Department of Biostatistics, University of Washington, Seattle, Washington.
Institute for Public Health Genetics, University of Washington, Seattle, Washington.
J Am Soc Nephrol. 2022 Jan;33(1):77-87. doi: 10.1681/ASN.2021050617. Epub 2021 Oct 20.
Admixture mapping is a powerful approach for gene mapping of complex traits that leverages the diverse genetic ancestry in populations with recent admixture, such as Hispanic or Latino individuals in the United States. These individuals have an increased risk of CKD.
We performed genome-wide admixture mapping for both CKD and eGFR in a sample of 12,601 participants from the Hispanic Community Health Study/Study of Latinos, with validation in a sample of 8191 Black participants from the Women's Health Initiative (WHI). We also compared the findings with those from a conventional genome-wide association study.
Three novel ancestry-of-origin loci were identified on chromosomes 2, 14, and 15 for CKD and eGFR. The chromosome 2 locus comprises two European ancestry regions encompassing the and genes, with European ancestry at this locus associated with increased CKD risk. The chromosome 14 locus, found within the imprinted domain, was associated with lower eGFR and driven by European ancestry. The eGFR-associated locus on chromosome 15 included intronic variants of and was within an African-specific genomic region associated with higher eGFR. The genome-wide association study failed to identify significant associations in these regions. We validated the chromosome 14 and 15 loci associated with eGFR in the WHI Black participants.
This study provides evidence of shared ancestry-specific genomic regions influencing eGFR in Hispanic or Latino individuals and Black individuals and illustrates the potential for leveraging genetic ancestry in recently admixed populations for the discovery of novel candidate loci for kidney phenotypes.
混合映射是一种强大的方法,可用于对具有近期混合遗传背景的人群(如美国的西班牙裔或拉丁裔个体)的复杂特征进行基因映射,这些人群患有 CKD 的风险增加。
我们在 12601 名来自西班牙裔社区健康研究/拉丁裔研究的参与者样本中对 CKD 和 eGFR 进行了全基因组混合映射,并在 8191 名来自妇女健康倡议(WHI)的黑人参与者样本中进行了验证。我们还将这些发现与传统的全基因组关联研究进行了比较。
在 CKD 和 eGFR 方面,我们在染色体 2、14 和 15 上确定了三个新的起源祖先位点。染色体 2 位点包含两个欧洲祖先区域,包含 和 基因,该位点的欧洲祖先与增加的 CKD 风险相关。在染色体 14 位点上,在印迹域内发现,与较低的 eGFR 相关,并受欧洲祖先的驱动。与染色体 15 上的 eGFR 相关的位点包括 和的内含子变体,位于与较高 eGFR 相关的非洲特异性基因组区域内。全基因组关联研究未能在这些区域中确定显著关联。我们在 WHI 黑人参与者中验证了与 eGFR 相关的染色体 14 和 15 位点。
这项研究提供了证据表明,共享的祖先特异性基因组区域影响了西班牙裔或拉丁裔个体和黑人个体的 eGFR,并说明了在最近混合的人群中利用遗传背景发现肾脏表型的新候选基因座的潜力。