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Lack of Association Between Genetic Variation in 9 Innate Immunity Genes and Baseline CRP Levels
Author(s) -
Kozlowski Piotr,
Miller David T.,
Zee Robert Y. L.,
Danik Jacqueline Suk,
Chasman Daniel I.,
Lazarus Ross,
Cook Nancy R.,
Ridker Paul M.,
Kwiatkowski David J.
Publication year - 2006
Publication title -
annals of human genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.537
H-Index - 77
eISSN - 1469-1809
pISSN - 0003-4800
DOI - 10.1111/j.1469-1809.2005.00256.x
Subject(s) - innate immune system , biology , baseline (sea) , immunity , gene , genetics , genetic variation , immunology , immune system , fishery
Summary It is well‐known that baseline levels of C‐reactive protein (CRP) are an independent cardiovascular risk factor. We hypothesized that genetic variation with significant influence on CRP levels might be found in genes of the innate immunity system. We performed a candidate gene association study examining common single nucleotide polymorphisms in 9 innate immunity genes ( CARD15 , IRAK1 , IRAK4 , LBP , LY86 , MEFV , TLR2 , TLR4 and NFKB1 ) in relation to CRP levels. Seven hundred and seventeen subjects from the Women's Health Study population were studied: 359 and 358 samples with extremely low (<0.2 mg/liter) and high (>5 mg/liter) CRP levels, respectively. SNPs were identified from publicly available resequencing data, using a minor allele frequency threshold of >5% and a linkage disequilibrium (LD)‐based strategy (r 2 > 0.8) to select 63 LD‐independent markers. One non‐synonymous SNP in TLR4 and two non‐synonymous SNPs in CARD15 , previously associated with atherosclerosis and Crohn's disease, respectively, were also studied. Univariate, haplotype and gene‐gene interaction analyses all indicated no significant association with CRP levels. Although this work excludes a significant association of common SNPs in these nine genes with CRP levels, it is possible that rarer alleles in these genes, or variation in other innate immunity genes, could be associated with variation in CRP.