Gene x environment interaction (GxE) in complex human phenotypes is likely to be common, important and difficult to detect. In particular, for the understanding of behavioral and psychiatric phenotypes, approaches are needed that bring together multiple levels of genetic, biological, psychological and social factors, allowing for the interaction and correlation of these factors. However, statistical tests for interaction are prone to both false positive (as the presence of statistical interaction is dependent on how the main effects are defined) and false negative results (as tests for interaction suffer from low power). Furthermore, in the context of large scale association analysis (in which multiple testing is already a critical issue) incorporation of GxE, if lacking the appropriate statistical rigor, could potentially only exacerbate the considerable set of existing problems. This application aims to develop and evaluate new methodology with specific emphasis on robustness to nonlinear effects; to extend current methods to fit causal models to multiple genes and multiple environments; to develop and evaluate a framework for incorporating GxE in large-scale association studies in a way that refines provisional positive associations rather than increasing the multiple testing burden; to perform an exploratory simulation study within a developmental framework to investigate the likelihood and impact of nonlinear effects; to create freely-distributed software implementations. Expanding on preliminary studies, the objective is to develop and implement a maximum likelihood approach to provide a general framework for testing for GxE in families and unrelated individuals, for dichotomous and continuous traits, for allelic, genotypic or haplotypic association. Simulation studies (using both standard approaches based on asymptotic theory as well as a dynamic, nonlinear developmental approach) have been designed that will assess the performance of the methods across a broad range of genetic models. ? ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Small Research Grants (R03)
Project #
5R03MH073806-02
Application #
7281178
Study Section
Behavioral Genetics and Epidemiology Study Section (BGES)
Program Officer
Yao, Yin Y
Project Start
2006-09-01
Project End
2008-08-31
Budget Start
2007-09-01
Budget End
2008-08-31
Support Year
2
Fiscal Year
2007
Total Cost
$84,963
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
Purcell, Shaun; Neale, Benjamin; Todd-Brown, Kathe et al. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81:559-75