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Example clinical scenario

A 42-year-old man, of eastern European origin, attends an emergency department and is diagnosed with chronic hepatitis B. He consumes 10 units of alcohol per week and has a BMI of 26. He is not known to have any medical issues. Laboratory testing returns serum alanine transaminase (ALT) of 54 IU/L (normal 30–50IU/L). He is hepatitis B surface antigen positive, e-antigen positive, IgM anti-HBc negative and with detectable viral load of 12,000IU/mL. Anti-HDV is negative.

What do you need to know?

  • HBV genotyping is not necessary in the initial evaluation, although it may be useful for selecting patients to be treated with pegylated interferon-alpha (PegIFN-α) and offering prognostic information for the probability of response to PegIFN-α therapy and the risk of hepatocellular carcinoma (HCC). Only patients with mild to moderate fibrosis (and possibly those with compensated advanced chronic liver disease) should be considered for PegIFN-α therapy.
  • HBV genotypes A and B are associated with higher rates of HBV surface antigen loss (rates of 35%–54% and 21%–27% respectively) than genotypes C and D in response to PegIFN-α therapy.
  • PegIFN-α in HBV genotype C achieves a 19%–32% sustained virological response (SVR) rate.
  • PegIFN-α is less effective in HBV genotypes D or E (7%–15% and 20% SVR rate respectively).

What do you need to do?

If it is felt that it would be beneficial to know which HBV genotype the patient has to guide treatment decisions (usually after discussion at the hepatitis operational delivery network multidisciplinary meeting), then you should complete HBV genotyping tests as per your local virology policy.

Resources

For clinicians

References:

For patients

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  • Last reviewed: 28/02/2025
  • Next review due: 28/02/2026
  • Authors: Dr Robert A D Scott
  • Reviewers: Professor Guruprasad P Aithal, Professor William L Irving