Association of High-sensitivity Cardiac Troponin T with Mortality and Cardiovascular Events in a Community-based Prospective Study in Beijing
Overview
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Objective: The prognostic value of cardiac troponins in apparently healthy populations is not well established. The aim of this study was to investigate the prognostic properties of high-sensitivity cardiac troponin T (hs-cTnT) for long-term adverse outcomes.
Setting: A community-dwelling prospective survey of residents from two communities in Beijing.
Participants: From September 2007 to January 2009, 1680 participants were initially enrolled. Of these, 1499 (870 females, mean age: 61.4 years) participants completed the survey and were followed up for a median of 4.8 years (IQR: 4.5-5.2).
Outcome Measures: The primary outcome was the occurrence of all-cause mortality and major cardiovascular events.
Results: Overall, 820 individuals (54.7%) had detectable hs-cTnT levels. During the follow-up, 52 participants (3.5%) died, 154 (10.3%) had major cardiovascular events and 99 (6.6%) experienced new-onset coronary events. Compared with those with undetectable hs-cTnT levels, participants with hs-cTnT levels in the highest category (≥14 ng/L) had a significantly increased risk for all-cause mortality (adjusted HR (aHR): 2.07, 95% CI 1.05 to 3.01), major cardiovascular events (aHR: 3.27, 95% CI 1.88 to 5.70) and coronary events (aHR: 4.50, 95% CI 2.26 to 9.02) in covariate-adjusted analyses. No differences in stroke incidence were found (aHR: 1.27, 95% CI 0.69 to 2.62). Also, significant associations were presented when hs-cTnT levels were modelled as a continuous variable and when analysing changes in hs-cTnT levels over time with adverse outcomes. The addition of troponin T levels to clinical variables led to significant increases in risk prediction with a marked improvement in the C-statistics (p=0.003 or lower).
Conclusions: In this cohort of individuals from a community-based population, cTnT levels measured with a highly sensitive assay were associated with increases in the subsequent risk for all-cause mortality and major cardiovascular events. These results might support screening for at-risk individuals.
Kobayashi T, Nasu T, Satoh M, Kotozaki Y, Tanno K, Asahi K Am Heart J Plus. 2024; 22:100212.
PMID: 38558906 PMC: 10978419. DOI: 10.1016/j.ahjo.2022.100212.
Tedla Y, Driver S, Szklo M, Kuller L, Lima J, Michos E Am J Prev Cardiol. 2023; 13:100471.
PMID: 36873803 PMC: 9975219. DOI: 10.1016/j.ajpc.2023.100471.
Lind L, Loader J, Lindahl B, Eggers K, Sundstrom J PLoS One. 2022; 17(7):e0271835.
PMID: 35877671 PMC: 9312363. DOI: 10.1371/journal.pone.0271835.
Imano H, Yamagishi K, Ohira T, Kitamura A, Okada T, Muraki I J Atheroscler Thromb. 2022; 30(3):237-246.
PMID: 35569956 PMC: 9981345. DOI: 10.5551/jat.63378.
Cao R, Fang Z, Li S, Xu M, Zhang J, Han D Front Physiol. 2020; 11:1104.
PMID: 33041846 PMC: 7522524. DOI: 10.3389/fphys.2020.01104.