Gene-environment Interactions in Genome-wide Association Studies: a Comparative Study of Tests Applied to Empirical Studies of Type 2 Diabetes
Overview
Authors
Affiliations
The question of which statistical approach is the most effective for investigating gene-environment (G-E) interactions in the context of genome-wide association studies (GWAS) remains unresolved. By using 2 case-control GWAS (the Nurses' Health Study, 1976-2006, and the Health Professionals Follow-up Study, 1986-2006) of type 2 diabetes, the authors compared 5 tests for interactions: standard logistic regression-based case-control; case-only; semiparametric maximum-likelihood estimation of an empirical-Bayes shrinkage estimator; and 2-stage tests. The authors also compared 2 joint tests of genetic main effects and G-E interaction. Elevated body mass index was the exposure of interest and was modeled as a binary trait to avoid an inflated type I error rate that the authors observed when the main effect of continuous body mass index was misspecified. Although both the case-only and the semiparametric maximum-likelihood estimation approaches assume that the tested markers are independent of exposure in the general population, the authors did not observe any evidence of inflated type I error for these tests in their studies with 2,199 cases and 3,044 controls. Both joint tests detected markers with known marginal effects. Loci with the most significant G-E interactions using the standard, empirical-Bayes, and 2-stage tests were strongly correlated with the exposure among controls. Study findings suggest that methods exploiting G-E independence can be efficient and valid options for investigating G-E interactions in GWAS.
Characterizing the genetic architecture of drug response using gene-context interaction methods.
Sadowski M, Thompson M, Mefford J, Haldar T, Oni-Orisan A, Border R Cell Genom. 2024; 4(12):100722.
PMID: 39637863 PMC: 11701255. DOI: 10.1016/j.xgen.2024.100722.
Genetics of glucose homeostasis in pregnancy and postpartum.
Lowe Jr W, Kuang A, Hayes M, Hivert M, Scholtens D Diabetologia. 2024; 67(12):2726-2739.
PMID: 39180581 DOI: 10.1007/s00125-024-06256-8.
Horimoto A, Sun Q, Lash J, Daviglus M, Cai J, Haack K Circ Genom Precis Med. 2024; 17(4):e004314.
PMID: 38950085 PMC: 11394365. DOI: 10.1161/CIRCGEN.123.004314.
Wu Y, Chen W, Zhao Y, Gu M, Gao Y, Ke Y J Hum Genet. 2024; 69(7):311-319.
PMID: 38528048 DOI: 10.1038/s10038-024-01243-8.
A Varying Coefficient Model to Jointly Test Genetic and Gene-Environment Interaction Effects.
Zhou Z, Ku H, Manning S, Zhang M, Xing C Behav Genet. 2023; 53(4):374-382.
PMID: 36622576 PMC: 10277225. DOI: 10.1007/s10519-022-10131-w.