# Troponin I is an independent predictor of cardiovascular events and mortality in haemodialysis patients

**Authors:** Maria Tydén, Magnus E Westerlund, Kevin Duarte, Niclas Eriksson, Nicolas Girerd, Bernhard K Krämer, Winfried März, Patrick Rossignol, Hubert Scharnagl, Inga Soveri, Maria K Svensson, Faiez Zannad, Bengt Fellström

PMC · DOI: 10.1093/ckj/sfaf047 · Clinical Kidney Journal · 2025-02-11

## TL;DR

High levels of troponin I predict higher risk of heart problems and death in patients on dialysis, even after adjusting for other factors.

## Contribution

Troponin I is shown to be the strongest independent predictor of cardiovascular events and mortality in hemodialysis patients.

## Key findings

- Patients with the highest troponin I levels had nearly double the risk of major adverse cardiac events.
- Troponin I was the strongest predictor for cardiovascular death and all-cause death in hemodialysis patients.
- No significant effect of rosuvastatin was found on the primary cardiovascular endpoints.

## Abstract

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.

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.

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.

Baseline hs-cTnI is a strong and independent predictor for MACEs and death in patients with ESKD undergoing haemodialysis.

## Linked entities

- **Proteins:** LOC105904758 (troponin I, fast skeletal muscle-like)
- **Chemicals:** rosuvastatin (PubChem CID 446157)
- **Diseases:** end-stage kidney disease (MONDO:0004375)

## Full-text entities

- **Diseases:** stroke (MESH:D020521), ESKD (MESH:D007676), death (MESH:D003643), myocardial infarction (MESH:D009203), CV death (MESH:D002318)
- **Chemicals:** rosuvastatin (MESH:D000068718)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12209788/full.md

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Source: https://tomesphere.com/paper/PMC12209788