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Author Notes:

Correspondence: Arshed A. Quyyumi, MD, Division of Cardiology, Department of Medicine, Emory Clinical Cardiovascular Research Institute, Emory University School of Medicine, 1760 Haygood Dr NE, Atlanta, GA 30322. Email: aquyyum@emory.edu

Competing interests: Dr Murtagh is a full‐time Abbott employee and shareholder of Abbott. The remaining authors have no disclosures to report.

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Research Funding:

A.A.Q. has been supported by National Institute of Health grants P01HL154996‐01A1, R33HL138657‐05, U54AG062334‐01, P30DK111024‐07S2, R61HL154116‐01, R01HL109413‐07, R01HL166004‐01, 15SFCRN23910003, 5P01HL086773‐09, 5P01HL101398‐05, and 1P20HL113451‐04.

Keywords:

  • chronic total occlusion
  • coronary artery bypass graft
  • high sensitivity troponin‐I
  • percutaneous coronary intervention
  • cardiology

High Sensitivity Troponin Level and Benefits of Chronic Total Occlusion Revascularization

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Journal Title:

Journal of the American Heart Association

Volume:

Volume 12, Number 21

Publisher:

, Pages e031431-None

Type of Work:

Article | Final Publisher PDF

Abstract:

Background The survival benefit of revascularization of chronic total occlusion (CTO) of the coronary arteries remains a subject of controversy. We measured high sensitivity troponin‐I (hsTn‐I) levels as an estimate of myocardial ischemia in patients with stable coronary artery disease, with the hypothesis that (1) patients with CTO have higher levels of hsTn‐I than patients without CTO, (2) hsTn‐I levels will predict adverse cardiovascular events in patients with CTO, and (3) patients with elevated hsTn‐I levels will have a survival benefit from CTO revascularization. Methods and Results In 428 patients with stable coronary artery disease and CTO undergoing coronary angiography, adverse event rates were investigated. Cox proportional hazards models and Fine and Gray subdistribution hazard models were performed to determine the association between hsTn‐I level and incident event rates in patients with CTO. HsTn‐I levels were higher in patients with compared with those without CTO (median 6.7 versus 5.6 ng/L, P=0.002). An elevated hsTn‐I level was associated with higher adverse event rates (adjusted all‐cause mortality hazard ratio, 1.19 [95% CI, 1.08–1.32]; P=0.030) for every doubling of hsTn‐I level. CTO revascularization was performed in 28.3% of patients. In patients with a high (>median) hsTn‐I level, CTO revascularization was associated with substantially lower all‐cause mortality (adjusted hazard ratio, 0.26 [95% CI, 0.08–0.88]; P=0.030) compared with those who did not undergo revascularization. In patients with a low (<median) hsTn‐I level, event rates were similar in those with and without CTO revascularization. Conclusions HsTn‐I levels may help identify individuals who benefit from CTO revascularization.

Copyright information:

© 2023 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/).
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