USF1 Gene Variants, Cardiovascular Risk, and Mortality in European Americans
Author(s) -
Alexander P. Reiner,
Christopher S. Carlson,
Nancy S. Jenny,
Jon Peter Durda,
David S. Siscovick,
Deborah A. Nickerson,
Russell P. Tracy
Publication year - 2007
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.107.154559
Subject(s) - dyslipidemia , medicine , odds ratio , linkage disequilibrium , genotype , allele , haplotype , disease , genetics , biology , gene
A common haplotype of the upstream transcription factor 1 gene (USF1) has been associated with decreased susceptibility to familial combined hyperlipidemia (FCHL) and, paradoxically, with increased risk of cardiovascular disease (CVD) and all-cause mortality.
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