Many common complex traits are believed to be a result of the combined effect of genes, environmental factors and their interactions. Understanding the relationship between genetic polymorphisms and environmental exposures can help to identify high risk subgroups in the population and provide a better understanding of pathway mechanisms for complex diseases. However, most investigators conducting a search for new genes in a genome-wide association study (GWAS) do not consider gene- environment (GxE) interactions. This is in part due to a current lack of efficient statistical methods and software designed to detect interactions in high-volume genetic data. In this project, we will develop new and powerful methods for the detection of genes involved in a GxE interaction, including efficient screening techniques and Bayesian methods. These methods will be applicable to both disease (e.g. cancer, asthma) and quantitative (e.g. cholesterol, lung function) outcomes, with forms applicable to case- control and case-parent trio designs. We will also develop approaches for the detection GxE interactions using GWA data from a consortium setting. In both the single-study and consortium settings, we will establish that these methods provide improved power for finding interactions relative to standard tests, while also controlling the false positive rate. We will also develop new user-friendly software for the analysis of GxE interactions in a GWAS, and will freely distribute these programs via our website.

Public Health Relevance

Gene-environment (GxE) interactions are important contributors to the etiology of complex traits such as cancer, heart disease, and asthma. We will develop new statistical methods and freely-distributed software for efficiently detecting GxE interactions in a genome-wide association (GWA) study, a consortium of GWA studies, and in post-GWAS investigations of a candidate gene or region.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21HL115606-02
Application #
8435364
Study Section
Biomedical Computing and Health Informatics Study Section (BCHI)
Program Officer
Jaquish, Cashell E
Project Start
2012-03-01
Project End
2015-02-28
Budget Start
2013-03-01
Budget End
2014-02-28
Support Year
2
Fiscal Year
2013
Total Cost
$156,128
Indirect Cost
$60,928
Name
University of Southern California
Department
Public Health & Prev Medicine
Type
Schools of Medicine
DUNS #
072933393
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
Garcia-Albeniz, Xabier; Rudolph, Anja; Hutter, Carolyn et al. (2016) CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk. Br J Cancer 114:221-9
Su, Yu-Chen; Gauderman, William James; Berhane, Kiros et al. (2016) Adaptive Set-Based Methods for Association Testing. Genet Epidemiol 40:113-22
Zhang, Pingye; Lewinger, Juan Pablo; Conti, David et al. (2016) Detecting Gene-Environment Interactions for a Quantitative Trait in a Genome-Wide Association Study. Genet Epidemiol 40:394-403
Myers, Rachel A; Scott, Nicole M; Gauderman, W James et al. (2014) Genome-wide interaction studies reveal sex-specific asthma risk alleles. Hum Mol Genet 23:5251-9
Gao, Xiaoyi; Gauderman, W James; Liu, Yutao et al. (2013) A genome-wide association study of central corneal thickness in Latinos. Invest Ophthalmol Vis Sci 54:2435-43
Quintana, M A; Conti, D V (2013) Integrative variable selection via Bayesian model uncertainty. Stat Med 32:4938-53
Gauderman, W James; Zhang, Pingye; Morrison, John L et al. (2013) Finding novel genes by testing G × E interactions in a genome-wide association study. Genet Epidemiol 37:603-13
Quintana, Melanie A; Schumacher, Fredrick R; Casey, Graham et al. (2012) Incorporating prior biologic information for high-dimensional rare variant association studies. Hum Hered 74:184-95