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Logic Regression for Analysis of the Association between Genetic Variation in the Renin-Angiotensin System and Myocardial Infarction or Stroke
Author(s) -
Charles Kooperberg,
Josh Bis,
Kristin D. Marciante,
Susan R. Heckbert,
Thomas Lumley,
Bruce M. Psaty
Publication year - 2006
Publication title -
american journal of epidemiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.33
H-Index - 256
eISSN - 1476-6256
pISSN - 0002-9262
DOI - 10.1093/aje/kwk006
Subject(s) - single nucleotide polymorphism , snp , myocardial infarction , stroke (engine) , genotype , genetic association , haplotype , observational study , medicine , genetic variants , genetic variation , renin–angiotensin system , bioinformatics , biology , genetics , gene , blood pressure , mechanical engineering , engineering
Recent developments in genetic sequencing technology now make it possible to genotype large numbers of single nucleotide polymorphisms (SNPs) in large samples. Many association studies using SNP data are now being carried out. Typically, these observational studies establish whether certain haplotypes or individual SNPs are associated with a health outcome. Few methods exist for finding interaction effects among multiple SNPs or between SNPs and environmental factors. In this paper, the authors describe logic regression, an exploratory method with which to identify interactions for further research. They illustrate this method using data from a US case-control study of myocardial infarction and stroke (1995-1999) carried out among 1,614 persons in Washington State who were genotyped for 32 SNPs on five genes in the renin-angiotensin system.

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