4.7 Article

Prognostic Value of Cardiac Troponin I Measured With a Highly Sensitive Assay in Patients With Stable Coronary Artery Disease

Journal

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
Volume 61, Issue 12, Pages 1240-1249

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacc.2012.12.026

Keywords

cardiovascular death; coronary artery disease; natriuretic peptides; troponin

Funding

  1. National Heart, Lung, and Blood Institute with support from Knoll Pharmaceuticals and Abbott Laboratories
  2. Abbott Diagnostics and Roche Diagnostics
  3. Abbott Diagnostics and Roche Diagnostics through Akershus University Hospital
  4. Amgen
  5. Anthera
  6. AstraZeneca
  7. Biogen
  8. Boehringer Ingelheim
  9. Boston Scientific
  10. Bristol-Myers Squibb
  11. Cytokinetics
  12. Daiichi-Sankyo
  13. Genzyme
  14. Gilead
  15. GlaxoSmithKline
  16. Medtronic
  17. Nicox
  18. Novartis
  19. Roche
  20. Salutria
  21. Sanofi-Aventis
  22. Servier
  23. University of Oxford
  24. VIA Pharmaceutics
  25. Abbott
  26. Baxter
  27. Celladon
  28. Abbott Laboratories
  29. BRAHMS
  30. Critical Diagnostics
  31. Roche Diagnostics through Brigham
  32. Women's Hospital
  33. Knoll Pharmaceuticals

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Objectives The aims of this study were to assess the prognostic value of cardiac troponin I levels, measured with a new high-sensitivity assay, in low-risk patients with stable coronary artery disease (CAD) and to contrast its determinants and prognostic merit with that of high-sensitivity cardiac troponin T (hs-TnT). Background New, highly sensitive cardiac troponin assays permit evaluation of the association between troponin levels and outcomes in patients with stable CAD. Methods High-sensitivity cardiac troponin I (hs-TnI) levels at baseline were assessed in 3,623 patients with stable CAD and preserved systolic function enrolled in the PEACE (Prevention of Events With Angiotensin-Converting Enzyme Inhibitor Therapy) trial. Results In total, 98.5% of patients had hs-TnI concentrations higher than the detection level (1.2 pg/ml). hs-TnI correlated moderately with hs-TnT (r = 0.44) and N-terminal pro-B-type natriuretic peptide (r = 0.39) but only weakly with age (r = 0.17) and estimated glomerular filtration rate (r = -0.11). During a median follow-up period of 5.2 years, 203 patients died of cardiovascular causes or were hospitalized for heart failure, and 209 patients had nonfatal myocardial infarctions. In analyses adjusting for conventional risk markers, N-terminal pro-B-type natriuretic peptide, and hs-TnT, hs-TnI levels in the fourth compared with the 3 lower quartiles were associated with the incidence of cardiovascular death or heart failure (hazard ratio: 1.88; 95% confidence interval: 1.33 to 2.66; p < 0.001). There was a significant, albeit weaker association with nonfatal myocardial infarction (hazard ratio: 1.44; 95% confidence interval: 1.03 to 2.01; p = 0.031). In the same models, hs-TnT concentrations were associated with the incidence of cardiovascular death or heart failure but not of myocardial infarction. Conclusions In patients with stable CAD, hs-TnI concentrations are associated with cardiovascular risk independently of conventional risk markers and hs-TnT. (Prevention of Events With Angiotensin-Converting Enzyme Inhibitor Therapy [PEACE]; NCT00000558) (J Am Coll Cardiol 2013;61:1240-9) (C) 2013 by the American College of Cardiology Foundation

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