The ovarian dysgenesis syndrome

被引:59
作者
Louis, G. M. Buck [1 ]
Cooney, M. A. [1 ]
Peterson, C. M. [2 ]
机构
[1] NICHHD, Div Epidemiol Stat & Prevent Res, Rockville, MD 20852 USA
[2] Univ Utah, Hlth Sci Ctr, Div Reprod Endocrinol & Infertil, Dept Obstet & Gynecol, Salt Lake City, UT USA
关键词
early origins; exposome; ovarian dysgenesis; HIGH PLASMA-CONCENTRATIONS; BREAST-CANCER; FETAL-GROWTH; POLYCHLORINATED-BIPHENYLS; ENDOMETRIAL CANCER; TESTICULAR CANCER; UTERINE LEIOMYOMA; BISPHENOL-A; IN-UTERO; ORGANOCHLORINE COMPOUNDS;
D O I
10.1017/S2040174410000693
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
New thinking has arisen about the origin of adult onset diseases stemming from a collective body of evidence commonly referred to as the developmental origins of health and disease. This conceptual paradigm posits that certain adult onset diseases arise during critical or sensitive windows of human development or even transgenerationally. The testicular dysgenesis hypothesis (TDS) postulates an in utero origin for adverse male reproductive outcomes, and is an excellent example of the early origins of the paradigm. Despite similarities in the development of the male and female reproductive tracks, noticeably absent is a collective body of evidence focusing on the plausibility of an early origin for gynecologic outcomes and later onset of adult diseases. Using the TDS paradigm, we synthesized the available literature relative to the ovarian dysgenesis syndrome (ODS), which we define as alterations in ovarian structure or function that may manifest as fecundity impairments, gynecologic disorders, gravid diseases or later onset adult diseases. We evaluated environmental exposures, particularly the role of endocrine disrupting chemicals, in relation to these outcomes, and found evidence (although fragmented) consistent with an in utero origin of gynecologic outcomes, which in turn is associated with later onset of adult diseases. The findings are interpreted within the ODS paradigm while delineating methodological challenges and future research opportunities designed to answer critical data gaps regarding the origin of fecundity, gravid health and chronic diseases affecting the female population.
引用
收藏
页码:25 / 35
页数:11
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