4.6 Article

Premenopausal cardiovascular disease and age at natural menopause: a pooled analysis of over 170,000 women

期刊

EUROPEAN JOURNAL OF EPIDEMIOLOGY
卷 34, 期 3, 页码 235-246

出版社

SPRINGER
DOI: 10.1007/s10654-019-00490-w

关键词

Premenopausal; Cardiovascular disease; Age at menopause; Pooled analysis

资金

  1. Australian National Health and Medical Research Council Project Grant [APP1027196]
  2. Australian National Health and Medical Research Council Principal Research Fellowship [APP1121844]

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Early menopause is associated with an increased risk of subsequent cardiovascular disease (CVD). Few studies have investigated the converse. We examined whether premenopausal CVD events are associated with early age at menopause. We pooled the individual data of 177,131 women from nine studies. We used multinomial logistic regression models to estimate multivariable relative risk ratios (RRR) and 95% confidence intervals (CI) for the associations between age at onset of premenopausal CVD eventsincluding coronary heart disease (CHD) and strokeand age at natural menopause. Altogether 1561 (0.9%) premenopausal participants reported CVD events (including 1130 CHD and 469 stroke) at a mean age of 41.3years. Compared with women without any premenopausal CVD events, women who experienced a first CVD event before age 35years had a twofold risk of menopause before age 45years (early menopause); adjusted RRR (95% CI) of 1.92 (1.17, 3.14) for any CVD, 1.86 (1.01, 3.43) for CHD and 2.17 (1.43, 3.30) for stroke. Women who experienced a first premenopausal CVD event after age 40years underwent a natural menopause at the expected age (around 51years). These associations were robust to adjustment for smoking status, BMI, educational level, race/ethnicity, age at menarche, parity, hypertension and family history of CVD. For premenopausal women, a first CVD event before age 35years is associated with a doubling of the risk of an early menopause, while a first CVD event occurred after 35years indicates a normal menopause at around 51years. Shared genetic and environmental factors (such as smoking), as well as compromised vasculature following CVD events, may contribute to this outcome.

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