Genomic Markers of Ovarian Reserve

被引:49
作者
Wood, Michelle A. [1 ]
Rajkovic, Aleksandar [1 ,2 ,3 ]
机构
[1] Univ Pittsburgh, Magee Womens Res Inst, Dept Obstet Gynecol & Reprod Sci, Pittsburgh, PA USA
[2] Univ Pittsburgh, Dept Pathol, Magee Womens Res Inst, Pittsburgh, PA USA
[3] Univ Pittsburgh, Dept Human Genet, Magee Womens Res Inst, Pittsburgh, PA USA
关键词
ovarian reserve; menopause; premature ovarian failure; GROWTH-DIFFERENTIATION FACTOR-9; STIMULATING-HORMONE RECEPTOR; ANTI-MULLERIAN HORMONE; DNA-DAMAGE CHECKPOINT; NATURAL MENOPAUSE; TRANSCRIPTION FACTOR; X-CHROMOSOME; MENTAL-RETARDATION; GENE POLYMORPHISMS; WIDE ASSOCIATION;
D O I
10.1055/s-0033-1356476
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Ovarian reserve and its utilization, over a reproductive life span, are determined by genetic, epigenetic, and environmental factors. The establishment of the primordial follicle pool and the rate of primordial follicle activation have been under intense study to determine genetic factors that affect reproductive lifespan. Much has been learned from transgenic animal models about the developmental origins of the primordial follicle pool and mechanisms that lead to primordial follicle activation, folliculogenesis, and the maturation of a single oocyte with each menstrual cycle. Recent genome-wide association studies on the age of human menopause have identified approximately 20 loci, and shown the importance of factors involved in double-strand break repair and immunology. Studies to date from animal models and humans show that many genes determine ovarian aging, and that there is no single dominant allele yet responsible for depletion of the ovarian reserve. Personalized genomic approaches will need to take into account the high degree of genetic heterogeneity, family pedigree, and functional data of the genes critical at various stages of ovarian development to predict women's reproductive life span.
引用
收藏
页码:399 / 415
页数:17
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