Literature DB >> 25585620

Assessing gene-environment interactions for common and rare variants with binary traits using gene-trait similarity regression.

Guolin Zhao1, Rachel Marceau1, Daowen Zhang1, Jung-Ying Tzeng2.   

Abstract

Accounting for gene-environment (G×E) 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 G×E 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 G×E interactions for rare variants with binary traits. The proposed model aggregates the genetic and G×E information across markers, using genetic similarity, thus increasing the ability to detect G×E signals. The model has a random effects interpretation, which leads to robustness against main-effect misspecifications when evaluating G×E interactions. We construct score tests to examine G×E 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 G×E effect in common or rare variant studies with binary traits.
Copyright © 2015 by the Genetics Society of America.

Entities:  

Keywords:  GLMM; binary traits; gene–environment interaction; marker-set interaction analysis; rare variant association; variance-component methods

Mesh:

Year:  2015        PMID: 25585620      PMCID: PMC4349065          DOI: 10.1534/genetics.114.171686

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.402


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