Occult Hepatitis B Virus Infection in Patients With Chronic Hepatitis C Treated With Antiviral Therapy

authors:

avatar Gian Paolo Caviglia 1 , avatar Maria Lorena Abate 1 , avatar Paola Manzini 2 , avatar Franca Danielle 2 , avatar Alessia Ciancio ORCID 3 , avatar Chiara Rosso 1 , avatar Antonella Olivero 1 , avatar Rinaldo Pellicano ORCID 3 , * , avatar Giovanni Antonio Touscoz ORCID 3 , avatar Antonina Smedile ORCID 3 , avatar Mario Rizzetto ORCID 3

Department of Internal Medicine, University of Turin, Italy
Blood Bank, San Giovanni Battista University Hospital (Molinette), Italy
Department of Gastroenterology and Hepatology, San Giovanni Battista University Hospital (Molinette), rinaldo_pellican@hotmail.com, Italy

How To Cite Caviglia G, Abate M, Manzini P, Danielle F, Ciancio A, et al. Occult Hepatitis B Virus Infection in Patients With Chronic Hepatitis C Treated With Antiviral Therapy. Hepat Mon. 2012;12(11):7292. https://doi.org/10.5812/hepatmon.7292.

Abstract

Background:

Occult hepatitis B virus infection (OBI) is defined as the presence of hepatitis B virus (HBV) DNA in the liver and/or in the serum of patients with negative results of hepatitis B s antigen (HBsAg) test with or without serological markers of previous viral exposure. The impact of OBI in patients with chronic hepatitis C (CHC) is still unclear.

Objectives:

The Aim of this study was to assess OBI prevalence and its potential implications on treatment outcome in a cohort of patients with CHC underwent standard antiviral therapy.

Patients and Methods:

Baseline serum samples from 137 HBsAg-negative CHC patients treated with pegylated-interferon and ribavirin (73 Responders/74 Non Responders),were retrospectively analyzed for HBV status.

Results:

Seventy-three patients (53.3%) showed markers of previous exposure to HBV. HBV DNA was detected in 2 of 137 serum samples (1.5%), both carrying HBV antibodies. Liver biopsies and post-therapy sera were available for 35 patients (12 Responders/23 Non Responders). HBV DNA sequences were found in 13 of 35 specimens (37.1%), all of patients with HBV DNA negativity in basal and post-therapy serum samples. Among OBI-positive patients, 5 (38.5%) carried serological markers of HBV infection. Regarding therapy outcome, in the OBI-positive group there were 5 of 13 (38.5%) sustained virological responders (SVR) compared to 7 of 22 (31.8%) in the OBI-negative one.

Conclusions:

Despite the high prevalence rate of liver HBV DNA in patients with CHC, SVR was not affected by occult HBV infection.

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