Abstract

Identifying gene-environment (G x E) interactions has become a crucial issue in the past decades. Different methods have been proposed to test for G x E interactions in the framework of linkage or association testing. However, their respective performances have rarely been compared. Using Genetic Analysis Workshop 15 simulated data, we compared the power of four methods: one based on affected sib pairs that tests for linkage and interaction (the mean interaction test) and three methods that test for association and/or interaction: a case-control test, a case-only test, and a log-linear approach based on case-parent trios. Results show that for the particular model of interaction between tobacco use and Locus B simulated here, the mean interaction test has poor power to detect either the genetic effect or the interaction. The association studies, i.e., the log-linear-modeling approach and the case-control method, are more powerful to detect the genetic effect (power of 78% and 95%, respectively) and taking into account interaction moderately increases the power (increase of 9% and 3%, respectively). The case-only design exhibits a 95% power to detect G x E interaction but the type I error rate is increased.

Highlights

  • Gene-environment (G × E) interactions are likely to play an important role in multifactorial diseases

  • We found that mean interaction test (MIT) has almost no power to detect linkage even when accounting for G × E interaction

  • With the log-linear model, the power to detect the gene effect is 78% and is increased to 87% when accounting for G × E interaction

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Summary

Introduction

Gene-environment (G × E) interactions are likely to play an important role in multifactorial diseases. On the other hand, taking it into account may either enhance or reduce the power to detect genetic susceptibility factors, depending on the parameters inherent to the model underlying disease susceptibility [2,3]. With this in mind, many statistical methods have been developed in the past decades, either to directly investigate G × E interaction or to enhance detection of genetic factors by taking (page number not for citation purposes). BMC Proceedings 2007, 1(Suppl 1):S74 http://www.biomedcentral.com/1753-6561/1/S1/S74 into account exposure status. They can be classified according to the design followed, the kind of data used, and the hypothesis tested [1,4]

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