Key result
High-sensitivity cardiac troponin I lost independent prognostic value for 180-day mortality in AHF (HR 1.07, p=0.18) as 69% of its effect was mediated by inflammation, congestion, and renal function.
Why the study?
Does systemic inflammation (hs-CRP), hemodynamic congestion (BNP), and renal impairment (eGFR) mediate the prognostic association between high-sensitivity cardiac troponin I (hs-cTnI) and all-cause mortality in patients hospitalized with acute heart failure?
Cohort (n=431)
No
Does systemic inflammation (hs-CRP), hemodynamic congestion (BNP), and renal impairment (eGFR) mediate the prognostic association between high-sensitivity cardiac troponin I (hs-cTnI) and all-cause mortality in patients hospitalized with acute heart failure?
Answers are grounded in this paper and cite their sources.
In acute heart failure, the prognostic association between elevated high-sensitivity cardiac troponin I and 180-day mortality is largely mediated (69%) by coexisting systemic inflammation, hemodynamic congestion, and renal dysfunction rather than representing an isolated marker of myocardial injury.
Introduction Cardiac troponin is recognized as a strong predictor of mortality in patients with acute heart failure (AHF). The aim of this study was to evaluate the prognostic impact of high-sensitivity cardiac troponin I (hs-cTnI) on mortality risk in patients with AHF in relation to inflammatory, congestion, and renal indices. Methods We enrolled 431 patients (79 ± 10 years, 51% male) with AHF. At admission, hemodynamic congestion, inflammatory status, and renal function were assessed by means of brain natriuretic peptide (BNP, ng/l), high-sensitivity C-reactive protein (hs-CRP, mg/l), and estimated glomerular filtration rate (eGFR, ml/min), respectively. Mediation analyses were performed to assess the presence and magnitude of these components. Results The cumulative incidence of mortality at 180-day follow-up was 36%. hs-cTnI significantly correlated with BNP (r = 0.28), hs-CRP (r = 0.31), and eGFR (r = − 0.23); these variables explained 18% of the overall variability in hs-cTnI. In univariate Cox regression analysis, hs-cTnI, hs-CRP, BNP, and eGFR were predictors of all-cause death. The association between hs-cTnI and mortality was largely mediated by inflammation, congestion, and renal function, which collectively explained 69% of the total effect. In multivariate analysis, only ln hs-CRP (HR: 1.21; 1.08–1.37), ln BNP (HR: 1.37; 1.09–1.74), and eGFR (HR: 0.99; 0.98–1.00) remained independent predictors of mortality. Conclusions Elevated troponin levels in AHF might be influenced by the coexistence of systemic inflammation, hemodynamic congestion, and renal dysfunction. Therefore, circulating troponin in AHF may be considered an integrated biomarker reflecting multiple pathophysiological processes.
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Scicchitano et al. (2026) conducted a cohort in Acute heart failure (AHF) (n=431). High-sensitivity cardiac troponin I (ln hs-cTnI) assessed with mediators (hs-CRP, BNP, eGFR) was evaluated on 180-day all-cause mortality (multivariate Model 3 adjusted for clinical confounders, BNP, eGFR, and hs-CRP) (HR 1.07, 95% CI 0.97-1.17, p=0.18). High-sensitivity cardiac troponin I lost independent prognostic value for 180-day mortality in AHF (HR 1.07, p=0.18) as 69% of its effect was mediated by inflammation, congestion, and renal function.
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