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非裔美国女性 2 型糖尿病易感基因座的混合映射和精细映射。

Admixture mapping and fine-mapping of type 2 diabetes susceptibility loci in African American women.

机构信息

Escuela de Biología, Universidad de Costa Rica, San Pedro, Costa Rica.

Slone Epidemiology Center at Boston University, Boston, MA, USA.

出版信息

J Hum Genet. 2018 Nov;63(11):1109-1117. doi: 10.1038/s10038-018-0503-2. Epub 2018 Aug 22.

Abstract

African American women are disproportionately affected by type 2 diabetes. Genetic factors may explain part of the excess risk. More than 100 genetic variants have been associated with risk of type 2 diabetes, but most studies have been conducted in white populations. Two genome-wide association studies (GWAS) in African Americans have identified three novel genetic variants only. We conducted admixture mapping using 2918 ancestral informative markers in 2632 cases of type 2 diabetes, and 2596 controls nested in the ongoing Black Women's Health Study cohort, with the goal of identifying genomic loci with local African ancestry associated with type 2 diabetes. In addition, we performed replication analysis of 71 previously identified index SNPs, and fine-mapped those genetic loci to identify better or new genetic variants associated with type 2 diabetes in African Americans. We found that individual African ancestry was associated with higher risk of type 2 diabetes. In addition, we identified two genomic regions, 3q26 and 12q23, with excess of African ancestry associated with higher risk of type 2 diabetes. Lastly, we replicated 8 out of 71 index SNPs from previous GWAS, including, for the first time in African Americans, the X-linked rs5945326 SNP near the DUSP9 gene. In addition, our fine-mapping efforts suggest independent signals at five loci. Our detailed analysis identified two genomic regions associated with risk of type 2 diabetes, and showed that many genetic risk variants are shared across ancestries.

摘要

非裔美国女性患 2 型糖尿病的比例不成比例。遗传因素可能解释了部分超额风险。已经发现超过 100 种遗传变异与 2 型糖尿病的风险相关,但大多数研究都是在白人群体中进行的。两项针对非裔美国人的全基因组关联研究(GWAS)仅确定了三个新的遗传变异。我们使用 2918 个祖先信息标记对 2632 例 2 型糖尿病病例和 2596 例嵌套在正在进行的黑人妇女健康研究队列中的对照进行了混合映射,目的是确定与 2 型糖尿病相关的具有局部非洲血统的基因组基因座。此外,我们对之前确定的 71 个索引 SNP 进行了复制分析,并对这些遗传基因座进行了精细映射,以确定更好或新的与非裔美国人 2 型糖尿病相关的遗传变异。我们发现个体的非洲血统与 2 型糖尿病的风险增加有关。此外,我们确定了两个基因组区域,3q26 和 12q23,这些区域的非洲血统过多与 2 型糖尿病的风险增加有关。最后,我们复制了之前 GWAS 中的 71 个索引 SNP 中的 8 个,包括首次在非裔美国人中发现的 X 连锁 rs5945326 基因附近的 DUSP9 基因。此外,我们的精细映射工作表明在五个基因座上存在独立的信号。我们的详细分析确定了两个与 2 型糖尿病风险相关的基因组区域,并表明许多遗传风险变异在不同种族中是共享的。

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