Clinical Chemistry
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Clinical Chemistry 55: 109-116, 2009. First published November 6, 2008; 10.1373/clinchem.2008.106500
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(Clinical Chemistry. 2009;55:109-116.)
© 2009 American Association for Clinical Chemistry, Inc.


Proteomics and Protein Markers

Clinical Performance of Two Highly Sensitive Cardiac Troponin I Assays

Per Venge1,a, Stefan James2,3, Leif Jansson4 and Bertil Lindahl2,3

1 Department of Medical Sciences, Clinical Chemistry, University of Uppsala; 2 Department of Medical Sciences, Cardiology, University of Uppsala; 3 Uppsala Clinical Research Centre, University of Uppsala, Uppsala, Sweden; 4 Department of Clinical Chemistry, County Hospital of Gävle, Gävle, Sweden.

aAddress correspondence to this author at: Department of Clinical Chemistry and Pharmacology, University Hospital, SE-751 85 Uppsala, Sweden. Fax +46186113703; e-mail per.venge{at}akademiska.se.

Background: The aim of this study was to compare the clinical performance of 2 sensitive cTnI assays with 10% CV imprecision below the 99th percentile upper reference limit.

Methods: We measured cardiac troponin and N-terminal pro-brain natriuretic peptide (NT-proBNP) concentrations in a random sample of the Global Use of Strategies To Open Occluded Coronary Arteries (GUSTO) IV cohort (n = 1251). Outcome data of 1-year mortality and the composite endpoint DMI [death and/or myocardial infarction (MI) within 30 days] were available in all patients. The 99th percentile of a healthy population was estimated from the Sweden Women and Men and Ischemic Heart Disease (SWISCH) cohort (n = 442). We measured cardiac troponin I (cTnI) using the Access AccuTnI (Beckman Coulter) and Centaur TnI Ultra (Siemens Healthcare Diagnostics) and NT-proBNP using the Elecsys 2010 (Roche Diagnostics).

Results: Applying the 10% CV cutoff, the sensitivity of the Access AccuTnI assay in identifying DMI and death was higher than that of the Centaur TnI Ultra (P = 0.02 and P < 0.001), and the AccuTnI assay also identified more patients at risk (P < 0.001) and with poor outcome. Applying the 99th percentile cutoffs, AccuTnI identified more patients at risk than the Centaur TnI (P < 0.001) and with significant differences in outcome. Significantly more patients with cardiac troponins below the cutoffs as measured by Centaur TnI had increased NT-proBNP concentrations (P < 0.001) compared with AccuTnI.

Conclusions: The AccuTnI assay identified more patients at risk than the Centaur cTnI Ultra assay. Our results demonstrate the clinical potential of high-sensitivity cardiac troponin assays for the identification of patients at risk of dying from cardiovascular disease.




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