Diagnostic and prognostic performance of a novel high-sensitivity cardiac troponin T assay compared to a contemporary sensitive cardiac troponin I assay in patients with acute coronary syndrome

Objective The study sought to compare the clinical performance of two more sensitive cardiac troponin (cTn) assays, a novel high-sensitivity (hs) troponin T assay and a contemporary cTnI assay. Methods We measured hs-cTnT (Roche TnThs) and cTnI (Siemens Centaur Ultra) on presentation in 1,384 patien...

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Veröffentlicht in:Clinical research in cardiology 2012-10, Vol.101 (10), p.837-845
Hauptverfasser: Mueller, M., Celik, S., Biener, M., Vafaie, M., Schwoebel, K., Wollert, K. C., Januzzi, J. L., Katus, H. A., Giannitsis, E.
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Sprache:eng
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Zusammenfassung:Objective The study sought to compare the clinical performance of two more sensitive cardiac troponin (cTn) assays, a novel high-sensitivity (hs) troponin T assay and a contemporary cTnI assay. Methods We measured hs-cTnT (Roche TnThs) and cTnI (Siemens Centaur Ultra) on presentation in 1,384 patients with suspected acute coronary syndrome (ACS) who underwent early invasive strategy within 24 h after presentation. Kaplan–Meier, Cox proportional hazards, and receiver-operating characteristic (ROC) analysis was used to compare their prognostic performance for the prediction of all-cause death and death/MI (myocardial infarction) after a median of 271 days. We also compared the diagnostic performance of these assays on presentation for early diagnosis of non-STEMI. Results Both hs-cTnT and cTnI were independently predictive of long-term death (OR 3.51 vs. 2.19) and the composite of death/MI (OR 9.24 vs. 3.61), across the spectrum of ACS and in patients without ACS. When used as a continuous variable, ROC analysis demonstrated significantly higher areas under the curve (AUC) for hs-cTnT as compared to cTnI for the prediction of death/MI (0.721 vs. 0.672, P  = 0.024), a trend to better prediction of all-cause death (0.721 vs. 0.672, P  = 0.093) and significantly higher AUC for early diagnosis of non-STEMI (0.965 vs. 0.901, P  
ISSN:1861-0684
1861-0692
DOI:10.1007/s00392-012-0469-6