HBsAg profiles in patients receiving peginterferon alfa-2a plus ribavirin for the treatment of dual chronic infection with hepatitis B and C viruses

Ming Lung Yu, Chuan Mo Lee, Wan Long Chuang, Sheng Nan Lu, Chia Yen Dai, Jee Fu Huang, Zu Yau Lin, Tsung I. Hu, Chien Hung Chen, Chao Hung, Jin Houng Wang, Chi Ling Chen, Jia Horng Kao, Ming Yang Lai, Chen Hua Liu, Tung Hung Su, Shun Sheng Wu, Li Ying Liao, Hsing Tao Kuo, You Chen ChaoShui Yi Tung, Sien Sing Yang, Pei Jer Chen, Chun Jen Liu*, Ding Shinn Chen

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

43 Scopus citations

Abstract

Background. With use of peginterferon alfa-2a and ribavirin combination therapy in patients with dual chronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infection, 11.2% of patients achieved clearance of hepatitis B surface antigen (HBsAg) at 6 months after treatment; however, reactivation of HBV DNA was observed in 36.3%. We investigated the predictive potential of HBsAg quantification. Methods. HBsAg quantification was performed in 120 e antigen-negative patients dually infected with HBV and hepatitis C virus and treated with peginterferon alfa-2a/ribavirin for 48 weeks (HCV genotype 1; n = 74) or 24 weeks (HCV genotype 2/3; n = 46). HBsAg was quantified at baseline, week 4, week 12, end of treatment, and 24 weeks after treatment. Results. The baseline median serum HBsAg level was 120 IU/mL and decreased gradually during treatment. Low baseline HBsAg was significantly associated with HBsAg clearance (40% for HBsAg level ≤20 IU/mL vs 2.2% for HBsAg level >20 IU/mL; P< .05). A decrease in HBsAg level from baseline to week 12 of 50% was associated with a reduced likelihood of HBV DNA reactivation in patients with baseline undetectable serum HBV DNA (positive predictive value, 89.5%). Conclusions. HBsAg quantification appears to be a useful indicator of posttreatment outcome in patients dually infected with HBV and hepatitis C virus.

Original languageEnglish
Pages (from-to)86-92
Number of pages7
JournalJournal of Infectious Diseases
Volume202
Issue number1
DOIs
StatePublished - 01 07 2010

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