[Study of oxidative stress in advanced kidney disease]

M J Puchades Montesa1, M A González Rico, M A Solís Salguero

  • 1Servicio de Nefrología, Hospital Clinico Universitario de Valencia, Valencia, Spain. chuspuchades@gmail.com

Insights

Patients with advanced chronic renal disease (CRD) experience significant oxidative stress, a key factor in cardiovascular complications. Nuclear 8-oxo-deoxyguanosine (8-oxo-dG) emerged as the most reliable biomarker for assessing this stress in CRD patients.

Area of Science:

  • Biochemistry
  • Nephrology
  • Oxidative Stress Research

Context:

  • Cardiovascular disease is a major cause of mortality in patients with Chronic Renal Disease (CRD).
  • Oxidative stress and subclinical inflammation are implicated in the development of cardiovascular disease in CRD.
  • This study investigates oxidative stress markers in non-dialyzed patients with advanced CRD.

Purpose:

  • To assess oxidative stress by measuring key molecular oxidation markers in patients with advanced CRD.
  • To identify the most effective biomarker for quantifying oxidative stress in this patient population.
  • To explore correlations between oxidative stress markers, renal function, and comorbidities.

Summary:

  • Patients with stage 4 CRD exhibited significantly elevated levels of lipid peroxidation (MDA, F2 Isoprostanes), protein oxidation (GSSG/GSH ratio, protein carbonyls), and DNA damage (8-oxo-dG) compared to controls.
  • Nuclear 8-oxo-dG showed significant correlations with various oxidative stress markers and antioxidant defenses.
  • No significant correlation was found between oxidative stress markers and renal function, diabetes, or statin use.

Impact:

  • Highlights the substantial oxidative stress burden in advanced CRD, likely originating in earlier disease stages.
  • Identifies nuclear 8-oxo-dG as a superior biomarker for monitoring oxidative stress in CRD.
  • Provides insights into the complex interplay of oxidative stress and disease progression in CRD, informing potential therapeutic targets.
Abstract

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