The variability of female reproductive ageing

被引:868
作者
Velde, ERT [1 ]
Pearson, PL
机构
[1] Univ Utrecht, Med Ctr, Dept Reprod Med, NL-3508 GA Utrecht, Netherlands
[2] Univ Utrecht, Med Ctr, Dept Med Genet, NL-3508 GA Utrecht, Netherlands
关键词
age at last birth; age at menopause; delayed childbearing; genetic control; reproductive ageing;
D O I
10.1093/humupd/8.2.141
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The delay in childbearing is an important societal change contributing to an increasing incidence of subfertility. The prevailing concept of female reproductive ageing assumes that the decline of both quantity and quality of the oocyte/follicle pool determines an age-dependent loss of female fertility. There is an apparent discrepancy between the ability to maintain a regular ovulatory cycle pattern and the several years earlier cessation of female fertility. This latter is largely explained by an age-related increase of meiotic non-disjunction leading to chromosomal aneuploidy and early pregnancy loss, such that most embryos from women greater than or equal to40 years old are chromosomally abnormal and rarely develop further. The final stage of reproductive ageing-the occurrence of menopause shows a huge variation between women. Age at last birth in natural fertility populations, which marks the end of female fertility, shows an identically wide variation as age at menopause, but occurs on average 10 years earlier. Given the high heritability for age at menopause, the variation in both age of menopause and last birth are probably under genetic control by the same set of genes. Some of those genes must carry heritable variants which modulate the rate of ovarian ageing and give rise to the wide age variations for the various phases of reproductive ageing.
引用
收藏
页码:141 / 154
页数:14
相关论文
共 213 条
[1]  
Abma J C, 1997, Vital Health Stat 23, P1
[2]   Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene [J].
Aittomaki, K ;
Herva, R ;
Stenman, UH ;
Juntunen, K ;
Ylostalo, P ;
Hovatta, O ;
delaChapelle, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (10) :3722-3726
[3]  
Allingham-Hawkins SJ, 1999, AM J MED GENET, V83, P322, DOI 10.1002/(SICI)1096-8628(19990402)83:4<322::AID-AJMG17>3.0.CO
[4]  
2-B
[5]   MALE AGE AND FERTILITY RESULTS FROM IRELAND PRIOR TO 1911 [J].
ANDERSON, BA .
POPULATION INDEX, 1975, 41 (04) :561-567
[6]   First-meiotic-division nondisjunction in human oocytes [J].
Angell, R .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (01) :23-32
[7]  
[Anonymous], 1977, Human Fertility: The Basic Components
[8]  
BAIRD DD, 1988, P SOC EPIDEMIOL RES, V1, P907
[9]   A QUANTITATIVE AND CYTOLOGICAL STUDY OF GERM CELLS IN HUMAN OVARIES [J].
BAKER, TG .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1963, 158 (972) :417-+
[10]   Predictors of poor ovarian response in in vitro fertilization: a prospective study comparing basal markers of ovarian reserve [J].
Bancsi, LFJMM ;
Broekmans, FJM ;
Eijkemans, MJC ;
de Jong, FH ;
Habbema, JDF ;
te Velde, ER .
FERTILITY AND STERILITY, 2002, 77 (02) :328-336