Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6002350 | Thrombosis Research | 2014 | 7 Pages |
IntroductionWe investigated whether genetic variations robustly associated with coronary artery disease are also associated with risk of venous thromboembolism in a well-defined, female case-control study (n = 2753) from Sweden.Materials and Methods39 single nucleotide polymorphisms in 32 loci associated with coronary artery disease in genome-wide association studies were identified in a literature search and genotyped in the ThromboEmbolism Hormone Study (TEHS). Association with venous thromboembolism was assessed by logistic regression.ResultsOnly rs579459 in the ABO locus demonstrated a significant association with VTE. A tentative association between ANRIL and VTE in the discovery analysis failed to replicate in a meta-analysis of 4 independent cohorts (total n = 7181).ConclusionsIt appears that only the ABO locus is a shared risk factor for coronary artery disease and VTE.