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PMID: 17092990 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Odds ratio based multifactor-dimensionality reduction method for detecting gene-gene interactions.

Bioinformatics (Oxford, England) ·Vol. 23 ·No. 1 ·2007-01-01 ·Pages 71-6

Chung Y, Lee SY, Elston RC, Park T

Abstract

The identification and characterization of genes that increase the susceptibility to common complex multifactorial diseases is a challenging task in genetic association studies. The multifactor dimensionality reduction (MDR) method has been proposed and implemented by Ritchie et al. (2001) to identify the combinations of multilocus genotypes and discrete environmental factors that are associated with a particular disease. However, the original MDR method classifies the combination of multilocus genotypes into high-risk and low-risk groups in an ad hoc manner based on a simple comparison of the ratios of the number of cases and controls. Hence, the MDR approach is prone to false positive and negative errors when the ratio of the number of cases and controls in a combination of genotypes is similar to that in the entire data, or when both the number of cases and controls is small. Hence, we propose the odds ratio based multifactor dimensionality reduction (OR MDR) method that uses the odds ratio as a new quantitative measure of disease risk. While the original MDR method provides a simple binary measure of risk, the OR MDR method provides not only the odds ratio as a quantitative measure of risk but also the ordering of the multilocus combinations from the highest risk to lowest risk groups. Furthermore, the OR MDR method provides a confidence interval for the odds ratio for each multilocus combination, which is extremely informative in judging its importance as a risk factor. The proposed OR MDR method is illustrated using the dataset obtained from the CDC Chronic Fatigue Syndrome Research Group. The program written in R is available.

MeSH Terms
Fatigue Syndrome, Chronic/genetics Genetic Variation Humans Membrane Transport Proteins/genetics Models, Genetic Models, Statistical Odds Ratio Polymorphism, Genetic Protein Interaction Mapping/methods Risk Assessment Transcription Factors/analysis,genetics
Chemicals
Membrane Transport Proteins Transcription Factors
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Chung Yujin
Department of Statistics, Seoul National University San 56-1 Shillim-Dong, Kwanak-Gu, Seoul 151-747, Korea.
Lee Seung Yeoun
Elston Robert C
Park Taesung
Article Info
Journal
Bioinformatics (Oxford, England)
Abbr.
Bioinformatics
ISSN
1367-4811
Published
2007-01-01
Epub
2006-00-08
Pages
71-6
Language
English
Region
England
NLM ID
9808944
Subset
IM
Grants
NIGMS NIH HHS · GM-28356 · United States
PHS HHS · P30CAD43703 · United States
NCRR NIH HHS · RR03655 · United States
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