Biomarkers of Uremic Cardiotoxicity

Bojan Stopic1, Sandra Dragicevic2, Branislava Medic-Brkic3

  • 1Clinical Department for Nephrology, Zvezdara University Medical Center, Dimitrija Tucovica 161, 11000 Belgrade, Serbia.

Toxins
|September 26, 2021
PubMed

Insights

Cardiovascular disease risk increases with chronic kidney disease (CKD). Serum albumin, urea, and interventricular septum thickness are key predictors of cardiovascular events in CKD patients.

Area of Science:

  • Nephrology
  • Cardiology
  • Biomarker Research

Background:

  • Cardiovascular (CV) disease is a major complication of chronic kidney disease (CKD).
  • Early detection of CV risk in CKD patients is crucial.
  • Novel cardiotoxicity biomarkers are being investigated.

Purpose of the Study:

  • To identify novel biomarkers for early detection of cardiotoxicity in CKD patients.
  • To analyze potential biomarkers including inflammation, oxidative stress, acute kidney injury, and microRNAs.
  • To assess CV risk predictors in non-dialysis-dependent (NDD) and dialysis-dependent (DD) CKD populations.

Main Methods:

  • Prospective cohort study of 87 CKD patients (NDD and DD) followed for 18 months.
  • Recorded newly occurred CV events.
  • Utilized Cox regression analysis to identify significant predictors of CV outcome.

Main Results:

  • Serum albumin, urea, interventricular septum thickness diameter (IVST), calcium antagonist use, and erythropoiesis-stimulating agent use were significant predictors of CV outcome.
  • Biomarkers of inflammation, oxidative stress, acute kidney injury (IL-18, CRP, ferritin, IMA, SOD, NGAL, KIM-1), and miR-133a did not show significant differences related to CV events or left ventricular hypertrophy.
  • Serum albumin, urea, IVST, calcium antagonist, and erythropoiesis-stimulating agents are associated with CV events in CKD.

Conclusions:

  • Serum albumin, urea, IVST, and specific medications are associated with CV events in CKD patients.
  • Current inflammation, oxidative stress, and acute kidney injury biomarkers are not significantly different in CKD patients with or without CV events.
  • Further research is needed to discover reliable cardiotoxicity biomarkers in CKD.

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