even broke an electric fan. Afterward, she’d cry, frustrated from losing control.

Where does this anger come from?

Though menopause gets all the attention, it’s even more common for women to experience mood changes during perimenopause — the transitional period before menopause that’s marked by hormone fluctuation, inconsistent ovulation and irregular periods. (Some people will experience mood swings and increased risk of developing depression in the early postmenopausal period too.) Menopause isn’t reached until a year after the last normal period, which occurs, on average, at the age of 51 in the U.S. Perimenopause, however, can last anywhere from four to 10 years, and begin as early as your 30s.

“Perimenopause is a time of vulnerability for women due to hormone fluctuation,” Dr. JoAnn Pinkerton, medical director of Midlife Health Center and a member of HealthyWomen’s Women’s Health Advisory Council, told HealthyWomen.

She explained that overwhelming rage, much like what Doherty experienced, may be related to the body’s changes in estrogen levels — specifically estradiol –– in combination with stressors. During the course of perimenopause, estrogen continues to fluctuate, which also affects other hormones (like serotonin and oxytocin), and frequently leaves the body with either too many or too few hormones at any given time.

Mood swings, if they’re experienced, are often triggered by the body’s sensitivity to this fluctuation. But, because of the constant shift, Pinkerton explained, it’s not uncommon for feelings of rage to last a week or two and then disappear as the body adjusts.

According to Dr. Sheryl Kingsberg, a professor of reproductive biology and psychiatry at Case Western Reserve University and a member of HealthyWomen’s Women’s Health Advisory Council, poor sleep can also be a factor in mood swings.

“[During perimenopause], the decrease in estrogen is the cause of an increase in hot flashes and night sweats, [which can disrupt sleep],” Kingsberg said, adding that the shift in hormones may actually disrupt sleep itself, even without hot flashes.

Risk of depression

“Twenty-six to 33% of women exhibit significant depressive symptoms during this hormonal flux,” Pinkerton said.

For women, who are nearly twice as likely as men to be diagnosed with depression, depressive episodes are often linked to hormonal life events such as perimenopause (as well as post-pregnancy and puberty).

If left untreated, anger during this transition can increase one’s risk of developing depression. Women with a history of pre-perimenopause depression or who’ve had a history of hormone-related mood changes, such as premenstrual dysphoric disorder, are at an even greater risk, Kingsberg explained.

Both doctors stressed that if you’re overwhelmed with feelings of rage, or rage is affecting your relationships, it’s important to seek help so that it doesn’t lead to depression.

Taming the rage

There are a number of perimenopause treatments available. According to Kingsberg, mood changes are looked at from a biopsychosocial perspective — the interconnection of biology, psychology and socioenvironmental factors. Pharmacological options include hormone replacement therapy (HRT) and low-dose antidepressants.

“There is no data that says hormones will treat major depression,” Kingsberg said, “But we certainly can use them for mild mood changes. We know that it can help.”

Hormones and antidepressants can provide a dual function: shift neurotransmission to restore mood and help reduce hot flashes. But HRT isn’t the only option, and it may not be the right option for everyone. (Kingsberg stressed the importance of talking to your OB-GYN for shared decision-making.)

Cognitive behavioral therapy (CBT) is another effective mode of addressing perimenopausal mood changes. This popular type of talk therapy, which provides tools to shift thought patterns away from the negative and back toward the neutral and positive, is often used for depression and can address irritability. According to Kingsberg, some CBT can help with insomnia and also reduce the intensity and frequency of hot flashes.

Because estradiol fluctuations make women more sensitive to stress, Pinkerton said, experiencing stressful life events during the perimenopausal transition heightens the risk of developing depression. Therefore, it’s important that women assess current life stressors to identify triggers. CBT and other mindfulness tools such as meditation can help women have a less negative emotional reaction to stress, which can decrease the development of depression.

“Mindfulness and the ability to step back are really important,” Pinkerton said.

Mediation, exercise and creative outlets are all useful activities to decrease stress and irritability. But most important — especially during the COVID-19 pandemic, which has greatly increased stressors — is that it’s crucial for anyone going through perimenopause who’s feeling especially overwhelmed (or experiencing other physical symptoms such difficulty sleeping, loss of sex drive or pain with intercourse) to reach out for help.

Doherty finally sought help after she climbed a ladder to yell at her neighbors for painting her fence.

“I realized I had lost control of my emotions, and I called my doctor,” Doherty explained.

She was put on HRT and her mood instantly changed. Today, she feels more in control of her life and emotions. Her headaches and hot flashes have also stopped.

“I am usually a very controlled, level-headed person. This hit me like lightning –– it was so fast,” Doherty said. “HRT has definitely helped control my symptoms. I don’t want to feel like that again.”

Resources:

Substance Abuse and Mental Health Services Administration National Helpline: 1-800-662-4357

National Suicide Prevention Lifeline: 1-800-273-8255

What To Expect When You’re Expecting Perimenopause — Sharp Health News

Jan. 27, 2016

There are commercials about it, ads in magazines about it, even skits on “Saturday Night Live” about it. We hear about menopause more often than we’d like, especially if we’re fast approaching it. But what we don’t often learn about is perimenopause, the period preceding menopause that lasts four years, on average.

Dr. Catherine Sundsmo, a family medicine doctor with Sharp Rees-Stealy, recently took some time to explain perimenopause and all that comes with it. Here are her top five tips on what to expect when you’re expecting perimenopause:

  1. Expect to wait a while. Natural menopause is defined as the permanent cessation of menstrual periods, determined after a woman has experienced 12 months of no menstrual periods. The average age of menopause is 51. Once menopause is complete, a woman can no longer get pregnant. Perimenopause, now commonly known as menopausal transition, occurs during the approximately four years preceding menopause.
  2. Expect those dreaded night sweats. Menopause does not happen suddenly. Many women experience several years of changes during the menopausal transition before their periods stop completely. The natural decline in estrogen in the body during perimenopause can cause symptoms such as hot flashes, night sweats, drastic mood changes, depression, anxiety, weight gain, forgetfulness, insomnia, exhaustion, headaches, irregular periods, breast pain, decreased libido and vaginal dryness. Many of these symptoms improve once the menopausal transition is complete, but some symptoms may persist.
  3. Expect that you might need a little help. Perimenopause and menopause are a normal part of a woman’s life and do not need to be treated medically. However, if symptoms are bothersome to you and disrupting your life, there are several treatments available. Some include anti-depressants, supplements, hormonal medications such as low-dose birth control or low-dose hormone therapy, and “natural” remedies such as black cohosh and soy.
  4. Expect to feel like you’re pregnant (even if you’re not). Perimenopause and pregnancy share several of the same symptoms including lack of periods, vaginal bleeding or spotting, weight gain, breast tenderness, headache and nausea. Even though the chance of getting pregnant between the ages of 45 to 49 is roughly 3 percent, the possibility of pregnancy must always be considered in any female who is experiencing these symptoms, is sexually active and does not use regular contraception.
  5. Expect to stay active. Although several factors such as genetics, smoking, obesity, ethnicity and reproductive history contribute to when you might see signs of perimenopause, there are things you can do to make the transition more comfortable. Exercise regularly to maintain cardiovascular health and weight, and to strengthen your pelvic floor muscles; enjoy a nutritious diet; drink lots of water to stay hydrated; practice relaxation methods to decrease stress; take 1,200 mg calcium and 800 to 2,000 IU vitamin D daily; and use a lubricant to ease intercourse discomfort.

Talk with your doctor if you have concerns about menopause. Together you can plan appropriate ways to address your symptoms.

90,000 signs, symptoms, age of onset. Menopause treatment in Moscow – Gineko – gynecological clinic

Menopause or menopause is a stage in a woman’s life when menstrual cycles gradually disappear and the body is no longer capable of ovulation and pregnancy. Menopause is characterized by a slow metabolism, as well as a decrease in the concentration of estrogens produced by the female sex glands. In most cases, the initial signs of menopause occur around 50 years of age.The last menstrual period before menopause is called menopause.

Every woman experiences menopause differently. For example, some ladies suffer from a wide range of very unpleasant manifestations of menopause: pronounced mood swings, “hot flashes”, painful sensations in the lower abdomen, insufficient vaginal lubrication. Other women hardly notice any unpleasant manifestations during the climacteric period.

The term “climacteric (menopausal) syndrome” is used to denote the pathological and painful course of menopause.This syndrome causes not only discomfort and a decrease in the quality of life. It often signals a serious malfunction of the endocrine, circulatory and nervous systems, requiring immediate attention from a gynecologist. With the onset of menopause, the risk of developing neoplasms of the female genital area, for example, cancer of the ovaries, uterus and mammary glands, also increases.

Reasons

The ovaries of young women synthesize the amount of estrogen sufficient for the normal course of menstruation and other natural processes in a woman’s body.At about the age of 40, natural age-related changes occur in the ovaries, and they begin to produce less and less estrogen. The ovaries gradually decrease in size, their secretory tissue is replaced by a connective tissue that is unable to synthesize hormones, and the development of follicles stops. After 10-15 years, the concentration of estrogen drops so much that it leads to a total cessation of menstruation.

Estrogens play an important biological role in ensuring adequate functioning of the mammary glands, uterus, vagina, blood vessels, skin, mucous membranes, pelvic muscles and other parts of the body.With the onset of menopause, these parts of the body are faced with a shortage of the required amount of estrogen, which can lead to various failures in these organs and tissues. The climacteric syndrome manifests itself in a variety of vegetative-neurotic disorders, osteoporosis, unwanted changes in the skin, urogenital pathologies, etc.

Symptoms

The manifestations of menopause are largely individual. They are divided into:

  • neurovegetative disorders (hot flashes, migraines, tachycardia, reduced tolerance to high temperatures, dry skin, etc.)etc.)
  • menstrual irregularities
  • psychoemotional disorders (distraction, decreased performance, obsessive thoughts, impaired appetite, decreased desire)
  • metabolic and endocrine pathologies (malfunctioning of the thyroid gland, obesity, etc.)

One of the most characteristic manifestations of the menopausal syndrome is “hot flashes” – sudden redness of the chest, facial, cervical and occipital regions, accompanied by intense sweating and a feeling of heat.The severity of the menopausal syndrome is characterized by their frequency:

  • mild form – within one dozen “tides” per day with satisfactory performance and good general condition
  • average – from one to two dozen “hot flashes” throughout the day, accompanied by a decrease in working capacity, painful sensations in the pericardial area, migraine, a significant decrease in the general condition
  • severe – over two dozen “hot flashes” a day, which, in combination with other unpleasant manifestations of menopause, lead to an almost complete loss of working capacity

Treatment

For the treatment of climacteric syndrome to be adequate, it must be preceded by a high-quality diagnostic examination.It is necessary to make a full assessment of the woman’s body, collect a personal and family history, conduct a physical examination, and also undergo some laboratory and instrumental studies. The standard set of diagnostic procedures for suspected menopausal syndrome includes:

  • Ultrasound of the reproductive system
  • analysis of the level of various hormones
  • study of uterine endometrium scraping
  • blood tests
  • mammography
  • Vaginal smear analysis

Routine examinations by a gynecologist for all women after 45 years of age also play an important role in the treatment and prevention of climacteric syndrome.This approach allows timely detection of violations in the female reproductive and endocrine systems and their correction. Treatment methods for menopausal syndrome depend on the symptoms and disorders in the body. Methods for treating this disease are divided into medication (hormonal and non-hormonal) and non-drug therapy. An integrated approach is usually practiced, including both hormonal therapy and various methods of non-drug treatment of painful conditions in menopause.

Hormone replacement therapy is the main treatment for menopausal syndrome. Hormonal drugs effectively eliminate various vasomotor manifestations of menopause, normalize the general condition of the body and well-being, improve sleep and mood, and counteract atrophic phenomena in the urogenital tract.

Hormone therapy after the onset of natural menopause is aimed at stabilizing the quality of life, maintaining the adequate functioning of organ systems.The use of hormones helps to resist various age-related metabolic disorders that often occur with menopause. The most serious of these are various malfunctions of fat metabolism, as well as osteoporosis.

Hormone replacement therapy should be based on the individual characteristics of the patient’s body and take into account the nature of her climacteric syndrome. The optimal treatment regimen is based on the selection of the dosage of drugs, the regimen of administration and the methods of administration.With menopause, even a low dose of estrogen may be sufficient, provided that the desired goals are achieved: the lipid profile improves, vasomotor manifestations stop, bone loss stops, etc.

In addition to drug therapy in counteracting climacteric syndrome, non-drug approaches are of great importance. They can greatly alleviate the condition of a woman suffering from menopausal syndrome and reduce its unpleasant manifestations.

Non-drug methods are usually based on correcting the patient’s lifestyle, improving her diet, psychohygiene and eliminating bad habits. Adherence to a healthy lifestyle is an effective method both in the treatment of climacteric syndrome and its prevention. Among the most important elements of non-drug therapy for climacteric syndrome are as follows:

  • Coping with stress with the right mindset and relaxation techniques
  • Regular moderate physical activity, such as swimming and walking
  • quitting smoking, if this bad habit is present
  • Provision of high-quality ventilation of living and working premises to avoid stuffiness
  • selection of loose clothing made from natural fabrics that provide high-quality ventilation
  • balanced and rational nutrition based on reduced consumption of meat, coffee, semi-finished products
  • inclusion in the diet of foods rich in phytoestrogens, as well as vitamin and mineral complexes, selected together with the attending physician

Many women suffering from climacteric syndrome underestimate the severity of this condition and delay contacting a specialist, which is highly undesirable.With a painful course of menopause, the help of a doctor is really necessary. It is important not to resort to self-medication and numerous dietary supplements, which supposedly effectively counteract climacteric syndrome. Such an amateurish approach can cause real harm to health in the event of an admission that is not agreed with the attending physician.

90,000 British doctors have found a way to delay menopause by 20 years

British doctors have found a way to postpone menopause by 20 years with the help of ovarian tissue transplants.This will allow not only to avoid unpleasant symptoms and dangerous diseases, but also, if desired, restore fertility.

Menopause can now be postponed by 20 years thanks to the development of British doctors, according to The Guardian . This will help to alleviate unpleasant symptoms and health problems associated with menopause.

At the age of about 50, women have menopause – a period in which menstruation stops and the possibility of conception disappears.

Menopause is the last menstrual period that occurred during the independent work of the ovaries.Natural menopause is associated with age-related depletion of the ovarian follicle storage. It usually occurs between the ages of 45 and 55. In the case of menopause before the age of 40, they talk about ovarian wasting syndrome.

During menopause, women suffer from many unpleasant symptoms.

Most of them complain of “hot flashes” – a sharp redness of the skin of the face, neck, chest, accompanied by fever and sweating. More than 20 of these seizures can occur per day. Also, many are annoyed by mood swings, migraines, problems with blood pressure, shortness of breath, nausea, tachycardia, pain when urinating.Libido disappears, itching and dryness in the vagina are tormented.

When hormonal indicators stop fluctuating, the symptoms of menopause pass, postmenopause occurs, which lasts until the end of a woman’s life. During this period, many women are faced with osteoporosis – against the background of hormonal changes there is a deficiency of calcium and vitamin D. The cardiovascular system also suffers, the risk of heart attacks, strokes, angina pectoris increases. This is due to a strong decrease in the production of estrogen in the body.

Hormone replacement therapy is used to combat the symptoms and consequences of menopause, but it is not suitable for everyone and has a number of limitations.

The procedure proposed by the ProFam specialists is quite simple – during a laparoscopic operation, the surgeon takes a small piece of ovarian tissue, which is then frozen until menopause.

When her symptoms appear, tissue can be transplanted to a well-supplied place on the body, such as the armpit, and thus estrogen levels can be restored.

A similar procedure is used for girls and women who must undergo cancer treatment – part of the ovary is removed, and after recovery is transplanted next to the fallopian tube, where the maturing eggs are then transferred.

How long menopause can be postponed depends on the patient’s age at the time of the operation. If tissue from a 25-year-old woman was used, menopause could be delayed by 20 years. 40-year-olds can only count on a five-year grace period.

“This is the world’s first project to cryopreserve ovarian tissue in healthy women solely to delay the onset of menopause,” says Yusuri Afifi, chief physician of the company.

Doctors believe that, in addition to postponing menopause, this procedure will allow the government to save significant funds by reducing the cost of treating menopause and related problems such as heart disease and osteoporosis.

“The procedure can bring significant benefits to any woman who wants to postpone menopause for any reason, or a woman who is not suitable for hormone replacement therapy,” says one of the authors of the technique, Professor Simon Fischel, an IVF specialist.

He explains that today a woman can spend 30-40 years in postmenopause, almost half her life, so she should have a way out in case of health problems.

In addition, this approach can expand the possibilities of IVF. Ovarian tissue preserved at the age of about 20 years contains many oocytes – the precursors of eggs. Their transplantation in later years may allow conceiving a child without hormonal stimulation and in vitro fertilization. A woman can use a transplant several times in her life – both to restore reproductive function, and to delay menopause.

So far, the procedure costs $ 8-13 thousand. Nine women have already frozen ovarian tissue in order to delay menopause.

This procedure, which costs between £ 7,000 and £ 11,000, is offered to women under 40 through ProFam, a Birmingham-based company founded by Simon Fishel, IVF physician and president of the UK Fertility Care Group, in collaboration with other professionals.

Richard Anderson, Associate Director of the University of Edinburgh Center for Reproductive Health, has been involved in cryopreservation of ovarian tissue for 25 years.That transplantation can restore hormone levels is “old news,” he notes, and adds, “It’s less clear how safe and effective it is.”

90,000 Climactic threat: vitamin D will reduce stress and prolong fertility | Articles

Russian doctors have created a new method for correcting the negative manifestations of menopause in women. First of all, this concerns the prevention and correction of psychoemotional disorders. Scientists have conducted animal studies that have shown that the combination of hormone therapy with individualized dosages of vitamin D3 significantly reduces depression and anxiety, as well as other negative manifestations of menopause, but this requires individually selected high doses.Also, according to indications, such therapy was carried out to a number of women with especially severe problems – it turned out that new combination therapy can prolong the period of fertility.

Not a sad age

Climax is a long period in a woman’s life associated with the gradual cessation of ovarian estrogen production and the completion of reproductive function. Its onset occurs after the age of 50. Pathological manifestations of menopause negatively affect the professional activities of women, their social activity and interpersonal relationships, which affects the quality of life.For many, menopause occurs with a whole complex of vegetative-vascular, mental and metabolic-endocrine disorders. Such problems are observed in 30-60% of women.

Scientists of the Institute of Physiology named after I.P. Pavlova RAS, with the support of the Russian Science Foundation, are developing a new method for correcting negative manifestations of menopause. First of all, this concerns the prevention and correction of psychoemotional disorders. As the leading researcher of the Laboratory of Neuroendocrinology of the Institute of Physiology named after I.I.P. Pavlova Julia Fedotova, during the research, scientists have established a relationship between low levels of vitamin D3 (cholecalciferol) in the body and a predisposition to the onset and development of affective disorders in women during menopause.

Photo: Global Look Press / imago-images / Julia Pfeifer

– Studies have shown that the level of vitamin D3 in women may be one of the predictors of the development of anxiety-depressive disorders during the initial stage of menopause.At the same time, the prevention of a deficiency of this substance can play a leading role in preventing the development of psychopathologies, the specialist explained.

From 2016 to 2018, scientists performed two parts of the study: preclinical (in animals) and clinical (in volunteers). Now the work continues.

Case in the dose

Previously, all doses and treatment methods were worked out on rats . The experiment involved females of different ages: young (2.5–3 months), middle-aged (12–14 months) and old (16–18 months).They recreated an experimental model of menopause: the animals had their ovaries removed, and then they waited three months for hormone levels to roughly match those of menopause in women. Then, all three groups of rats of different age were injected with vitamin D3 in three different doses: low, medium and high. The vitamin was administered alone or in combination with a low dose of the hormone estradiol (similar to hormone therapy in women).

In some cases it was possible to achieve a strong antidepressant effect, and in some it did not work at all.That is, it turned out that therapy with vitamin D3 is effective only in the case of an individual approach, taking into account age and hormonal status.

Photo: TASS / Petr Kovalev

Then, scientists conducted clinical trials on women of different ages, including those who had menopause ahead of schedule (33 years). Clinical studies have confirmed the effectiveness of the combined use of hormone therapy in combination with vitamin D3 in different doses, depending on the age of the patients.

In parallel, we found that the appointment of vitamin D3 helps restore hormonal levels in young women with premature menopause, thereby increasing the likelihood of conceiving a child in conditions of depleted ovaries , – noted Yulia Fedotova. – It can be used in preparation for in vitro fertilization.

Reception under supervision

Scientists have prescribed an algorithm for choosing drug doses and treatment tactics for different age groups.The authors of the work emphasize that the main thing in such therapy is compliance with dosages depending on the woman’s age and her hormonal background.

Director of the Institute of Biology and Biomedicine at Lobachevsky University Maria Vedunova told Izvestia that the role of vitamin D in the functioning of the body, especially the female, both in the reproductive and age aspects, is extremely difficult to overestimate.

– Vitamin D is a necessary participant in the synthesis of female hormones, especially estrogens. For a long time in clinical practice, there have been approaches that actively use vitamin D to correct hormonal and age-related changes in the female body. This therapy was not always effective, most likely, this was due to the difficulty of controlling the absorption of vitamin , she said.

Photo: TASS / YAY

Vadim Tseilikman, director of the Higher Medical and Biological School of SUSU (a university that participates in the 5-100 project), is confident that the proposed therapy can be effective.

Undoubtedly, Professor Fedotova’s research deserves attention and support. At present, the attention of researchers from different countries is drawn to vitamin D as a promising antidepressant . Its biological effect is not limited to bone tissue, he said. – In many internal organs there are receptors for the vitamin, and its biological action is similar to that of hormones. These properties served as the basis for studies of its effect on behavioral activity.

Previously, scientists from the United States conducted a major study in which they showed that daily intake of 400 IU of vitamin D (as recommended by the US Institute of Medicine) in combination with 1 mg of calcium does not reduce the risk of depression. At the same time, the authors note that in order to determine whether the vitamin may be useful in prevention and treatment in specific populations, more studies are required using higher doses. This has been done by Russian scientists who have confirmed that much higher dosages are required for postmenopausal women.However, the vitamin should be used under the supervision of the attending physician, and in case of normalization of its level, a break should be taken between courses to avoid an overdose.

READ ALSO

Is there sex after menopause and 7 more frank questions to the gynecologist | HEALTH

And there are many questions that did not torment our grandmothers, because the lifestyle, priorities and possibilities of medicine were completely different. Do I need to protect myself during menopause? When is it not too late to have children? Are expensive drugs that doctors prescribe right and left so necessary and safe?…

The Ural experts answered the most popular questions of our readers: Elena Piskunova, Ph.D., obstetrician-gynecologist, head of the department of gynecology of the Center for Cosmetology and Plastic Surgery named after S.V. Nudelmana, a member of the European Association of Urogynecologists (IUGA), the Russian Association of Gynecologists-Endoscopists, the American Association of Gynecologists-Endoscopists (AAGL), and Yulia Pertsova , obstetrician-gynecologist, gynecologist-endocrinologist, ultrasound diagnostics doctor at the Olmed Medical Center Russian Association of Specialists in Aesthetic Gynecology.

Let’s cancel the climax?

– Modern medicine works miracles. Is it possible to completely cancel menopause?

Elena Piskunova: – The climacteric period is one of the normal periods in a woman’s life, everyone experiences it. But at the same time, you can live a full, high-quality life without losing your ability to work and interest in life.

This is the transition period between regular menstruation and confident menopause (the year when regular menstruation is absent).Concomitant signs: increased fatigue, hot flashes, night sweats, intermittent sleep, loss of interest in life – the desire to “lie on the couch.” Possible urogenital disorders (cystitis, dry mucous membranes, decreased sexual desire), changes in the quality and condition of the skin, hair, nails, etc. These external manifestations are a signal that the body has not learned to live in conditions of hormone deficiency and to accurately dose the decreased amount of estrogen for vital functions. This condition must pass.

In conditions of estrogen deficiency, internal changes occur, such as loss of calcium in the bones and the development of osteoporosis, changes in insulin levels and weight gain, increased blood pressure, impairment of memory, concentration, attention, and eye problems. Age-related changes cannot be reversed, but they can be postponed for a sufficiently long period. In order to feel good and not to lose the quality of life, one must visit a doctor – first of all, not with illnesses, but for a preventive purpose, in order to discuss their age characteristics and form an individual algorithm of behavior for a certain period of life.

Julia Pertsova: – On average, menopause occurs at about 50 years old, but this time can vary greatly. Some women tolerate it very hard, with impaired blood pressure, nervous disorders and other changes. To neutralize the manifestations of the menopause and help the body cope with hormonal changes, a healthy lifestyle is important: proper food, diet, it is important to reduce stress levels, bad habits and destructive behavior. Sleep should be 8 hours, and you need to fall asleep before 23 hours.Water procedures and hardening have a very beneficial effect on the nervous system. Physical activity is required, at least 40 minutes a day of walking.

The basis of a healthy diet is plant food, it contains substances with antioxidant and anti-inflammatory properties that prevent blood clots, regulate blood pressure, enzyme activity, normalize blood glucose levels, correct the lipid profile and myocardial state.

Are special drugs for menopause a risk factor for oncology? Why are they assigned to everyone in a row?

Yu.Pertsova: – Now there are no hormones that we divide into male and female. All sex hormones – estrogen, progesterone, and even testosterone – are equally needed by both men and women. Each hormone has its own role. A woman first encounters sex hormones during puberty, and then blooms and lives throughout her life until the onset of menopause. In the climacteric period, everything that determined the state of health and well-being disappears along with the cessation of the production of sex hormones.The external reflection of menopause very quickly affects the skin, because it is she who loses collagen, which is responsible for turgor. In the first two years of menopause, a loss of 30% of collagen occurs.

Substitution drugs neutralize all undesirable manifestations of hormone deficiency and add to youth, pushing back and preventing age-related diseases. For a full examination and identification of the risks of side effects and contraindications when prescribing hormone replacement therapy for a woman after 45 years of age or at the first manifestations of menopausal disorders, it is imperative to visit a doctor.

E. Piskunova: – We cannot say that specialized drugs are vital. But we unequivocally vote that they can and should be applied. There is a big misconception that only in Russia do doctors offer specialized drugs to relieve the symptoms of menopause, in fact, they are widely used all over the world. We offer a standard approach that is no different from the European one.

Before you start taking any hormonal drugs, a comprehensive examination is mandatory.The task of the doctor is, first of all, to exclude life-threatening conditions: the presence of strokes, thrombosis, ulcerative processes, autoimmune diseases, oncology, pronounced stages of varicose veins, etc. With caution, drugs are prescribed for peptic ulcer disease, high blood pressure or an increase in triglycerides.

The doctor selects the drugs individually, and they do not cause cancer by themselves. If oncology occurs, then it happens in the presence of drugs, but not as a result.If you fulfill all the appointments, come to control visits and consult a doctor with any changes in your well-being, the drugs have only a positive effect. As a result, even this period of her life, a woman can live qualitatively, fully and with dignity.

Features of sex with menopause

What are the differences in female sexuality during menopause, should I use contraception?

Y. Pertsova: – With age, the level of estrogen decreases more than the level of testosterone.Namely, testosterone is responsible for sexual activity. And it turns out that testosterone does not disappear anywhere and does not fall. So the desire doesn’t go away. Women’s physiology is such that it is after menopause that you sometimes want more sex. A modern woman who has entered the climacteric period no longer has a bunch of somatic diseases, like our grandmothers, and can live a full sexual life without thinking about the possibility of getting pregnant.

If the cycle still comes, albeit irregularly, it is better to protect yourself, since single ovulations are possible and there are risks of unwanted pregnancy.In this case, it is better to visit a gynecologist and, together with a doctor, choose the most appropriate method of contraception, taking into account all the health features of a particular woman. Physiological inconveniences will help to overcome modern pharmacological agents, such as lubricating gels.

Late pregnancy: trends and risks

In the West, pregnancy has become a trend after 30 or even 40 years. What do our doctors think about this?

Y. Pertsova: – Indeed, recently more and more famous personalities are choosing pregnancy at an older age.The duration of an active life of the population is rapidly increasing due to the achievements of modern medicine, in addition, many want to first become financially independent, to realize themselves in a career.

There are certain advantages of pregnancy after 40 years: a long-awaited late child is a great joy, it brings a lot of positive emotions and prolongs the life of the parents. According to some scientific studies, late children are smart and talented. Mature parents are calmer, wiser and more conscientious.They are the best educators, make mistakes less often and treat children more carefully. As a rule, at the age of 40, the financial situation of the parents is better than at the age of 20. The energies of your life are renewed, together with the baby a lot of new and interesting things come into your life.

But there are many disadvantages of being born after 40: the likelihood of infertility is greater and the risk of miscarriage is higher. It is more likely that a woman will have to resort to high reproductive technologies or receive special medical support.The likelihood of having a baby with serious congenital diseases increases.

E. Piskunova: – We cannot present medical indications like “at 40 it’s too late to carry a pregnancy” or “at 40 you cannot have your first child”. The first pregnancy at forty in Russia is not yet a very common fact, but, nevertheless, it takes place. The doctor, in my opinion, can only place some medical accents when carrying a pregnancy is clearly contraindicated or there are confirmed individual risks.And at what period of her life a woman has decided for herself that it is important for her, that she wants it – we always leave this decision to her.

Getting pregnant after thirty-seven is somewhat more difficult than at a younger age. After thirty-seven years, the number of ovulatory cycles drops sharply, this is statistically calculated: ovulation occurs every three to four months. This is at its best, ideally. There will be more risk. And this means that the woman will be examined more thoroughly.

In particular, a special analysis for the risk of genetic mutations is usually recommended.If during the first screening ultrasound (at 12-13 weeks) possible malformations are identified, there is still an opportunity to terminate the pregnancy. The next screening period will be at 18–20 weeks, during this period any inferiority in the development of the fetus must be clearly identified, and the woman still has the opportunity to terminate the pregnancy. After 22 weeks, this is already prohibited by law and everything is done to preserve the fetus, if necessary, intrauterine operations are performed.

Do you trust advertising?

Why do you need panty liners?

E.Piskunova: – A healthy woman does not need a daily sanitary napkin. Her linen remains clean, normally there should be no smell or discharge. If there is a smell, you do not need to buy a pad, but go to the doctor. And in general, the use of all these lactacids, epigen-sprays – yes, it does not harm health, but they are unnecessary for a healthy woman. If you cannot do without additional funds, you should go to the doctor and solve your health problem.

How to choose a gynecologist?

E.Piskunova: – It is advisable that one doctor observe you throughout your life – you get used to the doctor, and he knows your characteristics and is able to build a coherent monitoring system for you. Therefore, patients usually follow the doctor from clinic to clinic. And it is not so important whether you are being observed in a paid clinic or in a free one, the head and hands of a professional are important.

If for some reason you are faced with the need to change a doctor or a hospital, it is certainly very important to pay attention to the availability of certificates.In addition, your doctor should be versatile, have knowledge of both endocrinology and the treatment of inflammatory diseases; and if he is also an operating practitioner, that’s just great.

It is equally important how the reception is arranged: the confidentiality of the environment provides the necessary condition for confidentiality. If the doctor is a man, it is very important that a nurse is present at the appointment.

Why visit a gynecologist regularly if nothing bothers you?

Yu.Pertsova : – The absence of complaints does not mean complete health. Even if you feel good, you cannot be sure that you are completely healthy. Routine examinations and screening studies contribute to the early diagnosis of oncopathology and a number of gynecological diseases, which can save not only life, but also reproductive function. Every year, every woman should visit a gynecologist with a diagnosis (examination by a doctor with anamnesis, bimanual palpation and examination of the mammary glands, taking a smear for oncocytology, as well as colposcopy and ultrasound diagnostics, if indicated).

Some symptoms should be alerted to visit a doctor unscheduled: pain in the lower abdomen, the appearance of bloody discharge outside the menstrual cycle, in the postmenopausal period and after sexual activity. The appearance of odorless discharge, itching, burning, yellowish, greenish discharge, menstrual irregularities. Other issues that require a visit to the doctor: selection of contraception, frequent change of sexual partners, non-pregnancy during the year.

Menopause (hormonal profile)

Comprehensive blood test designed to examine a woman at the onset of menopause.

Synonyms Russian

Blood tests during menopause.

Synonyms English

Lab Diagnosis of Menopause.

What kind of biomaterial can be used for research?

Venous blood.

How to properly prepare for the study?

  • Eliminate fatty foods from the diet within 24 hours before the study.
  • Do not eat for 8 hours before the study, you can drink clean non-carbonated water.
  • Completely exclude (in agreement with the doctor) taking medications within 24 hours before the study.
  • Eliminate physical and emotional stress for 24 hours before the study.
  • No smoking within 3 hours prior to examination.

General information about the study

Menopause is the termination of the cyclic hormonal activity of the female body and menstruation. This is a natural outcome of the decline in female reproductive function with aging.The timing of menopause depends on many factors, including genetic factors and a woman’s overall health. The average age at menopause is 51 years.

Usually menopause is preceded by a period of irregularities in the menstrual cycle (lengthening of the cycle, skipping a cycle, irregular menstruation), called premenopause. Menopause is considered to have occurred if there has been a persistent absence of menstruation for more than 12 months.

Menopause is accompanied by irreversible hormonal changes in a woman’s body – a decrease in the level of female sex hormones (estradiol) and an increase in the level of hormones in the anterior pituitary gland (luteinizing hormone, LH, and follicle-stimulating hormone, FSH).

Estradiol is the main sex hormone in women of reproductive age. It is produced by the ovaries. Its main function is to prepare the endometrium of the uterus for embryo implantation. Also, estradiol has a suppressive effect on the production of FSH and an activating effect on the synthesis of LH. The concentration of estradiol increases in the first half of the menstrual cycle and reaches its maximum during ovulation. Violation of the production of estradiol by the ovaries leads to anovulatory cycles and NMC and, as a result, to the complete cessation of menstruation.

The changes in FSH and LH observed during menopause occur in response to a decrease in estradiol levels. FSH during menopause is usually increased more significantly than LH. The FSH level is considered elevated if its concentration is two or more times the average FSH concentration of a woman of reproductive age, measured in the early follicular phase (more than 30 IU / L).

Menopause is generally a clinical diagnosis. In some cases, however, a laboratory examination is required. It is especially indicated for women with signs of menopause at a younger age.The onset of menopause before the age of 40 is called premature ovarian failure (formerly called early menopause). It is characterized by a decrease in estradiol and an increase in LH and FSH. The causes of this disease are not fully understood, but it is believed that the autoimmune process and infections (herpes virus, CMV) are important. Premature ovarian failure occurs as a result of exposure of the ovaries to ionizing radiation (radiation therapy), chemotherapy, or surgical removal of both ovaries.Inhibin B and anti-Müllerian hormone testing may also be recommended to obtain complete information on ovarian function if premature failure is suspected. It should be noted that premature ovarian failure is not the most common reason for a young woman to have no periods. Additional research is done to rule out other diseases and conditions (such as pregnancy).

Symptoms typical for the onset of menopause (night sweats, hot flashes, menstrual irregularities) can also occur with hyperthyroidism.Therefore, when examining a woman with such complaints, it is advisable to assess the function of the thyroid gland using thyroid-stimulating hormone (TSH) and thyroxine (T4). It is optimal to measure free, and not total thyroxine, since it is free thyroxine that has effects on organs and tissues. Hyperthyroidism can be attributed to a variety of medical conditions. In most cases, it is caused by Graves’ disease, in which there is an increase in the concentration of free T4 and a decrease in TSH. An increase in TSH concentration and a decrease in T4 levels will, on the contrary, indicate that the cause of hyperthyroidism is a pituitary adenoma.

Given that menopause is associated with the progression of certain diseases (osteoporosis, cardiovascular disease, dyslipidemia), when examining a woman with menopause, additional laboratory tests may be required, including markers of bone tissue remodeling, lipid profile and, when planning hormone replacement therapy, a complete blood count and liver and kidney function.

What is the research used for?

  • For laboratory diagnosis of menopause;
  • to exclude hyperthyroidism in a woman with signs of menopause.

When is the study scheduled?

  • For menopausal symptoms: persistent absence of menses for more than 12 months, hot flashes, night sweats, anxiety and mood changes.

What do the results mean?

Reference values ​​

Change in the concentration of hormones characteristic of menopause :

90,000 Depression in Menopause – Symptoms and Treatment Methods

Climax is a scary word for any woman.It is characterized by oppression of the reproductive system due to the onset of a certain age (50 years and above). Menstruation often stops or is extremely irregular.

For a woman, menopause is a new stage in life, a kind of test. For some, it goes away quickly and painlessly, for others – with psychological and physical problems.

On the part of the nervous system, it can be depression, irritation, tearfulness, mood swings (just a minute ago I wanted to laugh, but now I want to cry).

The appearance changes markedly: the skin fades, loses its elasticity, a wrinkled “mesh” appears on the face, and the hair is actively falling out. Health problems may also occur:

  • regular tides;
  • 90,021 insomnia;

    90,021 pressure surges;

    90,021 dizziness;

  • nausea;
  • decreased libido;
  • 90,021 obesity;

  • osteoporosis, etc.

Naturally, not always a woman can put up with herself, a new one.Against this background, climacteric depression develops in women, which requires very serious treatment.

Reasons for the development of depression

Let’s dwell on why women develop a similar condition during menopause:

  1. Hormonal changes lead to fluctuations in estrogen levels throughout the day. Hence the “frantic” mood swings. The production of serotonin, which is responsible for well-being, drops sharply.
  2. Psychological discomfort associated with the rejection of negative changes in appearance and the approach of such a frightening old age.
  3. Menopause is accompanied by unpleasant symptoms that also spoil the mood: sweating and frequent urge to go to the toilet.

Symptoms

It is important to understand that depression with menopause requires treatment, because life can become simply unbearable. The main thing is to consider dangerous symptoms in time.

  • A sharp decline in strength – you do not have any vital resources, even if you have a good sleep.
  • Fear of communication develops – any contact becomes a burden, there is no desire to communicate with family, relatives, especially with friends and colleagues.
  • Self-esteem is colossally reduced for obvious reasons, hence an even greater desire for solitude and voluntary isolation.
  • Permanent pessimism, lack of joy from delicious food, a good movie, a new purchase.
  • Hot temper and irritability

Treatment

Treatment of depression in women is, of course, necessary. After all, life does not end during menopause. It can also be full of vibrant colors, scents and events.

To deal with the problem, you need to contact several specialists:

  • The therapist conducts the initial examination, gives directions for tests and examinations.
  • An endocrinologist, having studied the test results, will conclude about the woman’s hormonal background. He will prescribe hormones if necessary. The therapy involves the use of a synthetic hormone. After taking it regularly, women notice positive changes in their condition
  • A cardiologist will be able to rule out the presence of a disease of the cardiovascular system.
  • The neurologist will find the causes of irritation, mood swings and also rule out certain diseases of the nervous system that may have similar symptoms.

It is very important to understand that under certain manifestations of menopause, more serious diseases are not masked. If the examination showed that there are no illnesses, you can start “eliminating” these symptoms and treating climacteric depression.

Here such a specialist as a psychotherapist comes to the fore.Menopausal depression in women includes the following treatment: drug therapy and psychotherapy sessions.

As for drugs, here we can talk about antidepressants of the SSRI group. They are good because they have a minimum number of side effects, act quite quickly and are easily tolerated by the body.

Preventive measures

The onset of menopause is inevitable. But a woman can always “spread” straws for herself in advance so that menopause would be as comfortable as possible.How can this be done?

  1. Start taking non-hormonal herbal preparations that are as harmless to the body as possible.
  2. Massage, pine baths and yoga very well relaxes and relieves insomnia.

It is important for women to understand that depressive moods during menopause are not the norm. They should not be, in no case should you put up with them. A woman has the right to enjoy life at any age.

It is important to start the steps towards happiness.It is very difficult to make them yourself. It is important that a reliable specialist, a doctor who knows his business, is walking nearby!

But at the same time, do not forget that you can help yourself a little:

  • Try to go out to people. If you find it very difficult to communicate with people, do not do it. But it is important to be among people, to walk more.
  • Pay attention to your appearance. Yes, there are problems with the skin, but now there are many cosmetic products and procedures that will help to significantly improve the appearance, make wrinkles shallow and invisible.Don’t forget about decorative cosmetics and pleasant shopping. Even a small wardrobe update will be a lot of fun.
  • Find a new hobby. An interesting activity can brighten your days and speed up your exit from depression. Hobbies can be related to handicrafts, dancing, cooking. It all depends on your personal interests.

Do not treat menopause as a tragedy, otherwise your climacteric depression will only worsen. Realize that this is a temporary stage in your life that you will surely go through successfully.Take it as positively as possible. You will see that after a while, the depression will begin to subside, and over time you will forget about it.

90,000 Menopause in women – symptoms and treatment, HRT with menopause during menopause

Menopause is a natural physiological process in a woman’s life, the basis of which is hormonal changes in the body. It occurs when the ovaries stop producing female sex hormones – estrogens and progestins, which leads to decreased fertility.

This happens about two years after the last menstrual period. The body begins to gradually fade away, the follicular supply and the amount of estrogen decrease.

Menopause, or menopause, is a whole period in a woman’s life, which, on average, begins after 45 years. Nature is so conceived that up to a certain point a woman has hormonal reserves, and then they are gradually depleted.

The first sign is menstrual irregularities, called perimenopause, and can last up to several years.Then menopause sets in. This period is accompanied by various symptoms and unpleasant sensations that can be corrected by contacting a competent doctor, preferably a gynecologist-endocrinologist.

Sign up

Menopause symptoms

Symptoms of menopause make themselves felt when there is a deficiency of sex hormones – estrogens and progestins. The very first symptoms that speak of hormonal changes in a woman’s body:

  • Tides.The work of norepinephrine and dopamine (hormones involved in thermoregulation) is disrupted. Hot flashes are sudden and unpleasant hot flashes. They can last from a few seconds to several minutes. About 70% of women are affected by them.

  • The menstrual cycle is shortened;

  • Unmotivated mood change;

  • Dry vaginal mucosa;

  • Anxiety, insomnia;

  • Lack of sex drive;

  • Depression;

  • Increased blood pressure;

  • Decreases skin elasticity;

  • The body weight increases.

For some reason, hormone levels may decrease faster in women.

Factors that bring menopause closer:

  1. Stress. It is accompanied by a powerful release of cortisol (adrenal hormone), which performs various functions to mobilize the body as a whole. When stress occurs, the body does not care what kind of events provoked it: a quarrel with a friend, a dog bite, or you did not find a suitable dress for your birthday.If in response to them you behave emotionally, then your hormonal reserves are mobilized. If this stress is regular, then the body produces less and less sex hormones. And then menstrual function, the ability to conceive and bear children suffers. If it is impossible to get out of constant stress on your own, you need to contact a specialist.

  2. Sleep and rest. When we have a lack of sleep, it also negatively affects the production of sex hormones. Even when they come home, many women do not give themselves time to rest. Very often, a woman misses this important period when sex hormones have to be restored (from 22:00).But it is in a dream that the most important hormones are produced, including melatonin, follicle-stimulating (FSH) and luteinizing (LH) hormones, which greatly affect the state of the body in general and the female reproductive system in particular. Therefore, it is important to go to bed before 22-23 hours. It is also important not to look at your phone or laptop before bed, so as not to irritate the cerebral cortex and not load your head with unnecessary information.

  3. Job. It doesn’t have to be physically exhausting or stressful.In this case, you can keep your sex hormones as long as possible. But the paradox is that if a woman is responsible and purposeful, then even minimal stress cannot be avoided. In this case, you need to return to the first point and adjust the state of affairs, as well as learn to manage your emotions. Also, during the day, you need to eat a balanced diet. Nutrients such as protein and fat are involved in building sex hormones. In addition, if you have a sedentary job, it is necessary to periodically get up, walk and do simple exercises to improve the flow of blood in the pelvis.This will nourish the gonads and ovaries.

  4. Deficiencies of trace elements, vitamins, nutrients. A woman can “lose” them due to stress, improper lifestyle, or because they are poorly absorbed in the intestines. If it is chronically inflamed, and in the diet there is an excess of junk food, sweet and fried, then the nutrients will be poorly absorbed by the intestines. Also, a woman does not receive the necessary trace elements if she does not eat enough fish and meat, that is, protein foods.Often doctors, if it is impossible to quickly fill the deficiencies of useful elements, prescribe dietary supplements (biologically active additives) to a woman or, in more complex cases, prescribe intravenous therapy.

  5. Intoxication (smoking, alcohol, dirty air). They block those receptors that must be sensitive to minerals and trace elements. In this case, nutritional deficiencies are almost inevitable.

call me back

Diagnostics and treatment of menopause in Expert Clinics

The doctors of the Expert Clinics have extensive experience in managing women with menopause and in restoring their hormonal balance.The medical staff of the clinic includes gynecologists and endocrinologists with fundamental knowledge in the field of integrative anti-aging medicine, which allows them to work with each patient as delicately and efficiently as possible.

Our doctors also effectively solve the problem of early menopause, returning women to well-being and the opportunity to experience the joy of motherhood.

Patient management looks like this:

  1. Consultation with a gynecologist-endocrinologist.It will help identify risk factors that can accelerate the loss of female sex hormones.

  2. Ultrasound of the pelvic organs. The study will determine the structure of the uterus, appendages, ovaries. If the supply of follicles has decreased, we can talk about the approach of menopause.

  3. Blood test, including hormones. Which ones, the doctor determines, depending on the history and complaints of the patient.

  4. Hormone replacement therapy (HRT).To alleviate the symptoms of menopausal syndrome, you need to tidy up the production of a female hormone – estrogen. This can be helped by hormones, which are introduced from the outside in the form of gels, suppositories, tablets. They contain the same sex hormones that a woman produces during her period. Hormone therapy should only be prescribed by a physician on a purely individual basis. Note that the doctors of Expert Clinics try to select the minimum dosage of hormonal drugs, which in each specific case should work 100% and without risks.

  5. Herbal therapy. This is an alternative method of HRT, which involves the use of preparations containing phytoestrogens developed from plants, rather than chemicals. They are created for women who have contraindications to the use of synthetic drugs. For example, they may contain extracts of clover, conifers and soybeans.

Thanks to a personalized approach, experienced doctors at Expert Clinics restore a second youthfulness to ladies, excellent well-being and a radiant appearance.

Methods for relieving climacteric symptoms

Menopause not only entails unpleasant symptoms like hot flashes and increased irritability, but also makes a woman more vulnerable to various diseases. So, due to hormonal changes during menopause, bones become more fragile, which is fraught with osteoporosis and frequent fractures. Also, women have a high risk of developing diabetes mellitus and cardiovascular diseases.

Therefore, it is so important not only to see a doctor at the first signs of menopause, but also to adjust your habits.For example:

  1. Adjust sleep patterns. Women who have hot flashes, sweating, severe fatigue should definitely pay attention to their lifestyle. And, most importantly, they need to go to bed on time (at 22-23 hours). It is advisable to ventilate the room in advance, and the last meal should be no later than 3 hours.

  2. Reduce the amount of easily digestible carbohydrates in the diet. We are talking primarily about bakery products, as well as products containing sugar.The fact is that with age, they are absorbed less and less, and body weight begins to grow. You should also avoid fatty, fried, smoked foods. They can aggravate the manifestations of sweating, hot flashes, and so on.

  3. Physical activity. Even small but regular exercise can reduce sweating and hot flashes. Plus, exercise is great for strengthening bones, which become more fragile over time.

A careful and attentive attitude to themselves and their health will help ladies to maintain femininity and self-confidence for many years.

Sign up for a consultation

.