Association of Leukotriene Gene Variants and Plasma LTB4 Levels with Coronary Artery Disease in Asian Indians
Author(s) -
Jiny Nair,
Jayashree Shanker,
Prathima Arvind,
Srikarthika Jambunathan,
Vijay V. Kakkar
Publication year - 2013
Publication title -
isrn vascular medicine
Language(s) - English
Resource type - Journals
eISSN - 2090-5831
pISSN - 2090-5823
DOI - 10.1155/2013/985743
Subject(s) - coronary artery disease , single nucleotide polymorphism , quartile , leukotriene b4 , medicine , algorithm , genotype , biology , gene , mathematics , genetics , inflammation , confidence interval
Leukotrienes are potent inflammatory and lipid mediators that participate in atherosclerosis. We analyzed the association of Leukotriene gene (ALOX5, ALOX5AP, LTA4H, and LTC4S) polymorphisms and plasma Leukotriene B4 (LTB4) levels with coronary artery disease (CAD) in a representative cohort of Asian Indians. In all, 136 functional single nucleotide polymorphisms (SNPs) were selected using in silico tools. Forty-five polymorphic SNPs were ranked for predicted functional effect using FastSNP. Finally, 14 functional SNPs along with 10 SNPs identified from the literature were genotyped in 340 CAD patients and 340 controls. Plasma LTB4 levels were measured in 150 cases and 150 controls. None of the 24 SNPs showed significant association with CAD. Plasma LTB4 levels were higher in cases than in controls ( pg/mL versus pg/mL) (), with greater risk being associated with the top quartile as compared to the bottom quartile after adjusting for potential confounders (OR 8.94, 95% CI 2.56–31.95; ). Four SNPs in the LTA4H gene showed significant association with LTB4 levels () of which rs1978331 () remained significant after correction for multiple testing. LTB4 showed strong correlation with lipids (–34) only in cases. Our pilot study suggests that the association between Leukotrienes gene polymorphisms and CAD risk may be modulated through plasma LTB4 levels.
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