Literature DB >> 29038153

Prospective Validation of a Biomarker-Based Rule Out Strategy for Functionally Relevant Coronary Artery Disease.

Joan E Walter1, Ursina Honegger1, Christian Puelacher1,2, Deborah Mueller1, Max Wagener1,2, Nicolas Schaerli1,2, Ivo Strebel1, Raphael Twerenbold1,3, Jasper Boeddinghaus1,2, Thomas Nestelberger1,2, Lorraine Sazgary1,2, Stella Marbot1,2, Jeanne du Fay de Lavallaz1, Christoph Kaiser1, Stefan Osswald1, Damian Wild4, Katharina Rentsch5, Michael Zellweger1, Tobias Reichlin1, Christian Mueller6.   

Abstract

BACKGROUND: This study aimed to prospectively advance a rule-out strategy for functionally significant coronary artery disease (CAD) by use of high-sensitivity cardiac troponin I (hs-cTnI) from bench to bedside, by application of a 3-step approach: validation in serum, correlation in plasma, and application on a clinical platform.
METHODS: Patients without known CAD referred for rest/stress myocardial perfusion single-photon emission tomography/computer tomography (MPI-SPECT/CT) were assigned to 3 consecutive cohorts: validation, correlation, and application. Functionally relevant CAD was adjudicated with the use of expert interpretation of MPI-SPECT/CT and, if available, coronary angiography. In the validation cohort resting hs-cTnI was measured in serum before stress testing with the research Erenna system, in serum and plasma in the correlation cohort with the research Erenna system, and in plasma in the application cohort with the clinical Clarity system.
RESULTS: Overall, functionally relevant CAD was adjudicated in 21% (304/1478) of patients. In the validation cohort (n = 613), hs-cTnI concentrations were significantly higher in patients with functionally relevant CAD (median 2.8 ng/L vs 1.9 ng/L, P < 0.001) as compared to patients without functionally relevant CAD and allowed a rule out with 95% sensitivity in 14% of patients. In the correlation cohort (n = 606), hs-cTnI concentrations in serum and plasma strongly correlated (Spearman r = 0.921) and had similar diagnostic accuracy as quantified by the area under the receiver operating characteristic curve (0.686 vs 0.678, P = 0.425). In the application cohort (n = 555), very low hs-cTnI plasma concentrations (< 0.5 ng/L) ruled out functionally relevant CAD with 95% sensitivity in 10% of patients.
CONCLUSIONS: A single resting plasma hs-cTnI measurement can safely rule out functionally relevant CAD in around 10% of patients without known CAD.
© 2017 American Association for Clinical Chemistry.

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Year:  2017        PMID: 29038153     DOI: 10.1373/clinchem.2017.277210

Source DB:  PubMed          Journal:  Clin Chem        ISSN: 0009-9147            Impact factor:   8.327


  5 in total

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Journal:  J Clin Microbiol       Date:  2018-10-25       Impact factor: 5.948

2.  Coronary Atherosclerosis, Cardiac Troponin, and Interleukin-6 in Patients With Chest Pain: The PROMISE Trial Results.

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Journal:  JACC Cardiovasc Imaging       Date:  2022-05-11

3.  Cardiopulmonary Exercise Testing and Cardiac Biomarker Measurements in Young Football Players: A Pilot Study.

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Journal:  J Clin Med       Date:  2022-05-14       Impact factor: 4.964

4.  Highly sensitive troponin I assay in the diagnosis of coronary artery disease in patients with suspected stable angina.

Authors:  Indra Ramasamy
Journal:  World J Cardiol       Date:  2021-12-26

5.  Gut microbiota-dependent metabolite trimethylamine N-oxide (TMAO) and cardiovascular risk in patients with suspected functionally relevant coronary artery disease (fCAD).

Authors:  Melissa Amrein; Xinmin S Li; Joan Walter; Zeneng Wang; Tobias Zimmermann; Ivo Strebel; Ursina Honegger; Kathrin Leu; Ibrahim Schäfer; Raphael Twerenbold; Christian Puelacher; Noemi Glarner; Thomas Nestelberger; Luca Koechlin; Benjamin Ceresa; Philip Haaf; Adam Bakula; Michael Zellweger; Stanley L Hazen; Christian Mueller
Journal:  Clin Res Cardiol       Date:  2022-02-26       Impact factor: 6.138

  5 in total

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