Abstract

BackgroundInteractions of single nucleotide polymorphisms (SNPs) and environmental factors play an important role in understanding complex diseases' pathogenesis. A growing number of SNP-environment studies have been conducted in the past decade; however, the statistical methods for evaluating SNP-environment interactions are still underdeveloped. The conventional statistical approach with a full interaction model with an additive SNP mode tests one specific interaction type, so the full interaction model approach tends to lead to false-negative findings. To increase detection accuracy, developing a statistical tool to effectively detect various SNP-environment interaction patterns is necessary.ResultsSNPxE, a SNP-environment interaction pattern identifier, tests multiple interaction patterns associated with a phenotype for each SNP-environment pair. SNPxE evaluates 27 interaction patterns for an ordinal environment factor and 18 patterns for a categorical environment factor. For detecting SNP-environment interactions, SNPxE considers three major components: (1) model structure, (2) SNP’s inheritance mode, and (3) risk direction. Among the multiple testing patterns, the best interaction pattern will be identified based on the Bayesian information criterion or the smallest p-value of the interaction. Furthermore, the risk sub-groups based on the SNPs and environmental factors can be identified. SNPxE can be applied to both numeric and binary phenotypes. For better results interpretation, a heat-table of the outcome proportions can be generated for the sub-groups of a SNP-environment pair.ConclusionsSNPxE is a valuable tool for intensively evaluate SNP-environment interactions, and the SNPxE findings can provide insights for solving the missing heritability issue. The R function of SNPxE is freely available for download at GitHub (https://github.com/LinHuiyi/SIPI).

Highlights

  • Interactions of single nucleotide polymorphisms (SNPs) and environ‐ mental factors play an important role in understanding complex diseases’ pathogen‐ esis

  • By adopting a similar concept, the objective of this study is to develop the novel "SNP-Environment Interaction Pattern Identifier (SNPxE)" approach and software (“SNPxE” R function inside the SNP Interaction Pattern Identifier (SIPI) R package) to test SNP-environment interactions associated with a phenotype by considering multiple interaction patterns

  • The p-values of the 27 patterns are in a wide range of 0.012–0.998. This example demonstrates that the selection of testing patterns plays an important role in testing SNP-environment interactions

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Summary

Introduction

Interactions of single nucleotide polymorphisms (SNPs) and environ‐ mental factors play an important role in understanding complex diseases’ pathogen‐ esis. The conventional statistical approach with a full interaction model with an additive SNP mode tests one specific interaction type, so the full inter‐ action model approach tends to lead to false-negative findings. To increase detection accuracy, developing a statistical tool to effectively detect various SNP-environment interaction patterns is necessary. It is well known that genetic factors or environmental risk factors alone are not sufficient to explain the complexity of disease causality. It has been shown that gene-environment interactions play an important role in the etiology of complex diseases [1,2,3,4,5,6]. SNPs can modify an environmental factor’s impact on complex diseases and vice versa

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