Digestive Diseases and Sciences

, Volume 55, Issue 10, pp 2727–2734

Hepatitis B e Antigen Seroconversion: A Critical Event in Chronic Hepatitis B Virus Infection

  • Yun-Fan Liaw
  • George K. K. Lau
  • Jia-Horng Kao
  • Edward Gane
Review

Abstract

Background

Replication of hepatitis B virus (HBV) is the primary driver of disease progression and clinical outcomes in patients with chronic hepatitis B (CHB), but other factors, such as hepatitis B e antigen (HBeAg) status, also influence disease course. The importance of HBeAg seroconversion is underscored by current CHB treatment guidelines that recommend limiting the duration of antiviral therapy in HBeAg-positive patients who achieve seroconversion.

Aims

A 2-day meeting of leading hepatologists with extensive experience managing patients with CHB in the Asia–Pacific region was held with the overall goals of reviewing and evaluating (1) available data on the relationship between HBeAg seroconversion and clinical outcomes for patients with HBeAg-positive CHB, and (2) the ways in which seroconversion should influence patient management.

Conclusions

It was agreed that HBeAg seroconversion is an important serologic end point for patients with CHB and that achieving this goal should be an important consideration in treatment selection. Patients with HBeAg-positive CHB should consider pegylated interferon if they are aged <40 years (especially women), have lower HBV DNA levels, can afford this treatment, and have a lifestyle that would support adherence to injection therapy. Alternatively, nucleos(t)ide analogs are recommended in patients with alanine aminotransferase levels ≥2 × the upper limit of normal, HBV DNA levels <9 log10 IU/ml, and compensated CHB. Entecavir, telbivudine, and tenofovir may be used as first-line therapy; they can be administered as a finite therapeutic course in HBeAg-positive patients who seroconvert. Telbivudine and tenofovir should be considered in women of child-bearing potential.

Keywords

Hepatitis B Hepatitis B e antigen seroconversion Oral nucleos(t)ide therapy Pegylated interferon 

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Copyright information

© Springer Science+Business Media, LLC 2010

Authors and Affiliations

  • Yun-Fan Liaw
    • 1
  • George K. K. Lau
    • 2
  • Jia-Horng Kao
    • 3
  • Edward Gane
    • 4
  1. 1.Liver Research UnitChang Gung Memorial Hospital and Chang Gung University College of MedicineTaipeiTaiwan
  2. 2.Clinical Trial Center, LKS Faculty of MedicineThe University of Hong Kong, Humanity and Health GI and Liver ClinicHong KongChina
  3. 3.Hepatitis Research Center National Taiwan University HospitalTaipeiTaiwan
  4. 4.New Zealand Liver Transplant UnitAuckland City HospitalAucklandNew Zealand

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