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Empirical Hierarchical Bayes Approach to Gene-Environment Interactions: Development and Application to Genome-Wide Association Studies of Lung Cancer in TRICL
ISSN
0741-0395
Date Issued
2013
Author(s)
Viktorova, Elena
Amos, Christopher I.
Brennan, P. C.
Fehringer, Gord
Gaborieau, Valerie
Han, Younghun
Heinrich, Joachim
Chang-Claude, Jenny
Hung, Rayjean J.
Müller-Nurasyid, Martina
Risch, Angela
Lewinger, Juan Pablo
Thomas, Duncan C.
DOI
10.1002/gepi.21741
Abstract
The analysis of gene-environment (G x E) interactions remains one of the greatest challenges in the postgenome-wide association studies (GWASs) era. Recent methods constitute a compromise between the robust but underpowered case-control and powerful case-only methods. Inferences of the latter are biased when the assumption of gene-environment (G-E) independence in controls fails. We propose a novel empirical hierarchical Bayes approach to G x E interaction (EHB-GE), which benefits from greater rank power while accounting for population-based G-E correlation. Building on Lewinger et al.'s ([2007] Genet Epidemiol 31:871-882) hierarchical Bayes prioritization approach, the method first obtains posterior G-E correlation estimates in controls for each marker, borrowing strength from G-E information across the genome. These posterior estimates are then subtracted from the corresponding case-only G x E estimates. We compared EHB-GE with rival methods using simulation. EHB-GE has similar or greater rank power to detect G x E interactions in the presence of large numbers of G-E correlations with weak to strong effects or only a low number of such correlations with large effect. When there are no or only a few weak G-E correlations, Murcray et al.'s method ([2009] Am J Epidemiol 169:219-226) identifies markers with low G x E interaction effects better. We applied EHB-GE and competing methods to four lung cancer case-control GWAS from the Interdisciplinary Research in Cancer of the Lung/International Lung Cancer Consortium with smoking as environmental factor. A number of genes worth investigating were identified by the EHB-GE approach.