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Low membrane protein sulfhydrils but not G6PD deficiency predict ribavirin‐induced hemolysis in hepatitis C
Author(s) -
Grattagliano Ignazio,
Russmann Stefan,
Palmieri Vincenzo O.,
Jüni Peter,
Bihl Florian,
Portincasa Piero,
Palasciano Giuseppe,
Lauterburg Bernhard H.
Publication year - 2004
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.20208
Subject(s) - ribavirin , hemolysis , medicine , virology , hepatitis c , chronic hepatitis , virus
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. (H EPATOLOGY 2004;39:1248–1255.)