A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1.
case_control · Level III
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- Record sourced from PubMed, PMID 20226436.
- Also identified by DOI 10.1016/j.ajhg.2010.02.011 and PMC identifier 2850428.
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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.
Medical subject headings
- Chromosomes, Human, Pair 6
- DNA-Binding Proteins
- Genetic Predisposition to Disease
- Genome-Wide Association Study
- Polymorphism, Single Nucleotide
- Transcription Factors
- Venous Thrombosis