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Hepatitis C infection in hemodialysis patients: Protective against oxidative stress?
Insights
Hepatitis C virus (HCV) infection in hemodialysis patients is linked to reduced oxidative stress markers. This study found lower plasma oxidative load in HCV-infected individuals undergoing dialysis.
Area of Science:
- Nephrology
- Hepatology
- Clinical Biochemistry
Background:
- Hepatitis C virus (HCV) infection elevates morbidity and mortality in hemodialysis patients.
- Hemodialysis patients face increased risk of oxidative stress.
- Understanding the interplay between HCV and oxidative stress is crucial for this vulnerable population.
Purpose of the Study:
- To investigate the association between HCV infection and oxidative stress indicators.
- To evaluate plasma oxidative status in hemodialysis patients awaiting transplantation.
Main Methods:
- Studied 73 hemodialysis patients (26 with HCV) using spectrophotometric methods.
- Measured plasma superoxide dismutase (SOD), glutathione peroxidase (GPX), and malonyldialdehyde (MDA).
- Retrospectively analyzed laboratory values and clinical findings, excluding chronic inflammation or advanced liver failure.
Main Results:
- HCV-infected patients exhibited significantly lower levels of malonyldialdehyde (MDA), albumin, total cholesterol, triglyceride, predialysis creatinine, and phosphorus.
- Antioxidative indicators (SOD, GPX) were higher in the HCV group, though not statistically significant.
- HCV infection was associated with a decreased plasma oxidative load.
Conclusions:
- Hepatitis C virus infection in hemodialysis patients correlates with a reduced plasma oxidative load.
- Further research is needed to elucidate the mechanisms behind this observed association.
Abstract:
Hepatitis C virus (HCV) infection is a common problem that increases morbidity and mortality in hemodialysis patients. These patients are also at risk of increased oxidative stress. The aim of this study was to evaluate possible interactions between HCV infection and oxidative stress indicators in a group of hemodialysis patients awaiting transplantation. We evaluated 73 patients (29 women, 44 men; ages, 49.3 +/- 13.3 years; dialysis duration, 81.7 +/- 48.8 months; Kt/V > or = 1.3). Indicators of plasma oxidative status were monitored at the beginning of a clinically stable hemodialysis session. Measurements were performed for plasma superoxide dismutase (SOD), glutathione peroxidase (GPX), and malonyldialdehyde (MDA) by spectrophotometric methods. We retrospectively recorded the prior year's monthly laboratory values for alanine aminotransferase (ALT), C-reactive protein (CRP), albumin, lipids, homocysteine, Lp(a), calcium, phosphorus, intact parathyroid hormone, and predialysis blood urea nitrogen (BUN) creatinine, as well as clinical findings of body mass index and pre- and postdialysis blood pressures. We excluded patients with chronic inflammation (mean CRP levels > or = 10 mg/L) or HCV infection of duration <12 months or clinically advanced liver failure. Twenty-six patients had HCV. The sex distribution, mean age, and dialysis duration were similar between groups. HCV-infected patients showed significantly lower levels of MDA, albumin, total cholesterol, triglyceride, predialysis creatinine, and phosphorus. Antioxidative indicator levels were also higher in the HCV group, but they were not statistically significant. In conclusion, HCV infection in dialysis patients is associated with decreased levels of plasma oxidative load.
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