Age at Menarche and Menopause, Reproductive Lifespan, and Risk of Cardiovascular Events Among Chinese Postmenopausal Women: Results From a Large National Representative Cohort Study

Abstract

Background:

At present, the association between age at menarche and menopause, reproductive lifespan, and cardiovascular disease (CVD) risk among Chinese postmenopausal women is not clear, and some related researches are contradictory.

Methods:

A total of 6,198 Chinese postmenopausal women with a mean age of 63.6 years were enrolled at baseline in 2012–2015 and followed up for 5 years. A standardized questionnaire was used to collect relevant information by well-trained interviewers. Physical examination of the participants was performed by trained medical staff. CVD events were observed during follow-up. Cox proportional hazards models were used to estimate hazard ratios between reproductive characteristics and CVD events.

Results:

Age at menarche was positively associated with CVD events (HR, 1.106; 95%CI, 1.047–1.167). There was a negative association between age at menopause and CVD risk in postmenopausal women with comorbidity (HR, 0.952; 95%CI, 0.909–0.996). Reproductive lifespan was negatively associated with CVD events (HR, 0.938; 95%CI, 0.880–0.999). The CVD risk increased by 10.6% for every 1-year increase in age at menarche. The CVD risk reduced by 6.2% for every 1-year increase in age at menopause in women with comorbidity. The CVD risk reduced by 3.8% for every 1-year increase in reproductive lifespan.

Conclusions:

Based on the large prospective study with a nationally representative sample, Chinese postmenopausal women with late age at menarche and shorter reproductive lifespan have higher risk of CVD events.

Introduction

Cardiovascular disease (CVD) is the dominant cause of death throughout the world (1), accounting for 32% of the total deaths (2). In China, CVD is the leading cause of death and disability (1), accounting for approximately 45% of all deaths (3). Meanwhile, CVD as the principle cause of death in women is still under-recognized and undertreated (4). Therefore, comprehensive recognition of CVD risk factors and timely implementation of appropriate interventions for women is of tremendous public health importance.

Menarche is a marker of puberty and the onset of ovarian and other endocrine functions relating to reproduction (5). The results of previous studies on the relationship between age at menarche, menopause, reproductive lifespan, and the risk of CVD are inconsistent (6–11). For example, a systematic review revealed that three out of four studies show a generally linear association between a decrease in age at menarche with an increase in CVD risk (11). However, the UK Million Women Study manifested a significant U-shaped relationship between age at menarche and coronary heart disease (CHD) risk (6). Data from Asian populations were also contradictory and inconclusive (11).

Age at onset of menopause may be a marker for not only reproductive aging but also for general health and somatic aging (12). Adverse changes in CVD risk factors occur around the menopausal transition (13–15). A meta-analysis including 50,000 Western women showed a negative linear association between age at menopause and CVD (16). A follow-up study found a non-significant increased risk of death caused by CHD and stroke among women with earlier natural menopause (12). This discrepancy may be due in part to a variety of confounding variables including genetic background, race, study design, or environmental factors amongst different populations.

The interval between menarche and menopause defines a woman’s natural reproductive span. Due to exposure to different hormonal levels, early or late onset of these events may be associated with increased risk of many chronic health problems. However, the association between duration of reproductive lifespan and CVD risk has not been investigated thoroughly. A shorter duration of reproductive life span was associated with a higher Framingham Risk Score. However, this study was limited by its cross-sectional design to investigate a long-term CVD event risk (17). Results from the Australian Longitudinal Study of Women’s Health showed that an increase in reproductive lifespan per year was associated with a 7% reduction in stroke risk, but this association disappeared when only the duration of endogenous estrogen exposure was considered (18). Further, the association was either null or mixed (19, 20). These findings suggest that the association between reproductive lifespan and CVD is not completely clear and requires further investigation.

Most previous studies addressing this objective are conducted in Western populations. Asian women, including Chinese women, have different menstrual and reproductive patterns as well as different lifestyle factors compared with women living in Western countries. At present, there is a lack of clear and comprehensive researches on the relationship between age at menarche, menopause, reproductive lifespan, and CVD risk in Chinese women. Based on a national representative cohort study, we investigate the associations between age at menarche and menopause, reproductive lifespan, and the CVD risk and examine the relationship in subgroups amongst Chinese postmenopausal women.

Materials and Methods

Study Design and Participants

The Study on Prevalence and Key Technologies of Important Cardiovascular Diseases in China conducted from October 2012 to December 2015 was a large-scale representative CVD cross-sectional survey in China. A stratified multistage random sampling method was used to select about 500,000 nationally representative subjects aged ≥15 years from 262 districts and counties in 31 provinces of mainland China to investigate demographic characteristics, lifestyle risk factors, pharmacological treatment, female reproductive related characteristics and so on. In addition, the second sampling was carried out on the project. The selected districts/counties were divided into eastern, central and western region, and then stratified by urban and rural areas, 16 cities and 17 counties were selected by simple random sampling method. Random sampling was carried out in the above 33 districts/counties by stages. In the last stage, only respondents aged 35 and above were randomly selected from eligible regions to obtain blood samples for investigation of fasting plasma glucose (FPG), total cholesterol (TC), triglycerides (TG), low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C) levels. Finally, those 30,036 individuals who completed the baseline survey were followed up in 2018–2019. 5,361 people lost to follow-up within the 5 years and the overall rate of follow-up was 82.15%. A total of 6,198 postmenopausal women were included in the final analysis after exclusions of 916 people with history of CVD, 11,106 male participants, 5,379 non-menopausal women and 1,076 postmenopausal women with incomplete information or errors (Figure 1).

FIGURE 1

The written informed consent was obtained from each participant. The Ethics Committee of Fuwai Hospital (Beijing, China) approved this study.

Baseline Measurement and Data Collection

A standardized questionnaire was used to collect information on demographic characteristics, lifestyle risk factors, medical history, and characteristics related to female reproduction by well-trained interviewers in 2012–2015. Height and weight were measured using a standardized cartesian and an OMRON body fat and weight meter (V-body HBF-371, Omron, Japan) with participants wearing thin clothing and no shoes. Blood pressure of the participant was measured using an Omron HBP-1300 professional portable sphygmomanometer (Omron, Kyoto, Japan) on the right arm in the sitting position after resting for at least 5 min. Laboratory examinations were performed on venous blood samples collected after at least 8 h of fasting at night. FPG, TC, TG, LDL-C, and HDL-C levels were measured by a central core laboratory (Beijing Adicon Clinical Labora-tories, Inc., Beijing, China).

Follow-Up and Outcome Measures

During 2018–2019, we tracked CVD events via interviewing participants or their proxies in-person or via telephone or mail questionnaires, and further examined medical records for reconfirmation. Participants’ CVD events were initially recorded by local investigators, and then hospital records were reviewed by the central adjudication committee of Fuwai Hospital (Beijing, China) to determine the final diagnosis. CVD events were defined as CHD, stroke, chronic heart failure, and death due to CVD. The criteria for stroke included non-fatal and fatal stroke (subarachnoid hemorrhage, ischemic stroke, intracerebral hemorrhage, and unspecified stroke). CHD was defined as non-fatal (including myocardial infarction, coronary artery bypass graft surgery, or percutaneous coronary intervention) and fatal CHD (such as fatal myocardial infarction and other coronary deaths).

Variable Definition

At baseline, each participant was asked her age at the time of her first period, which was recorded as age at menarche. Menopausal status was defined based on the World Health Organization’s definition of menopause as the absence of menstruation for ≥12 months, and the age at which menopause occurred was recorded at baseline. The reproductive lifespan was defined as the interval between age at menarche and menopause.

Body mass index (BMI) was calculated by dividing weight (kg) by height squared (m²). Criteria for overweight and obese were defined as BMI between 24.0 and 27.9 kg/m² and BMI ≥ 28.0 kg/m², respectively (21). Alcohol drinking was defined as consuming an alcoholic beverage at least once per week in the past month. Smoking was defined as people who have smoked at least 20 packets of cigarettes in their lifetime and were still smoking (22). Diabetes was defined as fasting blood glucose ≥7 mmol/dL or was diagnosed with diabetes by a doctor or was prescribed hypoglycemic drugs within 2 weeks (23). According to the Guidelines for Dyslipidemia in China, TG ≥ 2.26mmol/L or TC ≥ 6.22mmol/L or HDL-C < 1.04 mmol/L or LDL-C ≥ 4.14 mmol/L or prior lipid-lowering medication or prior diagnosis of dyslipidemia (24). Have pharmacological treatment is defined as taking any one of anti-hypertensive, hypoglycemic, or anti-hyperlipidemia drugs. Comorbidity refers to any combination of two or more of three diseases: diabetes, hypertension and hypercholesterolemia following previous study (25). Parity was defined as the number of live babies a woman gives birth to, whether or not the baby dies after delivery (26).

Statistical Analysis

Baseline characteristics of participants were presented as mean and standard deviation (SD) for normally distributed data or as a proportion for categorical data. The t-test, χ² test, and variance analysis were used to compare variables between the different groups. Logistic linear regression model was used to explore the trend of variables. Multivariable Cox proportional hazard model was used to estimate Hazard ratios (HRs) and 95% confidence intervals (CIs) for CVD events associated with age at menarche (classified as ≤13, 14, 15, 16, and ≥17 years) with 15 years as the reference group, age at menopause (classified as ≤44, 45–46, 47–48, 49–50, and ≥51 years) with 47–48 years as the reference group, and reproductive lifespan (classified as ≤28, 29–31, 32–34, 35–37, and ≥38 years) with 32–34 years as the reference group.

This study further investigated the associations by additionally adjusting for age at recruitment (continuous), BMI (continuous), waist circumference (continuous), ethnicity (Han or other ethnicities), region (urban or rural), marital status (unmarried/widowed, married/cohabiting), education level (elementary or below, junior high school, high school or above), alcohol drinking (yes or no), smoking (yes or no), pharmacological treatment (yes or no), comorbidity (yes or no), family history of CVD (yes or no), ever pregnant (yes or no), contraceptive use (yes or no), breastfeeding experience (yes or no), and parity (0–1, 2, ≥3). We also examined the CVD risk by age at menarche and menopause and reproductive lifespan in subgroups of women defined by region, age at recruitment, marital status, BMI, education level, comorbidity, pharmacological treatment, alcohol drinking status, and family history of CVD, use of contraceptives, parity.

R 3.6.2 software were used to conduct analyses. The threshold of statistical significance was set at p < 0.05.

Results

The characteristics of the study participants by age at menarche and menopause, and reproductive lifespan were listed in Tables 1–3, respectively. The mean (SD) age of study participants at recruitment was 63.6 (9.9) years, and the mean age at menarche and menopause, and reproductive lifespan were 15.9 (2.0), 48.7 (3.5), and 32.9 (3.9) years, respectively. The mean (SD) BMI, waist circumference, and parity were 24.8 (3.7) kg/m², 83.9 (10.4) cm, and 3.0 (2.3), respectively. A minority of women were smokers (3.8%), alcohol drinkers (5.5%), and users of contraceptives (8.0%). Most women had previously pregnant (99.1%) and breastfeeding experience (96.2%). Women with earlier age at menarche had higher educational level, had lower BMI, waist circumference and parity, had higher percent of urban resident. Women with later age at menopause had higher educational level, BMI, and waist circumference, had higher percent of comorbidity, Women with lower reproductive lifespan had higher parity, had lower educational level, BMI and waist circumference, had lower percent of comorbidity.

Figure 2 showed the HRs for CVD events by age at menarche, age at menopause, and reproductive lifespan amongst postmenopausal women. In model 1, the association between age at menarche and CVD was significant, and the association between age menopause, reproductive lifespan and CVD was not significant. In model 2 and 3, the association between age at menarche, reproductive lifespan and CVD was significant, and the association between age menopause and CVD was not significant. Model 3 showed that for those with age at menarche ≤ 13, 14, 15 (reference), 16, and ≥ 17 years, the HRs (95%CIs) were respectively 0.887 (0.489–1.609), 0.993 (0.560–1.762) 1.000 (reference), 1.157 (0.699–1.915), and 1.589 (1.041–2.424), for those with age at menopause ≤44, 45–46, 47–48 (reference), 49–50, and ≥51 years, the HRs (95%CIs) were respectively 1.388n(0.821–2.346), 0.861 (0.482–1.537), 1.000 (reference), 0.909 (0.587–1.405), and 1.111. (0.716–1.726), for those with reproductive lifespan ≤28, 29–31, 32–34 (reference), 35–37, and ≥38, the HRs (95%CIs) were respectively 1.368 (0.896–2.090), 1.059 (0.700–1.602), 1.000 (reference), 0.746 (0.492–1.132), and 0.926 (0.538–1.549). The highest risk was seen in those with menarche at age ≥17 years, and those with reproductive lifespan ≤28 years.

FIGURE 2

Age at menarche was positively associated with CVD events, with an adjusted HR (95%CI) of 1.106 (1.047–1.167) per year. For every 1-year increase in age at menarche, the risk of CVD increased by 10.6%. The association between age at menopause and risk of CVD was not significant, with an adjusted HR (95%CI) of 0.982 (0.943–1.024) per year. Reproductive lifespan was negatively associated with CVD events, with an adjusted HR (95%CI) of 0.962 (0.929–0.996) per year. For every 1-year increase in reproductive lifespan, the risk of CVD was reduced by 3.8%.

Subgroup analyses were also conducted according to region, age at recruitment, marital status, BMI, education level, pharmacological treatment, comorbidity, alcohol drinking status, use of contraceptives, parity, and family history of CVD (Figure 3). There was a positive association between age at menarche and risk of CVD events in postmenopausal women within the following subgroups: living in urban areas, 70 years old and above, low BMI, low education level, have no comorbidity, have pharmacological treatment, non-drinkers, no previous contraceptive use, and 0–2 live births. There was a negative association between reproductive lifespan and risk of CVD events among the following subgroups: married, 60–70 years old, low BMI, low education level, have comorbidity, have pharmacological treatment, non-drinkers, no previous contraceptive use, and 2 live births. There was a negative association between age at menopause and CVD risk in postmenopausal women with comorbidity, with an adjusted HR (95%CI) of 0.938 (0.880–0.999) per year. The risk of CVD reduced by 6.2% for every 1-year increase in age at menopause in postmenopausal women with comorbidity.

FIGURE 3

Discussion

To our knowledge, this was the first large prospective study that comprehensively investigated the associations between age at menarche and menopause, reproductive lifespan, and risk of CVD events in Chinese postmenopausal women using a nationally representative sample and evaluating multiple subgroups. Based on 6,198 Chinese postmenopausal women without prior history of CVD, we found that late age at menarche and shorter reproductive span is significantly associated with increased risk in CVD events among women. These associations also appeared to be similar amongst subgroups. There was also a negative association between age at menopause and CVD risk in postmenopausal women with comorbidity. For every 1-year increase in age at menarche, the risk of CVD increased by 10.6%, and for every 1-year increase in reproductive lifespan, the risk of CVD reduced by 3.8%. The risk of CVD reduced by 6.2% for every 1-year increase in age at menopause in women with comorbidity.

Several studies have previously investigated the relationship of age of menarche and CVD events, but reported inconsistent findings. A systematic review revealed that for Caucasian populations, eight out of twelve studies show a generally linear association between a decrease in age at menarche with an increase in CVD risk (11). But the UK Million Women Study showed a significant U-shaped relationship between age at menarche and the outcomes CHD (6). This discrepancy may be due in part to small sample sizes, geographic limits to one city or province, or only rural areas, age or ethnic differences, or residual confounding from unmeasured or other potential risk factors. The results from studies with Asian populations are inconclusive, with either early or late menarche increasing the CVD risk. One cohort study reported an increased risk of ischemic stroke for women with an age at menarche ≤13 years compared to those with 15 years, but the participants were selected from a rural town in northern Japan and therefore not representativeness of the general population (27). The same U-shape between age at menarche and CVD risk was found in data from the Chinese Kadoori Biobank (CKB), but the associations seemed to differ by birth cohort (28). A case-control study reported that higher age at menarche was associated with an increased ischemic stroke risk, which was consistent with our study (29).

Some mechanisms may explain the positive correlation between age of menarche and risk of CVD events in our results. Studies have shown that late menarche is associated with low estrogen levels (30, 31). Estrogen affects the elasticity of blood vessels and regulates the level of metabolic mediators such as lipids, inflammatory markers and the coagulation system (4). Estrogen has a protective effect on CVD in women by stimulating endothelial nitric oxide synthase, which mediates vasodilation and maintains cardiovascular health (32, 33). Women with early age at menarche are more likely to have higher levels of ovarian hormone, which can protect women from hypertension and atherosclerosis (34). Several studies agree about the different impact of testosterone on males and females (35, 36). Low endogen levels of this hormone in males can be associated with CVD and coronary stenosis severity. High levels of circulating androgens in women appear to be associated with higher cardiovascular risk (37, 38). In addition, age at menarche is associated with the higher adiposity both in childhood and in adulthood (39, 40). Adiposity indicators mediated the relationship between age at menarche and blood pressure in women. Adiposity is a risk factor of CVD, so the association between age at menarche and CVD could a result of higher estrogen levels or higher adiposity in early maturing women (40).

Additionally, the relationships between age at menopause and CVD risk in previous research are contradictory. Two meta-analysis indicated women with early menopausal age have a higher risk of incident CVD (16, 41). However, the result might have introduced some heterogeneity or has certain limitations about extrapolation due to the limited racial population included. Results of UK Biobank on early natural menopause were associated with a increased risk for a composite of CVD may have a “healthy participant” selection bias (42). The following studies are consistent with our findings on no convincing relationship between early menopausal age and cardiovascular disease (12, 43–47). Differences in population and study design and the influence of confounding factors may be the main reasons for the inconsistent results.

Persuasive evidence demonstrated that bilateral oophorectomy in premenopausal women increases the risk of CHD unless exogenous hormones are administered (48). However, there is no convincing evidence to support the hypothesis that natural menopause is a risk factor for CHD. When women with natural, surgical, and medicated menopause were analyzed together, the risk increased significantly with decreasing age at menopause, but this inverse association was limited to current non-smokers and not statistically significant amongst women with natural menopause (49). In a previous report from the Nurses’ Health Study, with further adjustment for smoking and age the relative risk of CHD in postmenopausal women diminished from significantly elevated to insignificant (48). These results might reflect the need to closely control the residual confounding factors of smoking and age, which have been adjusted for in our study. Furthermore, we found that there was a negative association between age at menopausal and CVD risk in postmenopausal women with comorbidity. As far as we know, diabetes, hypertension and dyslipidemia are independent risk factors for CVD events and show a additive association with the risk of CVD (50). Our finding suggests that this association may be more striking to particularly attention in postmenopausal women.

Previous studies investigating the association between reproductive lifespan and CVD risk were inconsistent. A systematic review and meta-analysis found that women with a shorter reproductive lifespan was associated with a higher risk of CVD events, with a 31% increased risk of stroke in particular (19). The Nurse’s Health Study found that the CVD risk was 25% higher amongst those with <30 years of reproductive lifespan compared to 34–37 years (51). One cross-sectional study from the United States showed that each yearly increase in reproductive lifespan was associated with 3% reduction in the risk for overall CVD and stroke events (20). The findings from this and other studies were consistent for CHD (34, 51, 52). A cohort study from the Women’s Health Initiative manifested that a shorter total reproductive duration in postmenopausal women resulted in a modestly increased risk of any heart failure (53). In Asia, the study of CKB found that total reproductive years were inversely associated with risks of both fatal and non-fatal CVD events, with 1.4% lower risk of CVD events death per each additional reproductive year (52). For stroke mortality, a large prospective study from Japan showed a decreased risk for longer reproductive lifespan (54). The above relationship between reproductive lifespan and CVD risk is consistent with our current study. However, some studies have found that there is no statistically significant association between the number of reproductive years and CVD mortality (9, 46, 55, 56). In addition, Jung et al. found a U-shaped association between reproductive lifespan and ischemic heart disease; the risk of which increased in both reproductive lifespan <30 and 40 years when 36–39 years were used as a reference (34). In one prospective study, it was significantly associated with 5% higher mortality for every additional year of reproductive lifespan (57).

Timing of menarche and menopause were correlated in that women who experienced early menarche were at higher risk of early menopause (51). In addition, reproductive lifespan can serve as a simple way to estimate estrogen exposure (51). Therefore, the underlying mechanism linking a longer reproductive lifespan with reduced risk of CVD events can be attributed to prolonged exposure to endogenous estrogen, which is accordant with our previous explanatory mechanism. These findings suggest that reproductive factors may play an important role in maintaining and improving cardiovascular health, which can be used to assess populations with poor cardiovascular health for targeted interventions.

Strengths and Limitations

Important strengths of our study are the prospective design and nationally representative sample. The study has several other strengths, including the standardized approaches and stringent quality control measures taken to ensure data quality and reliability. We adjusted for potential risk factors for CVD and conducted a detailed subgroup analysis to improve the reliability of our results, which allowed us to simultaneously adjust for potential confounders and reliably assess the associations.

Several limitations need to be taken into account. First, CVD is composed of multiple diseases, so it is unclear whether role in our study is specific for certain CVD. Second, age at menarche is known to vary by ethnicity, with girls of African and Asian descent experiencing earlier menarche than Caucasian girls (58, 59). However, it is unknown whether ethnicity plays a role in the association between age at menarche and CVD events. Furthermore, our study participants were Chinese women, which minimized the confounding effects by ethnic background, but might reduce the generalization of our results to other ethnic groups. Thirdly, ages at the time of menarche and menopause were self-reported which raises the possibility of misclassification due to recall bias. However, previous studies have reported that the recall of age at menarche (60, 61) and menopause is relatively accurate (62, 63). Therefore, self-reported age at menarche and menopause were reasonably valid and reproducible. If recall bias existed, it would be non-differential, tending to attenuate the real strengths of the associations that we observed. Lastly, although we have adjusted for a comprehensive range of potential confounders, the possibility of residual confounding from other known or unknown risk factors cannot be completely ruled out.

Conclusion

Based on 6,198 Chinese postmenopausal women who had no prior history of CVD, we found that late age at menarche and shorter reproductive span are both significantly associated with increased risk of CVD events. These associations also appeared to be similar amongst subgroups. In addition, there was a negative association between age at menopause and CVD risk in postmenopausal women with comorbidity. Our findings have important public health implications for early detection and timely implementation of appropriate interventions in women at high risk of CVD.

References

• 1.

  YangGWangYZengYGaoGFLiangXZhouMet alRapid health transition in China, 1990-2010: findings from the Global burden of disease study 2010.Lancet. (2013) 381:1987–2015. 10.1016/S0140-6736(13)61097-1

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 2.

  AbubakarITillmannTBanerjeeA. Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013.Lancet. (2015) 385:117–71. 10.1016/S0140-6736(14)61682-2

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 3.

  World Health Organization [WHO]. Noncommunicable Diseases. Country Profiles 2018. (2018). Available online at: https://www.who.int/publications/i/item/9789241514620(accessed March 29, 2022).

  • Google Scholar

• 4.

  MaasAHAppelmanYE. Gender differences in coronary heart disease.Neth Heart J. (2010) 18:598–603.

  • Google Scholar

• 5.

  DiVallSARadovickS. Pubertal development and menarche.Ann N Y Acad Sci. (2008) 1135:19–28.

  • Google Scholar

• 6.

  CanoyDBeralVBalkwillAWrightFLKrollMEReevesGKet alAge at menarche and risks of coronary heart and other vascular diseases in a large UK Cohort.Circulation. (2015) 131:237–44. 10.1161/CIRCULATIONAHA.114.010070

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 7.

  CharalampopoulosDMcLoughlinAElksCEOngKKet alAge at menarche and risks of all-cause and cardiovascular death: a systematic review and meta-analysis.Am J Epidemiol. (2014) 180:29–40. 10.1093/aje/kwu113

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 8.

  ColditzGAWillettWCStampferMJRosnerBSpeizerFEHennekensCH. A prospective study of age at menarche, parity, age at first birth, and coronary heart disease in women.Am J Epidemiol. (1987) 126:861–70.

  • Google Scholar

• 9.

  CuiRIsoHToyoshimaHDateCYamamotoAKikuchiSet alRelationships 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. 10.2188/jea.16.177

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 10.

  ZhuDIsoHToyoshimaHDateCYamamotoAKikuchiSet alAge at natural menopause and risk of incident cardiovascular disease: a pooled analysis of individual patient data.Lancet Public Health. (2019) 4:e553–64. 10.1016/S2468-2667(19)30155-0

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 11.

  LuijkenJvan der SchouwYTMensinkDOnland-MoretNC. Association between age at menarche and cardiovascular disease: a systematic review on risk and potential mechanisms.Maturitas. (2017) 104:96–116.

  • Google Scholar

• 12.

  SnowdonDAKaneRLBeesonWLBurkeGLSprafkaJMPotterJet alIs early natural menopause a biologic marker of health and aging?.Am J Public Health. (1989) 79:709–14.

  • Google Scholar

• 13.

  CarrMC. The emergence of the metabolic syndrome with menopause.J Clin Endocrinol Metab. (2003) 88:2404–11.

  • Google Scholar

• 14.

  AgrinierACournotMDallongevilleJArveilerDDucimetièrePRuidavetsJBet alMenopause and modifiable coronary heart disease risk factors: a population based study - ScienceDirect.Maturitas. (2010) 65:237–43. 10.1016/j.maturitas.2009.11.023

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 15.

  TothMJChernofASitesCKPoehlmanET. Effect of menopausal status on body composition and abdominal fat distribution.Int J Obes Relat Metab Disord. (2000) 24:226–31.

  • Google Scholar

• 16.

  MukaTOliver-WilliamsCKunutsorSLavenJSFauserBCChowdhuryRet alAssociation of age at onset of menopause and time since onset of menopause with cardiovascular outcomes, intermediate vascular traits, and all-cause mortality: a systematic review and meta-analysis.JAMA Cardiol. (2016) 1:767–76. 10.1001/jamacardio.2016.2415

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 17.

  KimSHSimMYParkSB. Association between duration of reproductive lifespan and Framingham risk score in postmenopausal women.Maturitas. (2015) 82:431–5. 10.1016/j.maturitas.2015.07.011

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 18.

  MishraSRWallerMChungHFMishraGD. Association of the length of oestrogen exposure with risk of incident stroke in postmenopausal women: insights from a 20-year prospective study.Int J Cardiol. (2021) 328:206–14. 10.1016/j.ijcard.2020.12.022

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 19.

  MishraSRHungHFWallerMMishraGD. Duration of estrogen exposure during reproductive years, age at menarche and age at Menopause, and risk of cardiovascular disease events, all−cause and cardiovascular mortality: a systematic review and meta−analysis.BJOG. (2021) 128:809–21. 10.1111/1471-0528.16524

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 20.

  MansoorHElgendyIYSegalRHartzemaA. Duration of reproductive years and the risk of cardiovascular and cerebrovascular events in older women: insights from the national health and nutrition examination survey.J Womens Health. (2017) 26:1047–52. 10.1089/jwh.2016.6013

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 21.

  KatzmarzykPTChurchTSJanssenIRossRBlairSN. Metabolic syndrome, obesity, and mortality: impact of cardiorespiratory fitness.Diabetes Care. (2005) 28:391–7.

  • Google Scholar

• 22.

  DongYWangXZhangLChenZZhengCWangJet alHigh-sensitivity C reactive protein and risk of cardiovascular disease in China-CVD study.J Epidemiol Community Health. (2019) 73:188–92.

  • Google Scholar

• 23.

  WangZChenZZhangLWangXHaoGZhangZet alStatus of hypertension in china: results from the China hypertension survey, 2012-2015.Circulation. (2018) 137:2344–56.

  • Google Scholar

• 24.

  Joint Committee on Guidelines for Prevention and Treatment of dyslipidemia in adults in China. Chinese guidelines for prevention and treatment of dyslipidemia in adults [J]. Chin J cardiol. (2007) 35:390–419.

  • Google Scholar

• 25.

  ZhangDTangXShenPSiYLiuXXuZet alMultimorbidity of cardiometabolic diseases: prevalence and risk for mortality from one million Chinese adults in a longitudinal cohort study.BMJ Open. (2019) 9:e024476. 10.1136/bmjopen-2018-024476

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 26.

  LiuG.Relationship between Age of Menarche and Live Birth and Obesity and Hypertension in Women.Chongqing: Chongqing Medical University (2019).

  • Google Scholar

• 27.

  MurakamiKMetokiHSatohMAsayamaKHosakaMMatsudaAet alMenstrual factors and stroke incidence in Japanese postmenopausal women: the Ohasama study.Neuroepidemiology. (2016) 2016:109–16. 10.1159/000452220

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 28.

  YangLLiLMillwoodIYPetersSAEChenYGuoYet alAge at menarche and risk of major cardiovascular diseases: evidence of birth cohort effects from a prospective study of 300,000 Chinese women.Int J Cardiol. (2017) 227:497–502. 10.1016/j.ijcard.2016.10.115

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 29.

  HsiehYCHwangL-CHsiehF-ILienLMLinH-JHuC-Jet alEarly menarche and ischemic stroke risk among postmenopausal women.Int J Gerontol. (2010) 4:16–22. 10.1212/01.wnl.0000250238.69938.f5

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 30.

  QiuCChenHWenJZhuPLinFHuangBet alAssociations between age at menarche and menopause with cardiovascular disease, diabetes, and osteoporosis in Chinese women.J Clin Endocrinol Metab. (2013) 98:1612–21. 10.1210/jc.2012-2919

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 31.

  KleijnMJJDSchouwYTVDGraafYVD. Reproductive history and cardiovascular disease risk in postmenopausal women - A review of the literature.Maturitas. (1999) 33:7–36.

  • Google Scholar

• 32.

  ChenZYuhannaISGalcheva-GargovaZKarasRHMendelsohnMEShaulPW. Estrogen receptor a mediates the nongenomic activation of endothelial nitric oxide synthase by estrogen.J Clin Invest. (1999) 103:401–6.

  • Google Scholar

• 33.

  DubeyRKOparilSImthurnBJacksonEK. Sex hormones and hypertension.Cardiovasc Res. (2002) 53:688–708.

  • Google Scholar

• 34.

  JungKJKimMRYunYDKimHCJeeSH. Duration of ovarian hormone exposure and atherosclerotic cardiovascular disease in Korean women: the Korean Heart Study.Menopause. (2016) 23:60–6. 10.1097/GME.0000000000000489

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 35.

  WuFCvon EckardsteinA. Androgens and coronary artery disease.Endocr Rev. (2003) 24:183–217.

  • Google Scholar

• 36.

  HuXRuiLZhuTXiaHYangXWangXet alLow testosterone level in middle-aged male patients with coronary artery disease.Eur J Intern Med. (2011) 22:e133–6.

  • Google Scholar

• 37.

  AlexanderCJTangchitnobEPLeporNE. Polycystic ovary syndrome: a major unrecognized cardiovascular risk factor in women.Rev Cardiovasc Med. (2009) 10:83–90.

  • Google Scholar

• 38.

  ChristakouCDDiamanti-KandarakisE. Role of androgen excess on metabolic aberrations and cardiovascular risk in women with polycystic ovary syndrome.Womens Health. (2008) 4:583–94. 10.2217/17455057.4.6.583

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 39.

  CastilhoSDNucciLB. Age at menarche in schoolgirls with and without excess weight.J Pediatr. (2015) 91:75–80. 10.1016/j.jped.2014.05.008

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 40.

  WerneckAOOyeyemiALCyrinoESRonqueERVSzwarcwaldCLet alAssociation between age at menarche and blood pressure in adulthood: is obesity an important mediator?.Hypertens Res. (2018) 41:856–64.

  • Google Scholar

• 41.

  Roeters van LennepJEHeidaKYBotsMLHoekACollaborators Dutch.Cardiovascular disease risk in women with premature ovarian insufficiency: a systematic review and meta-analysis.Eur J Prev Cardiol. (2016) 23:178–86.

  • Google Scholar

• 42.

  HonigbergMCZekavatSMAragamKFinneranPKlarinDBhattDLet alAssociation of premature natural and surgical menopause with incident cardiovascular disease.JAMA. (2019) 322:2411–21.

  • Google Scholar

• 43.

  HuanLDengXHeMChenSNiuW. Meta-analysis: early age at natural menopause and risk for all-cause and cardiovascular mortality.Biomed Res Int. (2021) 2021:6636856.

  • Google Scholar

• 44.

  GongDSunJZhouYZouCFanY. Early age at natural menopause and risk of cardiovascular and all-cause mortality: a meta-analysis of prospective observational studies.Int J Cardiol. (2016) 203:115–9. 10.1016/j.ijcard.2015.10.092

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 45.

  AtsmaFBartelinkMLGrobbeeDEvan der SchouwYT. Postmenopausal status and early menopause as independent risk factors for cardiovascular disease: a meta-analysis.Menopause. (2006) 13:265–79. 10.1097/01.gme.0000218683.97338.ea

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 46.

  WuXCaiHKallianpurAGaoYTYangGChowWHet alAge at menarche and natural menopause and number of reproductive years in association with mortality: results from a median follow-up of 11.2 years among 31,955 naturally menopausal Chinese women.PLoS One. (2014) 9:e103673. 10.1371/journal.pone.0103673

  • CrossRef
  • Google Scholar

• 47.

  GallagherLGDavisLBRayRMPsatyBMGaoDLCheckowayHet alReproductive history and mortality from cardiovascular disease among women textile workers in Shanghai, China.Int J Epidemiol. (2011) 40:1510–8. 10.1093/ije/dyr134

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 48.

  ColditzGAWillettWCStampferMJRosnerBSpeizerFEHennekensCH. Menopause and the risk of coronary heart disease in women.N Engl J Med. (1987) 316:1105–10.

  • Google Scholar

• 49.

  van der SchouwYTvan der GraafYSteyerbergEWEijkemansJCBangaJD. Age at menopause as a risk factor for cardiovascular mortality.Lancet. (1996) 347:714–8.

  • Google Scholar

• 50.

  WangJWangZGuoFZhangYJiHChenGet alIndividual and Combined Cardiometabolic Morbidities and the Subsequent Risk of Cardiovascular Events in Chinese Adults.J Clin Endocrinol Metab. (2022) 107:e84–94. 10.1210/clinem/dgab609

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 51.

  LeySHLiYTobiasDKMansonJERosnerBHuFBet alDuration of reproductive life span, age at menarche, and age at menopause are associated with risk of cardiovascular disease in women.J Am Heart Assoc. (2017) 6:e006713.

  • Google Scholar

• 52.

  LingYLinLKartsonakiCGuoYChenYBianZet alMenopause characteristics, total reproductive years, and risk of cardiovascular disease among Chinese women.Circ Cardiovasc Qual Outcomes. (2017) 10:e004235.

  • Google Scholar

• 53.

  HallPSNahGHowardBVLewisCEAllisonMASartoGEet alReproductive factors and incidence of heart failure hospitalization in the Women’s Health Initiative.J Am Coll Cardiol. (2017) 69:2517–26.

  • Google Scholar

• 54.

  OtsukiSSaitoESawadaNAbeSKHidakaAYamajiTet alFemale reproductive factors and risk of all-cause and cause-specific mortality among women: the Japan public health center–based prospective study (JPHC study).Ann Epidemiol. (2018) 28:597–604.e6. 10.1016/j.annepidem.2018.06.001

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 55.

  ChangHSOdonguaNOhrrHSullJWNamCM. Reproductive risk factors for cardiovascular disease mortality among postmenopausal women in Korea: the Kangwha Cohort Study, 1985-2005.Menopause. (2011) 18:1205–12. 10.1097/gme.0b013e31821adb43

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 56.

  JansenSCTemmeEHSchoutenEG. Lifetime estrogen exposure versus age at menopause as mortality predictor.Maturitas. (2002) 43:105–12. 10.1016/s0378-5122(02)00183-4

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 57.

  JaspersLKavousiMErlerNSHofmanALavenJSFrancoOH. Fertile lifespan characteristics and all-cause and cause-specific mortality among postmenopausal women: the Rotterdam Study.Fertil Steril. (2017) 107:448–456.e110.1016/j.fertnstert.2016.11.006

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 58.

  FreedmanDSKhanLKSerdulaMKDietzWHSrinivasanSRBerensonGS. Relation of age at menarche to race, time period, and anthropometric dimensions: the Bogalusa Heart Study.Pediatrics. (2002) 110:e43. 10.1542/peds.110.4.e43

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 59.

  YermachenkoADvornykV. Nongenetic determinants of age at menarche: a systematic review.BioMed Res Int. (2014) 2014:371583. 10.1155/2014/371583

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 60.

  MustAPhillipsSMNaumovaENBlumMHarrisSDawson-HughesBet alRecall of early menstrual history and menarcheal body size: after 30 years, how well do women remember?.Am J Epidemiol. (2002) 155:672–9. 10.1093/aje/155.7.672

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 61.

  CaseyVDwyerJTColemanKAKrallEAGardnerJValadianIet alAccuracy of recall by middle-aged participants in a longitudinal study of their body size and indices of maturation earlier in life.Ann Hum Biol. (1991) 18:155–66. 10.1080/03014469100001492

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 62.

  ColditzGAStampferMJWillettWCStasonWBRosnerBHennekensCHet alReproducibility and validity of self-reported menopausal status in a prospective cohort study.Am J Epidemiol. (1987) 126:319–25. 10.1093/aje/126.2.319

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 63.

  Den TonkelaarI. Validity and reproducibility of self-reported age at menopause in women participating in the DOM-project.Maturitas. (1997) 27:117–23. 10.1016/s0378-5122(97)01122-5

  • Pubmed Abstract
  • CrossRef
  • Google Scholar