Lack of association between common genetic variation in endothelial lipase (LIPG) and the risk for CAD and DVT

Menno Vergeer, Danny M. Cohn, S. Matthijs Boekholdt, Manjinder S. Sandhu, Hester M. Prins, Sally L. Ricketts, Nicholas J. Wareham, John J. P. Kastelein, Kay-Tee Khaw, Pieter W. Kamphuisen, Geesje M. Dallinga-Thie

Research output: Contribution to journalArticleAcademicpeer-review

39 Citations (Scopus)

Abstract

Low levels of high-density lipoprotein cholesterol (HDL-C) are a risk factor for coronary artery disease (CAD) and possibly for deep venous thrombosis (DVT). Endothelial lipase is involved in HDL-C metabolism. Common variants in the endothelial lipase gene (LIPG) have been reported to be associated with HDL-C levels and atherothrombosis, but these findings were not consistent. We determined whether five tagging single nucleotide polymorphisms (SNP) in LIPG were associated with lipid parameters, the risk of CAD and the risk of DVT. We used the prospective case-control study nested in the EPIC-Norfolk cohort (1138 CAD cases, 2237 matched controls) for the initial association study and, subsequently, the ACT study (185 patients with documented DVT, 586 patients in which DVT was ruled out) to replicate our findings regarding DVT risk. In EPIC-Norfolk, we found that the minor allele of one SNP, rs2000813 (p.T111I), was associated with moderately higher HDL-C and apolipoprotein A-I levels, higher HDL particle number and larger HDL size. No variants were associated with CAD risk, but three variants were associated with DVT risk (odds ratios 0.60 [95%CI 0.43-0.84], 2.04 [95%CI 1.40-2.98] and 1.67 [95%CI 1.18-2.38] per minor allele for rs2000813, rs6507931 and rs2097055 respectively, p <0.005 for each). However, the association between LIPG SNPs and DVT risk could not be replicated in the ACT study. Our data support a modest association between the LIPG rs2000813 variant and parameters of HDL metabolism, but no association between common genetic variants in LIPG and CAD or DVT risk
Original languageEnglish
Pages (from-to)558-564
JournalAtherosclerosis
Volume211
Issue number2
DOIs
Publication statusPublished - 2010

Cite this