Department of Psychiatry, Yale University School of Medicine, West Haven, CT 06516, USA.
Department of Biology, University of Rome Tor Vergata, Rome 00133, Italy.
Hum Mol Genet. 2021 Jul 9;30(15):1457-1467. doi: 10.1093/hmg/ddab114.
To investigate cross-ancestry genetics of complex traits, we conducted a phenome-wide analysis of loci with heterogeneous effects across African, Admixed-American, Central/South Asian, East Asian, European and Middle Eastern participants of the UK Biobank (N = 441 331). Testing 843 phenotypes, we identified 82 independent genomic regions mapping variants showing genome-wide significant (GWS) associations (P < 5 × 10-8) in the trans-ancestry meta-analysis and GWS heterogeneity among the ancestry-specific effects. These included (i) loci with GWS association in one ancestry and concordant but heterogeneous effects among the other ancestries and (ii) loci with a GWS association in one ancestry group and an experiment-wide significant discordant effect (P < 6.1 × 10-4) in at least another ancestry. Since the trans-ancestry GWS associations were mostly driven by the European ancestry sample size, we investigated the differences of the allele frequency (ΔAF) and linkage disequilibrium regulome tagging (ΔLD) between European populations and the other ancestries. Within loci with concordant effects, the degree of heterogeneity was associated with European-Middle Eastern ΔAF (P = 9.04 × 10-6) and ΔLD of European populations with respect to African, Admixed-American and Central/South Asian groups (P = 8.21 × 10-4, P = 7.17 × 10-4 and P = 2.16 × 10-3, respectively). Within loci with discordant effects, ΔAF and ΔLD of European populations with respect to African and Central/South Asian ancestries were associated with the degree of heterogeneity (ΔAF: P = 7.69 × 10-3 and P = 5.31 × 10-3, ΔLD: P = 0.016 and P = 2.65 × 10-4, respectively). Considering the traits associated with cross-ancestry heterogeneous loci, we observed enrichments for blood biomarkers (P = 5.7 × 10-35) and physical appearance (P = 1.38 × 10-4). This suggests that these specific phenotypic classes may present considerable cross-ancestry heterogeneity owing to large allele frequency and LD variation among worldwide populations.
为了研究复杂性状的跨种族遗传学,我们对英国生物库中具有跨种族异效的基因座进行了全表型分析,这些基因座的参与者包括非洲人、混合裔美国人、中/南亚人、东亚人、欧洲人和中东人(N=441331)。我们对 843 种表型进行了测试,鉴定出 82 个独立的基因组区域,这些区域的变异与跨种族荟萃分析中的全基因组显著关联(P<5×10-8),以及在特定种族效应中存在全基因组显著的异质性。这些区域包括:(i)在一个种族中具有全基因组显著关联的基因座,而在其他种族中则具有一致但异质性的效应;(ii)在一个种族群体中具有全基因组显著关联的基因座,而在至少另一个种族中则具有实验性全基因组显著不一致的效应(P<6.1×10-4)。由于跨种族的全基因组显著关联主要由欧洲血统样本量驱动,我们研究了欧洲人群与其他种族之间的等位基因频率(ΔAF)和连锁不平衡调控区标记(ΔLD)的差异。在具有一致效应的基因座中,异质性的程度与欧洲-中东 ΔAF 相关(P=9.04×10-6),以及欧洲人群相对于非洲、混合裔美国人和中/南亚人群的 ΔLD 相关(P=8.21×10-4,P=7.17×10-4,P=2.16×10-3)。在具有不一致效应的基因座中,欧洲人群相对于非洲和中/南亚祖先的 ΔAF 和 ΔLD 与异质性的程度相关(ΔAF:P=7.69×10-3 和 P=5.31×10-3,ΔLD:P=0.016 和 P=2.65×10-4)。考虑到与跨种族异质性基因座相关的性状,我们观察到血液生物标志物(P=5.7×10-35)和外貌(P=1.38×10-4)的富集。这表明,由于全世界人群中较大的等位基因频率和 LD 变异,这些特定的表型类别可能存在相当大的跨种族异质性。