ArticleStatistics in medicine2019
A general approach to detect gene (G)-environment (E) additive interaction leveraging G-E independence in case-control studies.
Article in Statistics in medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Statistical Methods for Chemical Mixtures: A Roadmap for Practitioners Using Simulation Studies and a Sample Data Analysis in the PROTECT Cohort.Environmental health perspectives · 2025Article
- A Robust Test for Additive Gene-Environment Interaction Under the Trend Effect of Genotype Using an Empirical Bayes-Type Shrinkage Estimator.American journal of epidemiology · 2021Article
- A Likelihood Ratio Test for Gene-Environment Interaction Based on the Trend Effect of Genotype Under an Additive Risk Model Using the Gene-Environment Independence Assumption.American journal of epidemiology · 2021Article
- Robust Tests for Additive Gene-Environment Interaction in Case-Control Studies Using Gene-Environment Independence.American journal of epidemiology · 2018Article
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Authors and funding
4 authors.
Funding
Abstract
It is increasingly of interest in statistical genetics to test for the presence of an additive interaction between genetic (G) and environmental (E) risk factors. In case-control studies involving a rare disease, a statistical test of no additive G×E interaction typically entails a test of no relative excess risk due to interaction (RERI). It has been shown that a likelihood ratio test of a null RERI incorporating the G-E independence assumption (RERI-LRT) outperforms the standard approach. The RERI-LRT relies on correct specification of a logistic model for the binary outcome, as a function of G, E, and auxiliary covariates. However, when at least one exposure is not categorical or auxiliary covariates are present, nonparametric estimation may not be feasible, while parametric logistic regression will a priori rule out the null hypothesis of no additive interaction in most practical situations, inflating type I error rate. In this paper, we present a general approach to test for G × E additive interaction exploiting G-E independence. Unlike the RERI-LRT, it allows the regression model for the binary outcome to remain unrestricted, and nonetheless still allows for covariate adjustment in order to ensure the G-E independence assumption or to rule out residual confounding. The methods are illustrated through extensive simulation studies and an ovarian cancer study.
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