Naslov
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
(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)

Autori
Yu, B. ; Barbalić, M.

Izvornik
Circulation. Cardiovascular genetics (1942-325X) 6 (2013), 1; 82-88

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
genetics ; genome-wide association study ; troponin

Sažetak
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.

Izvorni jezik
Engleski

Napomena
On behalf of ECARDIoGRAM Consortium.

POVEZANOST RADA