Department of Internal Medicine, Erasmus MC, Rotterdam, The Netherlands.
Nat Genet. 2012 Jan 22;44(3):260-8. doi: 10.1038/ng.1051.
To newly identify loci for age at natural menopause, we carried out a meta-analysis of 22 genome-wide association studies (GWAS) in 38,968 women of European descent, with replication in up to 14,435 women. In addition to four known loci, we identified 13 loci newly associated with age at natural menopause (at P < 5 × 10(-8)). Candidate genes located at these newly associated loci include genes implicated in DNA repair (EXO1, HELQ, UIMC1, FAM175A, FANCI, TLK1, POLG and PRIM1) and immune function (IL11, NLRP11 and PRRC2A (also known as BAT2)). Gene-set enrichment pathway analyses using the full GWAS data set identified exoDNase, NF-κB signaling and mitochondrial dysfunction as biological processes related to timing of menopause.
为了新鉴定与自然绝经年龄相关的基因座,我们对 38968 名欧洲裔女性进行了 22 项全基因组关联研究(GWAS)的荟萃分析,并在最多 14435 名女性中进行了复制。除了四个已知的基因座外,我们还鉴定了 13 个与自然绝经年龄相关的新基因座(P < 5 × 10(-8))。位于这些新关联基因座的候选基因包括涉及 DNA 修复(EXO1、HELQ、UIMC1、FAM175A、FANCI、TLK1、POLG 和 PRIM1)和免疫功能(IL11、NLRP11 和 PRRC2A(也称为 BAT2))的基因。使用全 GWAS 数据集进行的基因集富集通路分析鉴定了外切核酸酶、NF-κB 信号和线粒体功能障碍作为与绝经时间相关的生物学过程。