Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts, USA.
Boston University's and National Heart, Lung, and Blood Institute's Framingham Heart Study, Framingham, Massachusetts, USA.
Genet Epidemiol. 2021 Apr;45(3):280-292. doi: 10.1002/gepi.22369. Epub 2020 Oct 10.
Multiple methods have been proposed to aggregate genetic variants in a gene or a region and jointly test their association with a trait of interest. However, these joint tests do not provide estimates of the individual effect of each variant. Moreover, few methods have evaluated the joint association of multiple variants with DNA methylation. We propose a method based on linear mixed models to estimate the joint and individual effect of multiple genetic variants on DNA methylation leveraging genomic annotations. Our approach is flexible, can incorporate covariates and annotation features, and takes into account relatedness and linkage disequilibrium (LD). Our method had correct Type-I error and overall high power for different simulated scenarios where we varied the number and specificity of functional annotations, number of causal and total genetic variants, frequency of genetic variants, LD, and genetic variant effect. Our method outperformed the family Sequence Kernel Association Test and had more stable estimations of effects than a classical single-variant linear mixed-effect model. Applied genome-wide to the Framingham Heart Study data, our method identified 921 DNA methylation sites influenced by at least one rare or low-frequency genetic variant located within 50 kilobases (kb) of the DNA methylation site.
已经提出了多种方法来聚集基因或区域中的遗传变异,并联合检验它们与感兴趣性状的关联。然而,这些联合检验并没有提供每个变异个体效应的估计。此外,很少有方法评估多个变异与 DNA 甲基化的联合关联。我们提出了一种基于线性混合模型的方法,利用基因组注释来估计多个遗传变异对 DNA 甲基化的联合和个体效应。我们的方法灵活,可以包含协变量和注释特征,并考虑到相关性和连锁不平衡(LD)。在不同的模拟场景中,我们改变了功能注释的数量和特异性、因果和总遗传变异的数量、遗传变异的频率、LD 和遗传变异效应,我们的方法具有正确的Ⅰ型错误和总体高功效。将我们的方法应用于弗雷明汉心脏研究的数据,我们鉴定出了 921 个受至少一个罕见或低频遗传变异影响的 DNA 甲基化位点,这些变异位于 DNA 甲基化位点 50 千碱基(kb)内。