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Updated: Jun 19, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
[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.
Introduction:
Introduction Patients with Chronic renal Disease (CRD) often have cardiovascular disease that is the main cause of morbidity and mortality. Oxidative stress and a subclinical inflammation are crucial factors in its development. The aim of this study was to asses the oxidation of the main molecular lines in patients with advanced renal disease without dialysis and to determinate the best biomarker to asses this stress.
Patients And Methods:
We performed an observational study to measure the most important oxidative biomarkers in 32 patients with stage 4 CRD (MDRD = 22.1 +/- 1.08 ml/min) compared with the values obtained in a control group. In peripheral lymphocytes we measured, the lipid peroxidation by Malondialdehyde (MDA) and F2 Isoprostanes in plasma; protein oxidation by glutathione oxidized/reduced ratio (GSSG/GSH) in peripheral lymphocytes and protein carbonyls in plasma and the oxidative damage in genetic material by modified nucleotide base 8-deoxiguanosina oxo -(8-oxo-dG), after isolating nuclear and mitochondrial DNA. We also studied the antioxidant defenses with superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione reductase (GSR) and catalase (CAT) in peripheral lymphocytes. We studied the correlation between oxidative stress and the renal function and oxidative stress and co-morbidity factors.
Results:
All biomarkers showed important differences in comparison with the control subjects. 821.89 +/- 300.47 ng/ml vs. 270 (95.66) * ng/ml (p < 0.000), MDA 0.11 (0.11) * vs. 0.7 +/- 0.31 nmol/mg prot (p <0.000). GSSG / GSH: 6.89 +/- 1.91 vs. 1.39 +/- 0.75 (p <0.000), protein carbonyls: 7.41 +/- 0.84 vs. 3.63 (1.12) *. Nuclear 8-oxo-dG 7.88 (2.32) vs. 2.96 (1.78) * mitochondrial 8-oxo-dG: 15.73 +/- 2.28 vs. 13.85 +/- 1.44 (p <0.05). The Antioxidant enzymes also showed differences. Nuclear 8-oxo-dG demonstrated an important relationship with the rest of biomarkers, homocysteine (r = 0.305, p <0.05), lipoprotein (a) (r = 0.375, p <0.01), mitochondrial 8-oxo-dG (r = 0.411, p <0.05), GSSH/GSH (r = 0.595, p <0.001) and protein carbonyls (r = 0.489, p <0.05). There was an inverse correlation with total protein (r = -0.247, p <0.01), GSH (r = -0.648, p <0.000), GSR (r = -0.563, p <0.001) and SOD (r = -0.497, p <0.000). We did not find any correlation between these parameters and renal function. The presence of diabetes or the treatment with statins did not showed significant differences. * Median (Interquartile range).
Conclusion:
There is an important oxidative stress in patients with advanced renal disease, probably established during early stages of disease. Of the studied parameters, the nuclear 8-oxo-dG is the best marker for oxidative stress in CRD.
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