Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; Population Health Services, Geisinger Health, Danville, PA 17822, USA.
Am J Hum Genet. 2021 Apr 1;108(4):564-582. doi: 10.1016/j.ajhg.2021.02.011. Epub 2021 Mar 12.
Although many loci have been associated with height in European ancestry populations, very few have been identified in African ancestry individuals. Furthermore, many of the known loci have yet to be generalized to and fine-mapped within a large-scale African ancestry sample. We performed sex-combined and sex-stratified meta-analyses in up to 52,764 individuals with height and genome-wide genotyping data from the African Ancestry Anthropometry Genetics Consortium (AAAGC). We additionally combined our African ancestry meta-analysis results with published European genome-wide association study (GWAS) data. In the African ancestry analyses, we identified three novel loci (SLC4A3, NCOA2, ECD/FAM149B1) in sex-combined results and two loci (CRB1, KLF6) in women only. In the African plus European sex-combined GWAS, we identified an additional three novel loci (RCCD1, G6PC3, CEP95) which were equally driven by AAAGC and European results. Among 39 genome-wide significant signals at known loci, conditioning index SNPs from European studies identified 20 secondary signals. Two of the 20 new secondary signals and none of the 8 novel loci had minor allele frequencies (MAF) < 5%. Of 802 known European height signals, 643 displayed directionally consistent associations with height, of which 205 were nominally significant (p < 0.05) in the African ancestry sex-combined sample. Furthermore, 148 of 241 loci contained ≤20 variants in the credible sets that jointly account for 99% of the posterior probability of driving the associations. In summary, trans-ethnic meta-analyses revealed novel signals and further improved fine-mapping of putative causal variants in loci shared between African and European ancestry populations.
尽管许多基因座与欧洲血统人群的身高相关,但在非洲血统个体中仅发现了极少数基因座。此外,许多已知的基因座尚未在大规模的非洲血统样本中进行概括和精细映射。我们对来自非洲祖先人体测量遗传学联盟(AAAGC)的身高和全基因组基因分型数据的最多 52764 个人进行了联合和性别分层的荟萃分析。我们还将我们的非洲祖先荟萃分析结果与已发表的欧洲全基因组关联研究(GWAS)数据相结合。在非洲祖先分析中,我们在联合性别分析中确定了三个新的基因座(SLC4A3、NCOA2、ECD/FAM149B1),在女性中仅确定了两个基因座(CRB1、KLF6)。在非洲加欧洲联合性别 GWAS 中,我们确定了另外三个新的基因座(RCCD1、G6PC3、CEP95),这些基因座同样由 AAAGC 和欧洲结果驱动。在已知基因座的 39 个全基因组显着信号中,欧洲研究的条件指数 SNP 确定了 20 个次要信号。20 个新的次要信号中的两个和 8 个新基因座中的没有一个具有小于 5%的次要等位基因频率(MAF)。在 802 个已知的欧洲身高信号中,有 643 个与身高呈定向一致的关联,其中 205 个在非洲祖先联合性别样本中具有统计学意义(p<0.05)。此外,241 个基因座中有 148 个包含在联合解释 99%关联后验概率的可信集内的变体数量≤20,这些可信集共同解释了 99%的关联后验概率。总之,跨种族荟萃分析揭示了新的信号,并进一步改善了非洲和欧洲血统人群共享基因座中潜在因果变异的精细映射。