Biomarkers of cardiovascular remodeling in patients on peritoneal dialysis

Damir Rebić1, Senija Rašić, Amina Valjevac

  • 1Clinic for Nephrology, University of Sarajevo Clinical Center, Sarajevo, Bosnia and Herzegovina.

Insights

Peritoneal dialysis (PD) treatment led to decreased endothelin-1 (ET-1) and increased nitric oxide (NO) levels. These changes were linked to improved cardiovascular remodeling in PD patients.

Area of Science:

  • Nephrology
  • Cardiovascular Medicine
  • Biochemistry

Background:

  • Cardiovascular complications are a major concern for patients undergoing peritoneal dialysis (PD).
  • Endothelin-1 (ET-1) and nitric oxide (NO) play crucial roles in regulating vascular tone and cardiovascular remodeling.
  • Understanding their dynamics during PD is essential for managing cardiovascular risk.

Purpose of the Study:

  • To measure serum ET-1 and NO levels before and after 1 year of PD.
  • To assess the association between ET-1, NO, and cardiovascular remodeling parameters (echocardiography, carotid artery ultrasound).
  • To evaluate the influence of dialysis adequacy and residual renal function (RRF) on cardiovascular remodeling.

Main Methods:

  • A cohort of 40 PD patients was studied.
  • Serum ET-1 and NO concentrations were measured at baseline and after 12 months.
  • Echocardiography and common carotid artery (CCA) ultrasound were performed to assess cardiovascular parameters.

Main Results:

  • PD treatment significantly decreased ET-1 and increased NO levels (p < 0.01).
  • Significant reductions in left ventricular mass index (LVMI), CCA intima-media thickness (IMT), and plaque score were observed after 12 months (p < 0.001).
  • Dialysis adequacy and RRF were significantly associated with improvements in LVMI and CCA IMT.

Conclusions:

  • PD treatment favorably alters ET-1 and NO levels.
  • Both ET-1 and NO are independently related to cardiovascular remodeling in PD patients.
  • Dialysis adequacy and RRF are important factors influencing cardiovascular adaptation during PD.
Abstract

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