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Assessing Gene-Environment Interactions for Common and Rare Variants with Binary Traits Using Gene-Trait Similarity Regression

机译:使用基因-特征相似度回归评估具有双性状的常见和稀有变体的基因-环境相互作用

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摘要

Accounting for gene-environment (GXE) interactions in complex trait association studies can facilitate our understanding of genetic heterogeneity under different environmental exposures, improve the ability to discover susceptible genes that exhibit little marginal effect, provide insight into the biological mechanisms of complex diseases, help to identify high-risk subgroups in the population, and uncover hidden heritability. However, significant GXE interactions can be difficult to find. The sample sizes required for sufficient power to detect association are much larger than those needed for genetic main effects, and interactions are sensitive to misspecification of the main-effects model. These issues are exacerbated when working with binary phenotypes and rare variants, which bear less information on association. In this work, we present a similarity-based regression method for evaluating GXE interactions for rare variants with binary traits. The proposed model aggregates the genetic and GXE information across markers, using genetic similarity, thus increasing the ability to detect GXE signals. The model has a random effects interpretation, which leads to robustness against main-effect misspecifications when evaluating GXE interactions. We construct score tests to examine GXE interactions and a computationally efficient EM algorithm to estimate the nuisance variance components. Using simulations and data applications, we show that the proposed method is a flexible and powerful tool to study the GXE effect in common or rare variant studies with binary traits.
机译:解释复杂性状关联研究中的基因-环境(GXE)相互作用可以帮助我们理解不同环境暴露下的遗传异质性,提高发现几乎没有边际效应的易感基因的能力,提供对复杂疾病的生物学机制的洞察力,帮助确定人群中的高危亚群,并揭示隐藏的遗传力。但是,可能很难找到大量的GXE交互。足够的能力来检测关联所需的样本数量比遗传主要效应所需的样本量大得多,并且相互作用对主要效应模型的错误指定敏感。当使用二进制表型和稀有变体时,这些问题会更加严重,因为它们的关联信息较少。在这项工作中,我们提出了一种基于相似度的回归方法,用于评估具有二进制特征的稀有变体的GXE相互作用。提出的模型使用遗传相似性,跨标记汇总了遗传和GXE信息,从而提高了检测GXE信号的能力。该模型具有随机效应解释,可在评估GXE相互作用时抗主效应错误指定。我们构建分数测试来检查GXE交互作用,并使用计算效率高的EM算法来估计扰动方差分量。通过仿真和数据应用,我们证明了该方法是一种灵活而强大的工具,可用于研究具有二进制特征的常见或稀有变异研究中的GXE效应。

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