TY - JOUR
T1 - Powerful multilocus tests of genetic association in the presence of gene-gene and gene-environment interactions
AU - Chatterjee, Nilanjan
AU - Kalaylioglu, Zeynep
AU - Moslehi, Roxana
AU - Peters, Ulrike
AU - Wacholder, Sholom
N1 - Funding Information:
We thank Drs. Glen Satten and Alice Whittemore and two anonymous reviewers for their positive comments on an earlier version of this article. Resequencing of the GPX3 and GPX4 genes and genotyping assays for the NAT2 gene were performed at the Core Genotyping Facility at the NCI Advanced Technology Center, in Gaithersburg, MD. 39 This research was supported by the Intramural Program of the National Institutes of Health.
PY - 2006/12
Y1 - 2006/12
N2 - In modern genetic epidemiology studies, the association between the disease and a genomic region, such as a candidate gene, is often investigated using multiple SNPs. We propose a multilocus test of genetic association that can account for genetic effects that might be modified by variants in other genes or by environmental factors. We consider use of the venerable and parsimonious Tukey's 1-degree-of-freedom model of interaction, which is natural when individual SNPs within a gene are associated with disease through a common biological mechanism; in contrast, many standard regression models are designed as if each SNP has unique functional significance. On the basis of Tukey's model, we propose a novel but computationally simple generalized test of association that can simultaneously capture both the main effects of the variants within a genomic region and their interactions with the variants in another region or with an environmental exposure. We compared performance of our method with that of two standard tests of association, one ignoring gene-gene/gene-environment interactions and the other based on a saturated model of interactions. We demonstrate major power advantages of our method both in analysis of data from a case-control study of the association between colorectal adenoma and DNA variants in the NAT2 genomic region, which are well known to be related to a common biological phenotype, and under different models of gene-gene interactions with use of simulated data.
AB - In modern genetic epidemiology studies, the association between the disease and a genomic region, such as a candidate gene, is often investigated using multiple SNPs. We propose a multilocus test of genetic association that can account for genetic effects that might be modified by variants in other genes or by environmental factors. We consider use of the venerable and parsimonious Tukey's 1-degree-of-freedom model of interaction, which is natural when individual SNPs within a gene are associated with disease through a common biological mechanism; in contrast, many standard regression models are designed as if each SNP has unique functional significance. On the basis of Tukey's model, we propose a novel but computationally simple generalized test of association that can simultaneously capture both the main effects of the variants within a genomic region and their interactions with the variants in another region or with an environmental exposure. We compared performance of our method with that of two standard tests of association, one ignoring gene-gene/gene-environment interactions and the other based on a saturated model of interactions. We demonstrate major power advantages of our method both in analysis of data from a case-control study of the association between colorectal adenoma and DNA variants in the NAT2 genomic region, which are well known to be related to a common biological phenotype, and under different models of gene-gene interactions with use of simulated data.
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U2 - 10.1086/509704
DO - 10.1086/509704
M3 - Article
C2 - 17186459
AN - SCOPUS:33845284533
SN - 0002-9297
VL - 79
SP - 1002
EP - 1016
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
IS - 6
ER -