Department of Human Genetics, University of Chicago, Chicago, Il 60637, USA.
J Allergy Clin Immunol. 2012 Sep;130(3):622-629.e9. doi: 10.1016/j.jaci.2012.03.045. Epub 2012 May 18.
Genetic variants that contribute to asthma susceptibility might be present at varying frequencies in different populations, which is an important consideration and advantage for performing genetic association studies in admixed populations.
We sought to identify asthma-associated loci in African American subjects.
We compared local African and European ancestry estimated from dense single nucleotide polymorphism genotype data in African American adults with asthma and nonasthmatic control subjects. Allelic tests of association were performed within the candidate regions identified, correcting for local European admixture.
We identified a significant ancestry association peak on chromosome 6q. Allelic tests for association within this region identified a single nucleotide polymorphism (rs1361549) on 6q14.1 that was associated with asthma exclusively in African American subjects with local European admixture (odds ratio, 2.2). The risk allele is common in Europe (42% in the HapMap population of Utah residents with Northern and Western European ancestry from the Centre d'Etude du Polymorphisme Humain collection) but absent in West Africa (0% in the HapMap population of Yorubans in Ibadan, Nigeria), suggesting the allele is present in African American subjects because of recent European admixture. We replicated our findings in Puerto Rican subjects and similarly found that the signal of association is largely specific to subjects who are heterozygous for African and non-African ancestry at 6q14.1. However, we found no evidence for association in European American or Puerto Rican subjects in the absence of local African ancestry, suggesting that the association with asthma at rs1361549 is due to an environmental or genetic interaction.
We identified a novel asthma-associated locus that is relevant to admixed populations with African ancestry and highlight the importance of considering local ancestry in genetic association studies of admixed populations.
导致哮喘易感性的遗传变异在不同人群中的出现频率可能不同,这对于在混合人群中进行遗传关联研究是一个重要的考虑因素和优势。
我们试图确定非裔美国人中与哮喘相关的基因座。
我们比较了来自非裔美国成年人哮喘和非哮喘对照个体的高密度单核苷酸多态性基因型数据中估计的局部非洲和欧洲血统。在确定的候选区域内进行了关联的等位基因测试,校正了局部欧洲混合。
我们在 6 号染色体上发现了一个显著的遗传关联峰。在该区域内进行的关联等位基因测试确定了 6q14.1 上的一个单核苷酸多态性(rs1361549),仅在具有局部欧洲混合的非裔美国人中与哮喘相关(优势比,2.2)。风险等位基因在欧洲很常见(42%在来自 Centre d'Etude du Polymorphisme Humain 收集的犹他州居民的北和西欧血统的 HapMap 人群中),但在西非不存在(0%在尼日利亚伊巴丹的约鲁巴人 HapMap 人群中),这表明该等位基因是由于最近的欧洲混合而存在于非裔美国人中。我们在波多黎各人中复制了我们的发现,同样发现,在 6q14.1 处具有非洲和非非洲血统杂合的个体中,关联的信号主要是特异性的。然而,我们在没有局部非洲血统的欧洲裔美国人和波多黎各人中没有发现关联的证据,这表明 rs1361549 与哮喘的关联是由于环境或遗传相互作用。
我们确定了一个与具有非洲血统的混合人群相关的新的哮喘相关基因座,并强调了在混合人群的遗传关联研究中考虑局部血统的重要性。