High-Sensitivity Troponin I in Stable Patients with Atherosclerotic Disease in the TRA 2°P - TIMI 50 Trial

Author:

Eisen Alon1,Bonaca Marc P1,Jarolim Petr1,Scirica Benjamin M1,White Harvey D2,Tendera Michal3,Dellborg Mikael4,Nicolau Jose C5,Morais Joao6,Fox Keith A A7,Bohula Erin A1,Murphy Sabina A1,Braunwald Eugene1,Morrow David A1

Affiliation:

1. Brigham and Women's Hospital and Department of Medicine, Harvard Medical School, Boston, MA

2. Auckland City Hospital, Auckland, New Zealand

3. Medical University of Silesia, Katowice, Poland

4. University of Gothenburg and Sahlgrenska University Hospital/Östra, Gothenburg, Sweden

5. University of São Paulo Medical School, São Paulo, Brazil

6. Santo André's Hospital, Leiria, Portugal

7. University of Edinburgh, Edinburgh, UK

Abstract

Abstract BACKGROUND Cardiac troponin I, measured with a high-sensitivity assay (hs-TnI), is well-established for risk prediction in acute coronary syndromes. However, its prognostic role in stable atherosclerotic disease, particularly for future myocardial infarction (MI), is less well defined. METHODS We measured hs-TnI (Abbott ARCHITECT) in 15833 patients with prior MI, ischemic stroke, or peripheral arterial disease from the placebo-controlled Thrombin Receptor Antagonist in Secondary Prevention of Atherothrombotic Ischemic Events (TRA 2°P)–Thrombolysis in Myocardial Infarction (TIMI) 50 trial of the platelet inhibitor vorapaxar, excluding patients with recent MI (<30 days). hs-TnI was categorized into 5 groups based on the detection limit (1.9 ng/L), 99th percentile reference limit (26 ng/L), and tertiles in between (1.9–26 ng/L), as well as sex-specific reference limits. RESULTS Higher hs-TnI concentration was associated with older age, male sex, and increased atherosclerosis burden. hs-TnI identified a graded 3-year risk of cardiovascular death, MI, or stroke from 5.0% to 18.6% (P < 0.001), driven by cardiovascular death and MI (P < 0.001). This risk was independent of established clinical risk indicators, B-type natriuretic peptide and C-reactive protein [adjusted hazard ratio 2.70 (95% CI, 1.96–3.71), P < 0.001 for hs-TnI >26 ng/L vs <1.9 ng/L]. In patients with prior MI, there was a pattern of greater absolute benefit with vorapaxar in patients with an increased hs-TnI (absolute risk difference 1.9% with hs-TnI >26 ng/L vs 0.3% with hs-TnI <1.9 ng/L; P interaction = 0.82). CONCLUSIONS In stable patients with established atherosclerosis, hs-TnI concentrations effectively stratified the risk of new or recurrent cardiovascular (CV) events, in particular CV death and MI. High-risk patients with prior MI identified by increased hs-TnI had a substantial absolute improvement in net clinical outcome with vorapaxar.

Funder

The TRA 2°P-TIMI 50

Merck & Co. Reagent

Abbott Laboratories

Publisher

Oxford University Press (OUP)

Subject

Biochemistry, medical,Clinical Biochemistry

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