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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 (CROSBI ID 212538)

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Yu, B. ; Barbalić, M. 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 // Circulation. Cardiovascular genetics, 6 (2013), 1; 82-88. doi: 10.1161/CIRCGENETICS.112.963058

Podaci o odgovornosti

Yu, B. ; Barbalić, M.

engleski

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

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. 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). 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.

genetics ; genome-wide association study ; troponin

On behalf of ECARDIoGRAM Consortium.

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Podaci o izdanju

6 (1)

2013.

82-88

objavljeno

1942-325X

1942-3268

10.1161/CIRCGENETICS.112.963058

Povezanost rada

nije evidentirano

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