Low membrane protein sulfhydrils but not G6PD deficiency predict ribavirin-induced hemolysis in hepatitis C
Open Access
- 26 April 2004
- journal article
- clinical trial
- Published by Wolters Kluwer Health in Hepatology
- Vol. 39 (5) , 1248-1255
- https://doi.org/10.1002/hep.20208
Abstract
Hemolysis is a frequent adverse effect of ribavirin (RBV). It has been suggested that oxidative stress plays a role, but mechanisms and predictive risk factors for severe forms remain unknown. Markers of redox status were determined in erythrocytes of 34 patients with hepatitis C—four of them with glucose-6-phosphate-dehydrogenase (G6PD) deficiency—before and during treatment with RBV and interferon (IFN) and were compared with 10 healthy control subjects. In addition, erythrocytes were incubated with RBV, and the effects of dipyridamole (DPD), diethylmaleate (DEM), and glutathione ester (GSHE) were studied in vitro. Of the 30 patients without G6PD deficiency who were treated with RBV and IFN-α, five developed major hemolysis (Δ hemoglobin > 6 g/dL) and 25 developed minor hemolysis (Δ hemoglobin < 2.5 g/dL). Patients with major hemolysis had lower median pretreatment values of membrane protein sulfhydrils than patients with minor hemolysis (28.4 vs. 36.7 nmol/mg, P < .001). Erythrocytes of G6PD-deficient patients were not more susceptible to RBV-induced hemolysis. In in vitro incubations of erythrocytes, DEM enhanced the RBV-induced decrease of glutathione, protein sulfhydrils, and osmotic resistance. Supplementation of GSHE and DPD prevented the RBV-induced decrease in osmotic resistance, adenosyl triphosphate (ATP), and 2,3-diphosphoglycerate (DPG), the loss of glutathione and protein sulfhydrils, and the formation of thiobarbituric acid reactive substances (TBARs). In conclusion, the data indicate that low membrane protein sulfhydrils prior to therapy but not G6PD deficiency are predictive of RBV-induced major hemolysis. In vitro, GSHE and DPD reduce the RBV-associated oxidative stress in erythrocytes and prevent the increase in osmotic fragility, suggesting that these compounds might decrease the risk of hemolysis in patients. (Hepatology 2004;39:1248-1255.)Keywords
Funding Information
- Roche Pharmaceuticals, Basel, Switzerland
- Swiss National Science Foundation (32-66377.01, 32-66378.01)
This publication has 24 references indexed in Scilit:
- Ribavirin dose modification based on renal function is necessary to reduce hemolysis in liver transplant patients with hepatitis C virus infectionLiver Transplantation, 2002
- Peginterferon Alfa-2a plus Ribavirin for Chronic Hepatitis C Virus InfectionNew England Journal of Medicine, 2002
- Factors influencing ribavirin-induced hemolysisJournal of Hepatology, 2001
- Hemolytic anemia induced by ribavirin therapy in patients with chronic hepatitis C virus infection: Role of membrane oxidative damageHepatology, 2000
- Randomised trial of interferon α2b plus ribavirin for 48 weeks or for 24 weeks versus interferon α2b plus placebo for 48 weeks for treatment of chronic infection with hepatitis C virusPublished by Elsevier ,1998
- Ribavirin uptake by human erythrocytes and the involvement of nitrobenzylthioinosine‐sensitive (es)‐nucleoside transportersBritish Journal of Pharmacology, 1998
- Oxidation of circulating proteins in alcoholics: role of acetaldehyde and xanthine oxidaseJournal of Hepatology, 1996
- The metabolism of ribavirin in erythrocytes and nucleated cellsInternational Journal of Biochemistry, 1990
- Menadione-induced bleb formation in hepatocytes is associated with the oxidation of thiol groups in actinArchives of Biochemistry and Biophysics, 1988
- Ribavirin disposition in high-risk patients for acquired immunodeficiency syndromeClinical Pharmacology & Therapeutics, 1987