Abstract

Background: Intravenous application of iron preparations which is a routine treatment of anemia in hemodialysis patients with end-stage renal disease can lead to iron overload in the body. Redox-active iron can catalyze the formation of hydroxyl radicals and initiation of lipid peroxidation, increase oxidative stress and speed up the development of complications in these patients. Objective: In this study, we determined the markers of lipid peroxidation, protein oxidation and antioxidant enzyme activities (superoxide dismutase, glutathione peroxidase, glutathione S-transferase) in serum of patients with end-stage renal disease on hemodialysis, who had received repeated treatment of iron supplementation. Patients and Methods: The study included 29 patients undergoing regular hemodialysis treatment. These patients were divided into three groups according to the serum ferritin levels: group I (serum ferritin between 100 and 300 mg/L); group II (serum ferritin between 301 and 600 mg/L), and group III (serum ferritin above 601 mg/L). Results: The serum of patients with the highest concentration of serum ferritin and iron contained significantly higher level of lipid peroxidation products, total hydroperoxides and malondialdehyde and advanced oxidation protein products and the lowest concentration of sulfhydryl groups, reduced glutathione and total antioxidant capacity. Conclusion: Based on the obtained results, it can be concluded that iron supplementation in hemodialysis patients and consequently body iron overload of exacerbated oxidative stress have already been present in these patients.

Highlights

  • Numerous researches have shown that in patients with end-stage renal disease (ESRD), production of reactive oxygen species (ROS) and subsequent oxidative stress increase [1]

  • The treatment of patients with ESRD—hemodialysis, contributes to the reduction of antioxidant levels and development of oxidative stress in several ways: 1) activation of phagocytic oxidative metabolism by the dialysis membrane causes chronic inflammation [2], 2) hemoincopatibility of the dialysis system contributes to production of oxygen radicals during dialysis [1], 3) direct peroxidation of lipids on dialysis membranes [3], 4) hydrosoluble antioxidants and substances with small molecular weight are lost through highly permeable dialysis membrane [4]

  • Aim In this study, we determined the markers of lipid peroxidation, protein oxidation and antioxidant enzyme activities (superoxide dismutase (SOD EC 1.15.1.1), glutathione peroxidase (GPx, EC 1.11.1.9), glutathione Stransferase (GST, EC 2.5.1.18) in serum of patients with end-stage renal disease on hemodialysis, who had received repeated treatment of iron supplementation

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Summary

Introduction

Numerous researches have shown that in patients with end-stage renal disease (ESRD), production of reactive oxygen species (ROS) and subsequent oxidative stress increase [1]. Intravenous application of iron preparations which is a routine treatment of anemia in hemodialysis patients with end-stage renal disease can lead to iron overload in the body. Redox-active iron can catalyze the formation of hydroxyl radicals and initiation of lipid peroxidation, increase oxidative stress and speed up the development of complications in these patients. Objective: In this study, we determined the markers of lipid peroxidation, protein oxidation and antioxidant enzyme activities (superoxide dismutase, glutathione peroxidase, glutathione S-transferase) in serum of patients with end-stage renal disease on hemodialysis, who had received repeated treatment of iron supplementation. Conclusion: Based on the obtained results, it can be concluded that iron supplementation in hemodialysis patients and body iron overload of exacerbated oxidative stress have already been present in these patients

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