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Increased procollagen type I C-terminal peptide levels indicate diastolic dysfunction in end-stage renal disease
Chi-Ting Su1, Yen-Wen Liu, Jou-Wei Lin
1Division of Nephrology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Insights
Diastolic dysfunction in hemodialysis patients is linked to increased left ventricular filling pressures and cardiac fibrosis. Procollagen type I C-terminal peptide (PICP) may indicate diastolic dysfunction and elevated pressures.
Area of Science:
- Nephrology
- Cardiology
- Biomedical Engineering
Background:
- Cardiac dysfunction is prevalent in end-stage renal disease (ESRD) patients.
- Diastolic dysfunction is a common cardiac issue in ESRD patients undergoing hemodialysis.
Purpose of the Study:
- To investigate the factors determining diastolic dysfunction in ESRD patients on maintenance hemodialysis.
- To explore the relationship between cardiac fibrosis markers and diastolic dysfunction severity.
Main Methods:
- Doppler tissue imaging and 2D speckle-tracking echocardiography were used for strain analysis in asymptomatic ESRD patients.
- Blood markers including albumin, cardiac troponin T, and procollagen type I C-terminal peptide (PICP) were analyzed.
Main Results:
- All patients exhibited left ventricular (LV) diastolic dysfunction, with 87% having grade 1.
- Patients with an average E/e' ratio ≥ 13 had elevated PICP levels.
- PICP correlated significantly with cardiac troponin T, E/e' ratio, and systolic circumferential strain rate.
Conclusions:
- High average E/e' ratios in hemodialysis patients indicate increased LV filling pressure and cardiac fibrosis severity, preceding systolic dysfunction.
- PICP shows potential as an indicator for diastolic dysfunction and elevated LV filling pressure in this population.
Background:
Cardiac dysfunction is common among patients with end-stage renal disease. The aim of this study was to explore the determinants of diastolic dysfunction in patients with end-stage renal disease on maintenance hemodialysis.
Methods:
Patients with asymptomatic end-stage renal disease undergoing hemodialysis underwent Doppler tissue imaging analysis and two-dimensional speckle-tracking echocardiography with strain analysis. Blood studies included albumin, cardiac troponin T, and procollagen type I C-terminal peptide (PICP).
Results:
All enrolled patients had left ventricular (LV) diastolic dysfunction and were stratified into two groups by a cutoff value of 13 for the ratio of early transmitral flow velocity to the average early diastolic annular velocity (E/e'). Seventy-two of the enrolled patients (87%) had grade 1 diastolic dysfunction, and 11 patients (13%) had higher grades of diastolic dysfunction. The study population did not include a representative sample of patients with the pseudonormal or restrictive filling patterns of diastolic dysfunction. There were no significant differences in gender, age, LV geometric change, ejection fraction, global systolic longitudinal strain and strain rate, and prevalence of comorbidities between groups. Patients with average E/e' ≥ 13 had higher PICP, which was significantly correlated with cardiac troponin T, average E/e', and systolic circumferential strain rate. By multivariate regression analysis, average E/e' level was an independent factor of PICP level (P = .047).
Conclusions:
Hemodialysis patients with high average E/e' ratios showed increased levels of LV filling pressure and higher severity levels of cardiac fibrosis, which occurred before the development of systolic dysfunction. PICP was a potential indicator of diastolic dysfunction and increased LV filling pressure.
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