» Articles » PMID: 22771729

Simultaneously Testing for Marginal Genetic Association and Gene-environment Interaction

Overview
Journal Am J Epidemiol
Specialty Public Health
Date 2012 Jul 10
PMID 22771729
Citations 28
Authors
Affiliations
Soon will be listed here.
Abstract

In this article, the authors propose to simultaneously test for marginal genetic association and gene-environment interaction to discover single nucleotide polymorphisms that may be involved in gene-environment or gene-treatment interaction. The asymptotic independence of the marginal association estimator and various interaction estimators leads to a simple and flexible way of combining the 2 tests, allowing for exploitation of gene-environment independence in estimating gene-environment interaction. The proposed test differs from the 2-df test proposed by Kraft et al. (Hum Hered. 2007;63(2):111-119) in two respects. First, for the genetic association component, it tests for marginal association, which is often the primary objective in inference, rather than the main effect in a model with gene-environment interaction. Second, the gene-environment testing component can easily exploit putative gene-environment independence using either the case-only estimator or the empirical Bayes estimator, depending on whether the goal is gene-treatment interaction in a randomized trial or gene-environment interaction in an observational study. The use of the proposed joint test is illustrated through simulations and a genetic study (1993-2005) from the Women's Health Initiative.

Citing Articles

A general kernel machine regression framework using principal component analysis for jointly testing main and interaction effects: Applications to human microbiome studies.

Koh H NAR Genom Bioinform. 2024; 6(4):lqae148.

PMID: 39534501 PMC: 11555437. DOI: 10.1093/nargab/lqae148.


A versatile, fast and unbiased method for estimation of gene-by-environment interaction effects on biobank-scale datasets.

Di Scipio M, Khan M, Mao S, Chong M, Judge C, Pathan N Nat Commun. 2023; 14(1):5196.

PMID: 37626057 PMC: 10457310. DOI: 10.1038/s41467-023-40913-7.


Probing the diabetes and colorectal cancer relationship using gene - environment interaction analyses.

Dimou N, Kim A, Flanagan O, Murphy N, Diez-Obrero V, Shcherbina A Br J Cancer. 2023; 129(3):511-520.

PMID: 37365285 PMC: 10403521. DOI: 10.1038/s41416-023-02312-z.


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.


Association of Body Mass Index With Colorectal Cancer Risk by Genome-Wide Variants.

Campbell P, Lin Y, Bien S, Figueiredo J, Harrison T, Guinter M J Natl Cancer Inst. 2020; 113(1):38-47.

PMID: 32324875 PMC: 7781451. DOI: 10.1093/jnci/djaa058.


References
1.
Murcray C, Lewinger J, Conti D, Thomas D, Gauderman W . Sample size requirements to detect gene-environment interactions in genome-wide association studies. Genet Epidemiol. 2011; 35(3):201-10. PMC: 3076801. DOI: 10.1002/gepi.20569. View

2.
Umbach D, Weinberg C . Designing and analysing case-control studies to exploit independence of genotype and exposure. Stat Med. 1997; 16(15):1731-43. DOI: 10.1002/(sici)1097-0258(19970815)16:15<1731::aid-sim595>3.0.co;2-s. View

3.
Murcray C, Lewinger J, Gauderman W . Gene-environment interaction in genome-wide association studies. Am J Epidemiol. 2008; 169(2):219-26. PMC: 2732981. DOI: 10.1093/aje/kwn353. View

4.
Kooperberg C, LeBlanc M . Increasing the power of identifying gene x gene interactions in genome-wide association studies. Genet Epidemiol. 2008; 32(3):255-63. PMC: 2955421. DOI: 10.1002/gepi.20300. View

5.
Rossouw J, Anderson G, Prentice R, LaCroix A, Kooperberg C, Stefanick M . Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results From the Women's Health Initiative randomized controlled trial. JAMA. 2002; 288(3):321-33. DOI: 10.1001/jama.288.3.321. View