Key result
Top-quintile hs-cTnT is linked to ~3.7-fold higher all-cause mortality in dialysis patients.
Why the study?
Dialysis patients have an exceedingly high mortality rate, and the prognostic value and variability of hs-cTnT and CRP for risk stratification in stable hemodialysis and peritoneal dialysis populations needed evaluation.
Cohort (n=574)
Blinded outcome assessment and laboratory personnel
No
May support hs-cTnT risk stratification in dialysis; leaves open prospective validation before guiding care.
Background Dialysis patients have an exceedingly high mortality rate. Biomarkers may be useful tools in risk stratification of this population. We evaluated the prognostic value of high‐sensitivity cardiac troponin T (hs‐ cTnT ) and CRP (C‐reactive protein) in predicting adverse outcomes in stable hemodialysis and peritoneal dialysis ( PD ) patients. Variability in hs‐ cTnT was also examined. Methods and Results A retrospective cohort study included 574 dialysis patients (hemodialysis 347, PD 227). Outcomes examined included mortality and major adverse cardiovascular events, with median follow‐up of 3.5 years. hs‐ cTnT was an independent predictor of both outcomes in hemodialysis and PD patients. Increased risk only became significant when hs‐ cTnT reached quintile 3 (>49 ng/L). Area under the receiver operating curve analysis showed that the addition of hs‐ cTnT to clinical parameters significantly improved its prognostic performance for mortality in PD patients ( P =0.002). CRP was an independent predictor of both outcomes in PD patients only. Only CRP in the highest quintile (>16.8 mg/L) was associated with increased risk. hs‐ cTnT remained relatively stable for the whole follow‐up period for hemodialysis patients, whereas for PD patients, hs‐ cTnT increased by 23.63% in year 2 and 29.13% in year 3 compared with baseline ( P <0.001). Conclusions hs‐ cTnT and CRP are useful tools in predicting mortality and major adverse cardiovascular events in hemodialysis and PD patients. Given that hs‐ cTnT levels increase over time in PD patients, interval monitoring may be valuable for risk assessment. In contrast, hs‐ cTnT in hemodialysis patients has little interval change and progress monitoring is not indicated.
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Chen et al. (2018) conducted a cohort in End-stage kidney disease on hemodialysis or peritoneal dialysis (n=574). Elevated high-sensitivity cardiac troponin T (hs-cTnT quintile 5, ≥109 ng/L) vs. Lowest hs-cTnT quintile (≤31 ng/L) was evaluated on All-cause mortality (HR 3.67, 95% CI 1.98 to 6.82, p=<0.001). High-sensitivity cardiac troponin T in the highest quintile (≥109 ng/L) independently predicted all-cause mortality (HR 3.67, 95% CI 1.98-6.82; P<0.001) and MACE (HR 3.90; P<0.001) in dialysis patients.
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