Key result
High-sensitive troponin I >0 ng/ml was associated with the primary composite outcome (RR 2.360; 95% CI 1.359-4.099; p=0.001), but statistical significance was lost after controlling for age.
Why the study?
Does hs-cTnI >0 ng/ml predict the composite of acute ischemic events, heart failure, or death in patients with stable coronary artery disease?
Cohort (n=705)
Does hs-cTnI >0 ng/ml predict the composite of acute ischemic events, heart failure, or death in patients with stable coronary artery disease?
Relative Risk: 2.36 (95% CI 1.359–4.099)
p-value: p=0.001
In stable coronary artery disease, the prognostic value of hs-cTnI >0 ng/ml for adverse cardiovascular outcomes is confounded by age and other clinical variables.
hs-cTnI >0 ng/ml should not guide prognostication in stable CAD; leaves open independent value after age adjustment in future cohorts.
OBJECTIVES: To study the prognostic value of high-sensitive troponin (hs-cTn) I in stable coronary artery disease. METHODS: In total, we studied 705 patients. Secondary outcomes were the incidence of: (1) acute ischemic events and (2) heart failure or death. The primary outcome was the composite of them. RESULTS: Patients with hs-cTnI >0 ng/ml (62.1%) were older, had a lower estimated glomerular filtration rate, more frequent a history of hypertension, atrial fibrillation, ejection fraction <40%, and therapy with angiotensin-converting enzyme inhibitors, diuretics and acenocumarol. The follow-up period was 2.2 ± 0.99 years. Fifty-three patients suffered an acute ischemic event, 33 died or suffered heart failure and 78 developed the primary outcome. By univariate Cox's regression analysis, hs-cTnI >0 was associated with a higher risk of developing the primary outcome [relative risk = 2.360 (1.359-4.099); p = 0.001] and heart failure or death [relative risk = 5.932 (1.806-19.482); p < 0.001], but not with acute ischemic events. Statistical significance was lost after controlling for age. By logistic regression analysis, age [relative risk = 1.026 (1.009-1.044); p = 0.003], ejection fraction <40% [relative risk = 4.099 (2.043-8.224); p < 0.001], use of anticoagulants [relative risk = 2.785 (1.049-7.395); p = 0.040] and therapy with angiotensin-converting enzyme inhibitors [relative risk = 1.471 (1.064-2.034); p = 0.020], and estimated glomerular filtration rate [relative risk = 0.988 (0.977-0.999); p = 0.027] were associated with hs-cTnI >0. CONCLUSIONS: In stable coronary disease, hs-cTnI is associated with the incidence of heart failure or death, but this relationship depends on other variables.
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Carda et al. (2015) conducted a cohort in Stable coronary artery disease (n=705). High-sensitive troponin I >0 ng/ml vs. High-sensitive troponin I = 0 ng/ml was evaluated on Composite of acute ischemic events and heart failure or death (RR 2.360, 95% CI 1.359-4.099, p=0.001). High-sensitive troponin I >0 ng/ml was associated with the primary composite outcome (RR 2.360; 95% CI 1.359-4.099; p=0.001), but statistical significance was lost after controlling for age.
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