Study of oxidative stress in patients with advanced renal disease and undergoing either hemodialysis or peritoneal dialysis

Oxidative stress (OS) is directly involved in the formation of atheroma plaque and has been shown to be present since the early stages of Chronic Kidney Disease (CKD); however, the net role that dialytica techniques may play in OS process is yet to be determined. We studied three groups: hemodialysi...

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Veröffentlicht in:Clinical nephrology 2013-09, Vol.80 (3), p.177-186
Hauptverfasser: Puchades, Maria J, Saez, Guillermo, Muñoz, M Carmen, Gonzalez, Miguel, Torregrosa, Isidro, Juan, Isabel, Miguel, Alfonso
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container_end_page 186
container_issue 3
container_start_page 177
container_title Clinical nephrology
container_volume 80
creator Puchades, Maria J
Saez, Guillermo
Muñoz, M Carmen
Gonzalez, Miguel
Torregrosa, Isidro
Juan, Isabel
Miguel, Alfonso
description Oxidative stress (OS) is directly involved in the formation of atheroma plaque and has been shown to be present since the early stages of Chronic Kidney Disease (CKD); however, the net role that dialytica techniques may play in OS process is yet to be determined. We studied three groups: hemodialysis (HD, n = 30), peritoneal dialysis (PD, n = 31), predialysis (pre-D, n = 32), and one control group (C, n = 67). Using highresolution liquid chromatography columns (HPLC), the superoxide dismutase (SOD), glutathione oxidized/reduced ratio (GSSG/GSH), and nuclear, as well as mitochondrial 8-oxo-dG (8-oxo-dG mit) were measured in lymphocytes. Protein carbonyls and F2-isoprostanes were measured in plasma. The antioxidant enzyme activity was evaluated by a spectrophotometric assay of catalase, glutathione peroxidase (GPX), glutathione reductase (GSR), and superoxide dismutase (SOD). Compared to the control group, all groups had significantly higher levels of products derived from molecular oxidation with a significant decrease in antioxidant enzymes. Patients in the pre-D group showed higher values for most of the oxidized molecules. The PD group showed a better oxidative balance, with no significant differences in levels of mitochondrial 8-oxo-dG when compared to the control group. We speculated that the better control of OS observed in patients receiving PD might be explained by the fact that this technique is more biocompatible, and this might help reduce the risk of cardiovascular events.
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subjects Adult
Aged
Biomarkers - blood
Case-Control Studies
Catalase - blood
Chi-Square Distribution
Chromatography, High Pressure Liquid
Cross-Sectional Studies
Deoxyguanosine - analogs & derivatives
Deoxyguanosine - blood
DNA Damage
F2-Isoprostanes - blood
Female
Glutathione - blood
Glutathione Peroxidase - blood
Glutathione Reductase - blood
Humans
Kidney Diseases - blood
Kidney Diseases - therapy
Linear Models
Lipid Peroxidation
Male
Middle Aged
Multivariate Analysis
Oxidative Stress
Peritoneal Dialysis
Protein Carbonylation
Renal Dialysis
Superoxide Dismutase - blood
Treatment Outcome
Up-Regulation
title Study of oxidative stress in patients with advanced renal disease and undergoing either hemodialysis or peritoneal dialysis
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