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Published on: October 2, 2020
Plasma concentrations of novel cardiac biomarkers before and after hemodialysis session
Thomas Mueller1, Alfons Gegenhuber2, Gert Kronabethleitner2
1Department of Laboratory Medicine, Konventhospital Barmherzige Brueder, Linz, Austria.
Insights
Cardiovascular biomarkers like NT-proBNP are elevated in chronic kidney disease patients undergoing hemodialysis. High-flux dialysis significantly reduces these biomarker levels, unlike low-flux dialysis.
Area of Science:
- Nephrology
- Cardiology
- Clinical Chemistry
Background:
- Biomarkers are crucial for assessing chronic kidney disease (CKD) severity and prognosis.
- Novel cardiovascular biomarkers may offer insights into the complications of CKD.
Purpose of the Study:
- To determine plasma concentrations of specific cardiovascular biomarkers in hemodialysis patients.
- To compare these concentrations against established upper reference limits (URL).
- To evaluate the impact of hemodialysis (low-flux vs. high-flux) on these biomarker levels.
Main Methods:
- Plasma levels of NT-proBNP, MR-proANP, MR-proADM, CT-proET-1, CT-proAVP (Copeptin), and sST2 were measured.
- Samples were collected from 28 patients before and after hemodialysis.
- Patients underwent either low-flux hemofiltration or high-flux hemodiafiltration.
Main Results:
- Pre-hemodialysis concentrations of NT-proBNP, MR-proANP, MR-proADM, CT-proET-1, and CT-proAVP exceeded their respective URLs.
- Soluble ST2 (sST2) levels were below the URL.
- High-flux dialysis significantly decreased NT-proBNP, MR-proANP, MR-proADM, CT-proET-1, and CT-proAVP levels post-session.
- Low-flux dialysis showed minimal or no significant reduction in these biomarker levels, with some increasing.
Conclusions:
- Investigated cardiovascular biomarkers are significantly elevated in chronic hemodialysis patients, except for sST2.
- High-flux hemodialysis effectively reduces elevated cardiovascular biomarker concentrations.
- Low-flux membranes are less effective in clearing these biomarkers during hemodialysis.
Objectives:
Biomarkers are useful for establishing disease severity or prognosis in patients with chronic kidney disease. The aim of our study was to determine the plasma concentrations of novel cardiovascular biomarkers in patients on chronic hemodialysis in the context of published upper reference limits (URL) of these biomarkers; and to compare the plasma concentrations of those same analytes before and after hemodialysis session.
Design And Methods:
Plasma concentrations of N-terminal pro-B-type natriuretic peptide (NT-proBNP), mid-regional pro-A-type natriuretic peptide (MR-proANP), mid-regional pro-adrenomedullin (MR-proADM), C-terminal pro-endothelin-1 (CT-proET-1), C-terminal pro-arginine vasopressin (CT-proAVP, also known as Copeptin) and soluble ST2 (sST2) were measured in 28 patients before and after dialysis session. Of the 28 patients with conventional hemodialysis, 24 had low-flux hemofiltration and 4 had high-flux hemodiafiltration.
Results:
Median plasma concentrations of the biomarkers obtained before hemodialysis were as follows: NT-proBNP, 11,307ng/L (URL, 500ng/L); MR-proANP, 778pmol/L (URL, 250pmol/L); MR-proADM, 2.57nmol/L (URL, 0.52nmol/L); median CT-proET-1, 252pmol/L (URL, 75pmol/L); median CT-proAVP, 142pmol/L (URL, 19pmol/L); and median sST2, 27ng/mL (URL, 50ng/mL). Median relative analyte changes after low-flux vs. high-flux dialysis compared to predialysis values were +19% vs. -43% for NT-proBNP; +7% vs. -45% for MR-proANP; -2% vs. -63% for MR-proADM; -19% vs. -61% for CT-proET-1; +13% vs. -64% for CT-proAVP; and +2% vs. +3% for sST2.
Conclusions:
Plasma concentrations of the investigated biomarkers were markedly increased in chronic hemodialysis patients (with the exception of sST2). After hemodialysis session, analyte concentrations (with the exception of sST2) decreased significantly using a high-flux membrane but not if using a low-flux membrane.
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