Shriner Daniel, Bentley Amy R, Doumatey Ayo P, Zhou Jie, Chen Guanjie, Rotimi Charles N, Adeyemo Adebowale A
Center for Research on Genomics and Global Health, National Human Genome Research Institute, Bethesda, Maryland, USA.
Genet Epidemiol. 2025 Jun;49(4):e70009. doi: 10.1002/gepi.70009.
Conventional genome-wide association studies (GWAS) are designed to assess the effect of a genetic locus on phenotypic mean by genotype. Such loci explain a proportion of phenotypic variance known as narrow-sense heritability. In contrast, variance quantitative trait loci (vQTL) are associated with the phenotypic variance by genotype. These loci explain an additional proportion of phenotypic variance and contribute to broad-sense heritability but not to narrow-sense heritability. Here, a genome-wide vQTL analysis in 22,805 African Americans yielded eight loci for body mass index (BMI). Of these loci, three were replicated in 6002 sub-Saharan Africans. No locus reached genome-wide significance using the standard additive model. Furthermore, no locus showed evidence for natural selection, haplotype effects, or gene × sex or gene × study interactions. Two loci showed evidence for an effect of locus-specific ancestry resulting from admixture and for a gene × gene interaction. One locus showed evidence for interaction with diastolic blood pressure, consistent with this vQTL capturing an unmodeled gene × covariate interaction. These analyses demonstrate that relevant BMI loci can be detected by evaluating vQTL and that these loci contribute to the underexplored broad-sense heritability for this trait.
传统的全基因组关联研究(GWAS)旨在通过基因型评估基因座对表型均值的影响。此类基因座解释了一部分表型方差,即狭义遗传力。相比之下,方差数量性状基因座(vQTL)通过基因型与表型方差相关联。这些基因座解释了额外的一部分表型方差,并对广义遗传力有贡献,但对狭义遗传力没有贡献。在此,对22805名非裔美国人进行的全基因组vQTL分析产生了8个与体重指数(BMI)相关的基因座。在这些基因座中,有3个在6002名撒哈拉以南非洲人中得到了重复验证。使用标准加性模型时,没有一个基因座达到全基因组显著性。此外,没有一个基因座显示出自然选择、单倍型效应或基因×性别或基因×研究相互作用的证据。两个基因座显示出因混合而产生的基因座特异性祖先效应以及基因×基因相互作用的证据。一个基因座显示出与舒张压相互作用的证据,这与该vQTL捕捉到未建模的基因×协变量相互作用一致。这些分析表明,通过评估vQTL可以检测到相关的BMI基因座,并且这些基因座对该性状尚未充分探索的广义遗传力有贡献。