Acute hepatitis B in patients with or without underlying chronic HCV infection

Summary Background and aim Acute hepatitis B course may be significantly modified by underlying chronic hepatitis C. The aim of this study was to compare clinical and virological characteristics of acute hepatitis B in patients with or without chronic hepatitis C virus (HCV) infection. Materials and...

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Veröffentlicht in:The Journal of infection 2008-08, Vol.57 (2), p.152-157
Hauptverfasser: Biliotti, E, Kondili, L.A, Furlan, C, Ferretti, G, Zacharia, S, De Angelis, M, Guidi, S, Gusman, N, Taliani, G
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Sprache:eng
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Zusammenfassung:Summary Background and aim Acute hepatitis B course may be significantly modified by underlying chronic hepatitis C. The aim of this study was to compare clinical and virological characteristics of acute hepatitis B in patients with or without chronic hepatitis C virus (HCV) infection. Materials and methods Twenty-seven patients with symptomatic acute hepatitis B were enrolled: 14 with underlying chronic HCV (Group A) and 13, matched by age and gender, with single hepatitis B (Group B). All patients were followed-up until HBsAg negativization. Results Group A patients were HCV-RNA-negative on hospital admission and all but one remained negative during follow-up. HBeAg tested positive in 92.9% and 84.6% of Groups A and B patients, respectively. ALT, bilirubin, prothrombin time values and HBsAg titer were similar in both groups. Nevertheless, lower mean HBV-DNA levels ( p = 0.03), a shorter duration of HBsAg positivity ( p < 0.01) and of symptoms before ALT peak ( p = 0.014), and significantly lower peak ALT values ( p = 0.03) were observed in Group A compared to Group B patients. Conclusions Acute HBV infection suppressed HCV replication. Conversely, the underlying HCV infection exerted a modulatory effect on HBV replication which influenced the course, though not the outcome, of the acute disease. Although acute hepatitis B showed a mild clinical course in both groups of patients, HBV vaccination should be suggested to risk subjects.
ISSN:0163-4453
1532-2742
DOI:10.1016/j.jinf.2008.04.006