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全基因组关联研究冠心病及其风险因素在 8090 名非裔美国人:美国国立卫生研究院 CARe 项目。

Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

机构信息

Montreal Heart Institute, Montréal, Canada.

出版信息

PLoS Genet. 2011 Feb 10;7(2):e1001300. doi: 10.1371/journal.pgen.1001300.

Abstract

Coronary heart disease (CHD) is the leading cause of mortality in African Americans. To identify common genetic polymorphisms associated with CHD and its risk factors (LDL- and HDL-cholesterol (LDL-C and HDL-C), hypertension, smoking, and type-2 diabetes) in individuals of African ancestry, we performed a genome-wide association study (GWAS) in 8,090 African Americans from five population-based cohorts. We replicated 17 loci previously associated with CHD or its risk factors in Caucasians. For five of these regions (CHD: CDKN2A/CDKN2B; HDL-C: FADS1-3, PLTP, LPL, and ABCA1), we could leverage the distinct linkage disequilibrium (LD) patterns in African Americans to identify DNA polymorphisms more strongly associated with the phenotypes than the previously reported index SNPs found in Caucasian populations. We also developed a new approach for association testing in admixed populations that uses allelic and local ancestry variation. Using this method, we discovered several loci that would have been missed using the basic allelic and global ancestry information only. Our conclusions suggest that no major loci uniquely explain the high prevalence of CHD in African Americans. Our project has developed resources and methods that address both admixture- and SNP-association to maximize power for genetic discovery in even larger African-American consortia.

摘要

冠心病(CHD)是导致非裔美国人死亡的主要原因。为了确定与 CHD 及其危险因素(LDL-和 HDL-胆固醇(LDL-C 和 HDL-C)、高血压、吸烟和 2 型糖尿病)相关的常见遗传多态性,我们在来自五个基于人群的队列的 8090 名非裔美国人中进行了全基因组关联研究(GWAS)。我们复制了先前在白种人中与 CHD 或其危险因素相关的 17 个位点。对于这五个区域(CHD:CDKN2A/CDKN2B;HDL-C:FADS1-3、PLTP、LPL 和 ABCA1),我们可以利用非裔美国人独特的连锁不平衡(LD)模式来确定与表型相关性更强的 DNA 多态性,而不是先前在白种人群中报告的索引 SNP。我们还开发了一种用于混合人群关联测试的新方法,该方法利用等位基因和局部祖先变异。使用这种方法,我们发现了几个仅使用基本等位基因和全局祖先信息可能会错过的位点。我们的结论表明,没有主要的位点可以独特地解释非裔美国人中 CHD 的高患病率。我们的项目开发了资源和方法,解决了混合和 SNP 关联问题,从而在更大的非裔美国人联盟中最大程度地提高了遗传发现的能力。

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