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      Low Serum Hepatitis B Surface Antigen Level Predicts Compensated Cirrhosis Caused by Chronic Hepatitis B in HBeAg Positive Patients in East China

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          Abstract

          Backgrounds:

          Serum hepatitis B surface antigen (HBsAg) levels are associated with fibrosis in patients with chronic hepatitis B (CHB) infection.

          Objectives:

          The aim of our study was to evaluate serum HBsAg level as a biomarker for compensated cirrhosis in hepatitis B e antigen (HBeAg) positive CHB patients.

          Patients and Methods:

          Two-hundred and one HBeAg-positive Chinese CHB patients with or without cirrhosis were enrolled in this retrospective study. Cirrhosis was diagnosed based on liver biopsy. Furthermore, patients with decompensated cirrhosis were excluded. A statistical analysis was performed regarding the association between serum HBsAg level and compensated cirrhosis.

          Results:

          Patients with compensated cirrhosis had a significantly lower mean serum HBsAg level compared to those without cirrhosis (3.27 Log 10 IU/mL VS 4.17 Log 10 IU/mL, P < 0.001). Furthermore, examining the correlation with compensated cirrhosis revealed that lower level of serum HBsAg was a significant factor in multivariate analysis. The area under the receiver operating characteristics curve of serum HBsAg was 0.856 for compensated cirrhosis. A positive predictive value of 66.2% and negative predictive value of 90.7% were obtained with a cut-off value of < 3.60 Log 10 IU/mL (4000 IU/mL) of serum HBsAg. Moreover, the rate of compensated cirrhosis increased to 75.0% after combining with APRI > 2.

          Conclusions:

          In HBeAg positive CHB patients, low serum HBsAg level is a useful predictor of compensated cirrhosis.

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          Most cited references29

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          EASL Clinical Practice Guidelines: management of chronic hepatitis B.

          (2009)
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            Asian-Pacific consensus statement on the management of chronic hepatitis B: a 2008 update

            Large amounts of new data on the natural history and treatment of chronic hepatitis B virus (HBV) infection have become available since 2005. These include long-term follow-up studies in large community-based cohorts or asymptomatic subjects with chronic HBV infection, further studies on the role of HBV genotype/naturally occurring HBV mutations, treatment of drug resistance and new therapies. In addition, Pegylated interferon α2a, entecavir and telbivudine have been approved globally. To update HBV management guidelines, relevant new data were reviewed and assessed by experts from the region, and the significance of the reported findings were discussed and debated. The earlier “Asian-Pacific consensus statement on the management of chronic hepatitis B” was revised accordingly. The key terms used in the statement were also defined. The new guidelines include general management, special indications for liver biopsy in patients with persistently normal alanine aminotransferase, time to start or stop drug therapy, choice of drug to initiate therapy, when and how to monitor the patients during and after stopping drug therapy. Recommendations on the therapy of patients in special circumstances, including women in childbearing age, patients with antiviral drug resistance, concurrent viral infection, hepatic decompensation, patients receiving immune-suppressive medications or chemotherapy and patients in the setting of liver transplantation, are also included.
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              • Article: not found

              Classification of chronic hepatitis: diagnosis, grading and staging.

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                Author and article information

                Journal
                Hepat Mon
                Hepat Mon
                10.5812/hepatmon
                Kowsar
                Hepatitis Monthly
                Kowsar
                1735-143X
                1735-3408
                30 August 2015
                August 2015
                : 15
                : 8
                : e29183
                Affiliations
                [1 ]Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China
                [2 ]Department of Infectious Diseases, Jing’An District Centre, Shanghai Hospital, Fudan University, Shanghai, China
                [3 ]Department of Liver Diseases, Xixi Hospital of Hangzhou, Zhejiang Chinese Medical University, Hangzhou, China
                Author notes
                [* ]Corresponding Authors: Ji-Ming Zhang, Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China. Tel: +86-2152887963, Fax: +86-2152886140, E-mail: jmzhang@ 123456fudan.edu.cn ; Ri-Cheng Mao, Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China. Tel: +86-2152887963, Fax: +86-2152886140, E-mail: richengmao@ 123456gmail.com
                Article
                10.5812/hepatmon.29183
                4546813
                d04e00fe-deac-4517-9980-58e67d103bdc
                Copyright © 2015, Kowsar Corp.

                This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License ( http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

                History
                : 12 April 2015
                : 27 May 2015
                : 07 July 2015
                Categories
                Research Article

                Infectious disease & Microbiology
                hepatitis b surface antigens,liver cirrhosis,hepatitis b e antigens,hepatitis b,chronic

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