Literature DB >> 20226436

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

Pierre-Emmanuel Morange1, Irene Bezemer, Noémie Saut, Lance Bare, Gwenaelle Burgos, Jessy Brocheton, Hervé Durand, Christine Biron-Andreani, Jean-Francois Schved, Gilles Pernod, Pilar Galan, Ludovic Drouet, Diana Zelenika, Marine Germain, Viviane Nicaud, Simon Heath, Ewa Ninio, Aurélien Delluc, Thomas Münzel, Tanja Zeller, Stefan-Martin Brand-Herrmann, Marie-Christine Alessi, Laurence Tiret, Mark Lathrop, François Cambien, Stefan Blankenberg, Joseph Emmerich, David-Alexandre Trégouët, Frits R Rosendaal.   

Abstract

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. (c) 2010 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20226436      PMCID: PMC2850428          DOI: 10.1016/j.ajhg.2010.02.011

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  15 in total

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  18 in total

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