Key result
Baseline hs-cTnI >32.6 pg/mL was associated with a significantly higher risk of MACEs compared with <10.1 pg/mL in haemodialysis patients (HR 1.92; 95% CI 1.57-2.35).
Why the study?
Patients with end-stage kidney disease undergoing haemodialysis have a high risk of cardiovascular events, but the predictive value of hs-cTnI for major adverse cardiac events and mortality needed evaluation.
Does baseline hs-cTnI predict MACEs, cardiovascular death, and all-cause death in patients with ESKD undergoing haemodialysis?
RCT (n=2,776)
double-blind
randomized
Yes
Does baseline hs-cTnI predict MACEs, cardiovascular death, and all-cause death in patients with ESKD undergoing haemodialysis?
Effect estimate: HR 1.92 (95% CI 1.57-2.35)
Baseline hs-cTnI is a strong, independent predictor of MACEs, cardiovascular death, and all-cause mortality in patients with end-stage kidney disease on hemodialysis.
Background Patients with end-stage kidney disease (ESKD) undergoing haemodialysis (HD) have a high risk of cardiovascular (CV) events. This study evaluated troponin I (hs-cTnI) as a predictor of major adverse cardiac events (MACEs), CV death and all-cause death. Methods The AURORA trial, a multicentre, randomized, double-blind trial involved 2776 HD patients comparing rosuvastatin with placebo. No significant effect was found on the composite primary endpoint of CV death, non-fatal myocardial infarction or non-fatal stroke. In this post hoc analysis, we analysed the association between baseline hs-cTnI and outcomes using Cox regression analyses. We adjusted for multiple background factors and available biomarkers. Hs-cTnI was log2-transformed and modelled using a four-knot restricted cubic spline. Variables were ordered by their importance in the models using χ2 value minus degrees of freedom. Results Baseline median hs-cTnI was 17.3 pg/mL. During follow-up, 734 MACEs, 598 CV deaths, and 1094 total deaths occurred. Patients in the upper quartile of hs-cTnI (>32.6 pg/mL) had significantly higher risk of MACEs [hazard ratio (HR) 1.92; 95% confidence interval (CI) 1.57–2.35], CV death (HR 2.12; 95% CI 1.69–2.66), all-cause death (HR 1.84; 95% CI 1.55–2.17) and non-CV death (HR 1.59; 95% CI 1.23–2.05) after full adjustment compared with those in the lowest quartile (<10.1 pg/mL). Hs-cTnI was identified as the strongest predictor for MACEs, CV death, and all-cause death, but not for non-CV death. Conclusions Baseline hs-cTnI is a strong and independent predictor for MACEs and death in patients with ESKD undergoing haemodialysis.
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Tydén et al. (2025) conducted an RCT in end-stage kidney disease (ESKD) undergoing haemodialysis (HD) (n=2,776). hs-cTnI >32.6 pg/mL vs. hs-cTnI <10.1 pg/mL was evaluated on major adverse cardiac events (MACEs) (HR 1.92, 95% CI 1.57-2.35). Baseline hs-cTnI >32.6 pg/mL was associated with a significantly higher risk of MACEs compared with <10.1 pg/mL in haemodialysis patients (HR 1.92; 95% CI 1.57-2.35).
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