Age at natural menopause in women exposed to diethylstilbestrol in utero

被引:53
|
作者
Hatch, Elizabeth E.
Troisi, Rebecca
Wise, Lauren A.
Hyer, Marianne
Palmer, Julie R.
Titus-Ernstoff, Linda
Strohsnitter, William
Kaufman, Raymond
Adam, Ervin
Noller, Kenneth L.
Herbst, Arthur L.
Robboy, Stanley
Hartge, Patricia
Hoover, Robert N.
机构
[1] Boston Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[2] NCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[3] Boston Univ, Slone Epidemiol Ctr, Boston, MA 02215 USA
[4] Informat Management Serv Inc, Rockville, MD USA
[5] Dartmouth Hitchcock Med Ctr, Norris Cotton Canc Ctr, Lebanon, NH 03766 USA
[6] Tufts Univ New England Med Ctr, Dept Obstet & Gynecol, Boston, MA USA
[7] Baylor Coll Med, Dept Obstet & Gynecol, Houston, TX 77030 USA
[8] Univ Chicago, Dept Obstet & Gynecol, Chicago, IL 60637 USA
[9] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[10] Duke Univ, Med Ctr, Dept Obstet & Gynecol, Durham, NC 27710 USA
关键词
diethylstilbestrol; longitudinal studies; menopause; prenatal exposure delayed effects; survival analysis;
D O I
10.1093/aje/kwj257
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Age at natural menopause is related to several health outcomes, including cardiovascular disease and overall mortality. Age at menopause may be influenced by the number of follicles formed during gestation, suggesting that prenatal factors could influence menopausal age. Diethylstilbestrol (DES), a nonsteroidal estrogen widely prescribed during the 1950s and 1960s, is related to reproductive tract abnormalities, infertility, and vaginal cancer in prenatally exposed daughters but has not been studied in relation to age at menopause. The authors used survival analyses to estimate the risk of natural menopause in 4,210 DES-exposed versus 1,829 unexposed US women based on responses to questionnaires mailed in 1994, 1997, and 2001. DES-exposed women were 50% more likely to experience natural menopause at any given age (hazard ratio = 1.49, 95% confidence interval: 1.28, 1.74). Among women for whom dose information was complete, there were dose-response effects, with a greater than twofold risk for those exposed to > 10,000 mg. The causal mechanism for earlier menopause may be related to a smaller follicle pool, more rapid follicle depletion, or changes in hormone synthesis and metabolism in DES-exposed daughters. Age at menopause has been related, albeit inconsistently, to several exposures, but, to the authors' knowledge, this is the first study to suggest that a prenatal exposure may influence reproductive lifespan.
引用
收藏
页码:682 / 688
页数:7
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