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Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.

Authors :
Yu B
Barbalic M
Brautbar A
Nambi V
Hoogeveen RC
Tang W
Mosley TH
Rotter JI
deFilippi CR
O'Donnell CJ
Kathiresan S
Rice K
Heckbert SR
Ballantyne CM
Psaty BM
Boerwinkle E
Source :
Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2013 Feb; Vol. 6 (1), pp. 82-8. Date of Electronic Publication: 2012 Dec 16.
Publication Year :
2013

Abstract

Background: High levels of cardiac troponin T, measured by a highly sensitive assay (hs-cTnT), are strongly associated with incident coronary heart disease and heart failure. To date, no large-scale genome-wide association study of hs-cTnT has been reported. We sought to identify novel genetic variants that are associated with hs-cTnT levels.<br />Methods and Results: We performed a genome-wide association in 9491 European Americans and 2053 blacks free of coronary heart disease and heart failure from 2 prospective cohorts: the Atherosclerosis Risk in Communities Study and the Cardiovascular Health Study. Genome-wide association studies were conducted in each study and race stratum. Fixed-effect meta-analyses combined the results of linear regression from 2 cohorts within each race stratum and then across race strata to produce overall estimates and probability values. The meta-analysis identified a significant association at chromosome 8q13 (rs10091374; P=9.06×10(-9)) near the nuclear receptor coactivator 2 (NCOA2) gene. Overexpression of NCOA2 can be detected in myoblasts. An additional analysis using logistic regression and the clinically motivated 99th percentile cut point detected a significant association at 1q32 (rs12564445; P=4.73×10(-8)) in the gene TNNT2, which encodes the cardiac troponin T protein itself. The hs-cTnT-associated single-nucleotide polymorphisms were not associated with coronary heart disease in a large case-control study, but rs12564445 was significantly associated with incident heart failure in Atherosclerosis Risk in Communities Study European Americans (hazard ratio=1.16; P=0.004).<br />Conclusions: We identified 2 loci, near NCOA2 and in the TNNT2 gene, at which variation was significantly associated with hs-cTnT levels. Further use of the new assay should enable replication of these results.

Details

Language :
English
ISSN :
1942-3268
Volume :
6
Issue :
1
Database :
MEDLINE
Journal :
Circulation. Cardiovascular genetics
Publication Type :
Academic Journal
Accession number :
23247143
Full Text :
https://doi.org/10.1161/CIRCGENETICS.112.963058