Kernel-based genetic association analysis for microbiome phenotypes identifies host genetic drivers of beta-diversity
Hongjiao LiuiD, Wodan LingiD, Xing HuaiD, Jee‐Young MooniD, Jessica S Williams-NguyeniD, Xiang ZhaniD, Anna PlantingaiD, Ni ZhaoiD, Angela Yu ZhangiD, Rob D. KnightiD, Qibin QiiD, Robert David BurkiD, Robert C. KaplaniD, Michael C. WuiD
Abstract
Understanding human genetic influences on the gut microbiota helps elucidate the mechanisms by which genetics affects health outcomes. We propose a novel approach, the covariate-adjusted kernel RV (KRV) framework, to map genetic variants associated with microbiome beta-diversity, which focuses on overall shifts in the microbiota. The proposed KRV framework improves statistical power by capturing intrinsic structure within the genetic and microbiome data while reducing the multiple-testing burden. We apply the covariate-adjusted KRV test to the Hispanic Community Health Study/Study of Latinos in a genome-wide association analysis (first gene-level, then variant-level) for microbiome beta-diversity. We have identified an immunity-related gene, IL23R, reported in previous association studies and discovered 3 other novel genes, 2 of which are involved in immune functions or autoimmune disorders. Our findings highlight the value of the KRV as a powerful microbiome GWAS approach and support an important role of immunity-related genes in shaping the gut microbiome composition.
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