Cardiac Troponins and Cardiovascular Disease Risk Prediction

Anoop SV Shah ORCID logo ; Spencer J Keene ; Lisa Pennells ORCID logo ; Stephen Kaptoge ; Dorien M Kimenai ; Matthew Walker ; Julianne D Halley ; Sara Rocha ; Ron C Hoogeveen ORCID logo ; Vilmundur Gudnason ; +62 more... Stephan JL Bakker ; Sasiwarang G Wannamethee ; Manan Pareek ; Kai M Eggers ORCID logo ; J Wouter Jukema ; Graeme J Hankey ; James A deLemos ; Ian Ford ; Torbjørn Omland ORCID logo ; Magnus Nakrem Lyngbakken ; Bruce M Psaty ; Christopher R deFilippi ORCID logo ; Angela M Wood ; John Danesh ; Paul Welsh ; Naveed Sattar ORCID logo ; Nicholas L Mills ; Emanuele Di Angelantonio ; Ingunn Thorsteinsdottir ; Elias F Gudmundsson ; Lenore J Launer ; Vilmundur Gudnason ; Vijay Nambi ; Christie M Ballantyne ; Xiaoming Jia ; Ron C Hoogeveen ; Peter H Whincup ; Sasiwarang G Wannamethee ; Bruce Psaty ; Stephen Selinger ; Jorge R Kizer ; Colby Ayers ; Rebecca Vigen ; James A deLemos ; Archie Campbell ; Caroline Hayward ; Catherine Sudlow ; Anoop SV Shah ; Osvaldo P Almeida ; Damon A Bell ; Leon Flicker ; Graeme J Hankey ; Torbjorn Omland ; Magnus Lyngbakken ; Christopher R DeFilippi ; Michael H Olsen ; Peter M Nilsson ; Deepak L Bhatt ; Manan Pareek ; Björn Zethelius ; Lars Lind ; Kai M Eggers ; Stephan JL Bakker ; Lyanne M Kieneker ; Ronald T Gansevoort ; Ian Ford ; Naveed Sattar ; Stella Trompet ; J Wouter Jukema ; Pablo Perel ORCID logo ; Kuan-Ken Lee ; David McAllister ; (2025) Cardiac Troponins and Cardiovascular Disease Risk Prediction. Journal of the American College of Cardiology, 85 (14). pp. 1471-1484. ISSN 0735-1097 DOI: 10.1016/j.jacc.2025.02.016
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<h4>Background</h4>The extent to which high-sensitivity cardiac troponin can predict cardiovascular disease (CVD) is uncertain.<h4>Objectives</h4>We aimed to quantify the potential advantage of adding information on cardiac troponins to conventional risk factors in the prevention of CVD.<h4>Methods</h4>We meta-analyzed individual-participant data from 15 cohorts, comprising 62,150 participants without prior CVD. We calculated HRs, measures of risk discrimination, and reclassification after adding cardiac troponin T (cTnT) or I (cTnI) to conventional risk factors. The primary outcome was first-onset CVD (ie, coronary heart disease or stroke). We then modeled the implications of initiating statin therapy using incidence rates from 2.1 million individuals from the United Kingdom.<h4>Results</h4>Among participants with cTnT or cTnI measurements, 8,133 and 3,749 incident CVD events occurred during a median follow-up of 11.8 and 9.8 years, respectively. HRs for CVD per 1-SD higher concentration were 1.31 (95% CI: 1.25-1.37) for cTnT and 1.26 (95% CI: 1.19-1.33) for cTnI. Addition of cTnT or cTnI to conventional risk factors was associated with C-index increases of 0.015 (95% CI: 0.012-0.018) and 0.012 (95% CI: 0.009-0.015) and continuous net reclassification improvements of 6% and 5% in cases and 22% and 17% in noncases. One additional CVD event would be prevented for every 408 and 473 individuals screened based on statin therapy in those whose CVD risk is reclassified from intermediate to high risk after cTnT or cTnI measurement, respectively.<h4>Conclusions</h4>Measurement of cardiac troponin results in a modest improvement in the prediction of first-onset CVD that may translate into population health benefits if used at scale.

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