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PMID: 20226436 已发表 · ppublish 英语

A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1.

American journal of human genetics ·第 86 卷 ·第 4 期 ·2010-04-22

Morange Pierre-Emmanuel, Bezemer Irene, Saut Noémie, Bare Lance, Burgos Gwenaelle, Brocheton Jessy, Durand Hervé, Biron-Andreani Christine, Schved Jean-Francois, Pernod Gilles, Galan Pilar, Drouet Ludovic, Zelenika Diana, Germain Marine, Nicaud Viviane, Heath Simon, Ninio Ewa, Delluc Aurélien, Münzel Thomas, Zeller Tanja, Brand-Herrmann Stefan-Martin, Alessi Marie-Christine, Tiret Laurence, Lathrop Mark, Cambien François, Blankenberg Stefan, Emmerich Joseph, Trégouët David-Alexandre, Rosendaal Frits R

摘要

To identify genetic susceptibility factors conferring increased risk of venous thrombosis (VT), we conducted a multistage study, following results of a previously published GWAS that failed to detect loci for developing VT. Using a collection of 5862 cases with VT and 7112 healthy controls, we identified the HIVEP1 locus on chromosome 6p24.1 as a susceptibility locus for VT. Indeed, the HIVEP1 rs169713C allele was associated with an increased risk for VT, with an odds ratio of 1.20 (95% confidence interval 1.13-1.27, p = 2.86 x 10(-9)). HIVEP1 codes for a protein that participates in the transcriptional regulation of inflammatory target genes by binding specific DNA sequences in their promoter and enhancer regions. The current results provide the identification of a locus involved in VT susceptibility that lies outside the traditional coagulation/fibrinolysis pathway.

文献信息
期刊
American journal of human genetics
期刊简称
Am J Hum Genet
发表日期
2010-04-22
收录日期
2010-04-12
更新日期
2014-12-04
语言
英语
国家/地区
United States
NLM ID
0370475
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