Mazo Lopera Mauricio A, Coombes Brandon J, de Andrade Mariza
School of Statistics, National University of Colombia, Medellín, Antioquia 050022, Colombia.
Departament of Health Sciences Research, Mayo Clinic, Rochester, MN 55905, USA.
Int J Environ Res Public Health. 2017 Sep 27;14(10):1134. doi: 10.3390/ijerph14101134.
Gene-environment (GE) interaction has important implications in the etiology of complex diseases that are caused by a combination of genetic factors and environment variables. Several authors have developed GE analysis in the context of independent subjects or longitudinal data using a gene-set. In this paper, we propose to analyze GE interaction for discrete and continuous phenotypes in family studies by incorporating the relatedness among the relatives for each family into a generalized linear mixed model (GLMM) and by using a gene-based variance component test. In addition, we deal with collinearity problems arising from linkage disequilibrium among single nucleotide polymorphisms (SNPs) by considering their coefficients as random effects under the null model estimation. We show that the best linear unbiased predictor (BLUP) of such random effects in the GLMM is equivalent to the ridge regression estimator. This equivalence provides a simple method to estimate the ridge penalty parameter in comparison to other computationally-demanding estimation approaches based on cross-validation schemes. We evaluated the proposed test using simulation studies and applied it to real data from the Baependi Heart Study consisting of 76 families. Using our approach, we identified an interaction between BMI and the Peroxisome Proliferator Activated Receptor Gamma () gene associated with diabetes.
基因-环境(GE)相互作用在由遗传因素和环境变量共同导致的复杂疾病病因学中具有重要意义。几位作者已在独立个体或使用基因集的纵向数据背景下开展了GE分析。在本文中,我们提议通过将每个家庭中亲属间的相关性纳入广义线性混合模型(GLMM)并使用基于基因的方差成分检验,来分析家庭研究中离散和连续表型的GE相互作用。此外,我们通过在无效模型估计下将单核苷酸多态性(SNP)之间连锁不平衡产生的共线性问题视为随机效应来处理。我们表明,GLMM中此类随机效应的最佳线性无偏预测器(BLUP)等同于岭回归估计器。与其他基于交叉验证方案的计算要求较高的估计方法相比,这种等效性提供了一种估计岭惩罚参数的简单方法。我们通过模拟研究评估了所提出的检验,并将其应用于来自包含76个家庭的Baependi心脏研究的真实数据。使用我们的方法,我们识别出了体重指数(BMI)与过氧化物酶体增殖物激活受体γ(PPARγ)基因之间与糖尿病相关的相互作用。