Genetics of polycystic ovary syndrome

被引:32
作者
Franks, S
Gharani, N
Waterworth, D
Batty, S
White, D
Williamson, R
McCarthy, M
机构
[1] St Marys Hosp, Imperial Coll, Sch Med, Dept Obstet & Gynaecol, London W2 1PG, England
[2] St Marys Hosp, Imperial Coll, Sch Med, Dept Biochem & Mol Genet, London W2 1PG, England
[3] St Marys Hosp, Imperial Coll, Sch Med, Unit Metab Med, London W2 1PG, England
关键词
polycystic ovary syndrome; insulin; theca cells;
D O I
10.1016/S0303-7207(98)00178-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have found evidence for the involvement of two major genes in the aetiology of PCOS. The results of both linkage and association studies suggest that CYP11a (coding for P450 cholesterol side chain cleavage) and the insulin VNTR regulatory polymorphism are important genes in the aetiology of PCOS and may explain, in part, the heterogeneity of the syndrome. Differences in expression of CYP11a could account for variation in androgen production in women who have polycystic ovaries and those subjects who are homozygous for III alleles at the insulin gene VNTR locus are more likely to be hyperinsulinaemic. It is likely that other genes are involved in the aetiology of PCOS. Recent results lend weight to the idea that PCOS represents a complex trail in which several genes-but perhaps a relatively small number of key genes-contribute, in conjunction with nutritional factors, to the observed clinical and biochemical heterogeneity. (C) 1998 Published by Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:123 / 128
页数:6
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