Serial high-sensitivity cardiac troponin I trajectories predict cardiovascular events in hemodialysis patients
Yue Wu1, Fengqin Li1, Qiao Fu1
1Department of Nephrology, Shanghai Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Insights
Serial changes in high-sensitivity cardiac troponin I (hs-cTnI) levels independently predict cardiovascular events in maintenance hemodialysis (MHD) patients. Dynamic hs-cTnI monitoring can aid prognosis and early intervention in this high-risk group.
Area of Science:
- Nephrology
- Cardiology
- Biomarkers
Background:
- Elevated high-sensitivity cardiac troponin I (hs-cTnI) is common in maintenance hemodialysis (MHD) patients.
- The prognostic value of serial hs-cTnI changes in MHD patients without evident myocardial ischemia is not well understood.
Purpose of the Study:
- To investigate the association between longitudinal hs-cTnI trajectories and major adverse cardiovascular events (MACE) in MHD patients.
Main Methods:
- Retrospective cohort study of 265 MHD patients with repeated hs-cTnI measurements.
- Analysis of nonlinear relationships using restricted cubic splines and time-dependent Cox models.
- Investigation of hs-cTnI association with MACE using baseline and repeated measurements.
Main Results:
- The incidence of MACE was 41.9% among 265 MHD patients.
- An inflection point for hs-cTnI and MACE risk was identified at 64 ng/L.
- Increased hs-cTnI levels, both baseline and time-updated, were significantly associated with elevated MACE risk.
Conclusions:
- Serial hs-cTnI changes are independent predictors of cardiovascular risk in MHD patients.
- Dynamic hs-cTnI measurement may enhance cardiovascular prognosis monitoring and guide early interventions in MHD patients.
Background:
Although commonly elevated in maintenance hemodialysis (MHD) patients without apparent myocardial ischemia, the prognostic significance of serial high-sensitivity cardiac troponin I (hs-cTnI) changes remains underexplored. We aimed to evaluate the association between longitudinal hs-cTnI trajectories and cardiovascular events in MHD patients.
Methods:
This retrospective cohort study enrolled 265 clinically stable MHD patients with repeated hs-cTnI measurements (mean six per patient) and followed them until the first major adverse cardiovascular event (MACE) or January 2024. Nonlinear relationships were analyzed using restricted cubic splines, with inflection points identified to assess threshold and saturation effects. Multivariate regression analyses, time-dependent Cox and splines for time were used to investigate the association of hs-cTnI with MACE using single time point (at baseline) and repeated measurements, respectively.
Results:
Among 265 MHD patients, the incidence of MACE was 41.9%. Nonlinear relationships between hs-cTnI and MACE were identified, with an inflection point at 64 ng/L. Multiple regression equations showed a 2.06-fold increased risk of MACE in the high baseline hs-cTnI group compared with the low baseline hs-cTnI group after adjusting for numerous influencing factors. After full adjustment, each 10 ng/L increase in the time-updated hs-cTnI value remained significantly associated with a 2.71% elevated risk of MACE. Splines for time demonstrated that patients with MACE exhibited higher hs-cTnI concentrations and steeper trajectories compared with those without MACE.
Conclusion:
Serial hs-cTnI changes independently predict cardiovascular risk in MHD patients, suggesting that dynamic measurement of hs-cTnI may be useful for monitoring cardiovascular prognosis and early intervention in this high-risk population.
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