Article
Candidate gene association analysis for a quantitative trait, using parent-offspring trios
Article first published online: 18 NOV 2003
DOI: 10.1002/gepi.10262
© 2003 Wiley-Liss, Inc.
Additional Information
How to Cite
Gauderman, W. J. (2003), Candidate gene association analysis for a quantitative trait, using parent-offspring trios. Genet. Epidemiol., 25: 327–338. doi: 10.1002/gepi.10262
Publication History
- Issue published online: 18 NOV 2003
- Article first published online: 18 NOV 2003
- Manuscript Accepted: 28 APR 2003
- Manuscript Received: 24 FEB 2003
Funded by
- NIH. Grant Numbers: ES10421, 5P30-ES07048
- Abstract
- References
- Cited By
Keywords:
- quantitative TDT;
- sample size;
- gene-environment interaction
Abstract
With the increasing availability of genetic data, many studies of quantitative traits focus on hypotheses related to candidate genes, and also gene-environment (G×E) and gene-gene (G×G) interactions. In a population-based sample, estimates and tests of candidate gene effects can be biased by ethnic confounding, also known as population stratification bias. This paper demonstrates that even a modest degree of ethnic confounding can lead to unacceptably high type I error rates for tests of genetic effects. The parent-offspring trio design is reviewed, and several forms of the quantitative transmission disequilibrium test (QTDT) are summarized. A variation of the QTDT (QTDTM) is described that is based on a linear regression model with multiple intercepts, one per parental mating type. This and other models are expanded to allow testing of G×E and G×G interactions. A method for computing required sample sizes using direct computations is described. Sample size requirements for tests of genetic main effects and G×E and G×G interactions are compared across various QTDT approaches to infer their efficiencies relative to one another. The QTDTM is found to meet or exceed the efficiency of other QTDT approaches. For example, the QTDTM is approximately 3% more efficient than the QTDT of Rabinowitz ([1997] Hum. Hered. 47:342–350) for testing a genetic main effect, but can be as much as twice as efficient for testing G×E interaction, and three times more efficient for testing G×G interaction. Genet Epidemiol 25:327–338, 2003. © 2003 Wiley-Liss, Inc.

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