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Published on: October 12, 2017
Cardiac troponin T and malondialdehyde modified plasma lipids in haemodialysis patients
Benjamin Scott1, An Deman, Patrick Peeters
1Department of Nephrology, Academisch Ziekenhuis Vrije Universiteit Brussel, Belgium.
Insights
Cardiac troponin T (cTnT) elevation in end-stage renal disease (ESRD) patients on haemodialysis predicts poor prognosis. This increase is linked to oxidative stress, inflammation, and uraemia, indicating subclinical myocardial damage.
Area of Science:
- Nephrology
- Cardiology
- Biochemistry
Background:
- End-stage renal disease (ESRD) patients on haemodialysis exhibit high mortality.
- Cardiac troponin T (cTnT) is a known predictor of outcomes in this population.
- Investigating causes of cTnT elevation and its link to oxidative stress is crucial.
Purpose of the Study:
- To explore the causes of elevated cardiac troponin T (cTnT) in haemodialysis patients.
- To examine the relationship between cTnT and oxidative stress markers.
- To assess the prognostic value of cTnT in ESRD patients.
Main Methods:
- Studied 71 haemodialysis patients, measuring cTnT, malondialdehyde (MDA), and other biochemical markers.
- Performed serial measurements of cTnT and MDA over two weeks.
- Utilized transthoracic echocardiography in 49 patients to assess cardiac structure and function.
Main Results:
- 40.8% of patients had elevated cTnT.
- Higher cTnT levels correlated significantly with increased MDA, C-reactive protein (CRP), and pre-dialysis urea.
- cTnT, MDA, CRP, and age were independent predictors of survival.
Conclusions:
- Elevated cTnT is a significant predictor of poor prognosis in ESRD patients.
- cTnT elevation is associated with oxidative stress, inflammation, and uraemia.
- Subclinical myocardial damage, potentially from endothelial dysfunction, is suggested by the lack of specific echocardiographic findings.
Background:
In patients with end-stage renal disease (ESRD), treated with haemodialysis, a high overall mortality is observed. A previous study showed that cardiac troponin T (cTnT) is a strong independent predictor of outcome in this population. In this study we investigated possible causes of cTnT increase and its relationship with a marker of oxidative stress.
Methods:
In a group of 71 haemodialysis patients (36 male, 35 female, mean age 68.7+/-1.5 years) we determined cTnT and compared its presence with several biochemical parameters and with malondialdehyde (MDA), which is an indicator of oxidative stress. None of the patients suffered an acute coronary event during the observation period. Three measurements of cTnT and MDA were performed with a 2-week interval. Forty-nine patients underwent a transthoracic echocardiography.
Results:
Twenty-nine patients (or 40.8%) had a positive cTnT determination (defined as cTnT >/=0.10 ng/ml). cTnT positive patients had significantly higher levels of MDA (P=0.0125), C-reactive protein (CRP) (P=0.04) and pre-dialysis urea (P=0.04). Regression analysis showed that both pre-dialysis urea and MDA independently influenced cTnT. No correlation was found with age, dialysis adequacy, post-dialysis urea, total cholesterol, white blood cell count, fibrinogen or any of the echocardiographical parameters. Presence of heart failure, diabetes or use of medication could not discriminate between cTnT positive and cTnT negative patients. MDA levels correlated positively with time on haemodialysis (P=0.0021). Echocardiography showed left ventricular hypertrophy in 88% of the examined patients and impaired wall motion in 35%. Patients with clinical signs of heart failure had a lower ejection fraction and worse wall motion score index. No correlation existed between echocardiographic findings and cTnT or MDA. Survival was independently predicted by cTnT (P=0.0025), MDA (P=0.0007), CRP (P=0.006) and age (P=0.0143). Patients with both cTnT and CRP increase had a survival of <50% at 1 year, compared with 90% in patients with both cTnT and CRP within the normal range and 80% when either CRP or cTnT was increased (chi(2)=12.127; P=0.0023).
Conclusions:
This study confirms that the presence of cTnT predicts prognosis in ESRD. The presence of cTnT is linked to oxidative stress, inflammation and uraemia. The absence of specific findings on EKG and echocardiography points towards subclinical myocardial damage caused by endothelial disturbances.
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