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Published on: September 25, 2019
Response to interferon-alpha in chronic hepatitis B patients with and without precore mutant strain and effects on
Sila Cetin Akhan1, Zerrin Yulugkural, Haluk Vahaboglu
1Kocaeli University Medical Faculty, Infectious Diseases and Clinical Microbiology, Umuttepe, Kocaeli, Turkey. silacetin@superonline.com
Insights
Hepatitis B surface antigen (HBsAg) titers can predict treatment response in chronic hepatitis B patients, particularly those who are HBeAg-negative. This finding aids in personalizing interferon-alpha therapy for better outcomes.
Area of Science:
- Hepatology
- Virology
- Immunology
Background:
- Chronic hepatitis B (CHB) impacts 400 million globally, leading to significant morbidity and mortality.
- Hepatitis B virus (HBV) DNA is often detected post-HBsAg clearance in various bodily tissues.
- Predicting treatment response in CHB is crucial for effective management.
Purpose of the Study:
- To evaluate HBsAg titers, quantitative HBV DNA, and ALT levels for predicting interferon-alpha (IFN-alpha) treatment response.
- To assess the impact of precore mutants on HBsAg titers and IFN-alpha therapy response.
Main Methods:
- Study included 21 HBeAg-positive, 38 HBeAg-negative CHB patients, and 47 healthy carriers.
- Patients had no prior IFN-alpha therapy and no cirrhosis on liver biopsy.
- HBsAg titers were monitored over a 6-month interval.
Main Results:
- A statistically significant decrease in HBsAg titers was observed in HBeAg-negative patients (p=0.0001).
- HBsAg titer decrease was not statistically significant in HBeAg-positive patients (p=0.192) or healthy carriers (p=0.236).
Conclusions:
- HBsAg titer is a potential predictor of primary responders and nonresponders to IFN-alpha therapy.
- This predictive value is particularly relevant for HBeAg-negative CHB patients.
- Further research can refine HBsAg titer monitoring for personalized CHB treatment strategies.
Background:
Chronic hepatitis B (CHB) affects 400 million people worldwide and is a major cause of morbidity and mortality. It is known that HBV DNA sequences were detected after the clearance of serum hepatitis B surface antigen (HBsAg) often in serum, liver and peripheral blood mononuclear cells. The objectives of our study were to evaluate the previous measurements of HBsAg titers versus. quantitative hepatitis B virus (HBV) DNA and ALT measurements in order to predict the nonresponse and response in interferon-alpha (IFN-alpha)-treated HBeAg-positive and HBeAg-negative chronic HBV patients.
Methods:
We investigate whether the presence of precore mutant affects the response to IFN-alpha therapy and on the titer of HBsAg or not. Twenty-one HBeAg-positive (group 1), 38 HBeAg-negative (group 2), and 47 healthy inactive carriers (group 3) made up this study. Liver biopsy showed chronic hepatitis, there was no cirrhosis and none of the patients had IFN-alpha therapy before.
Results:
The decrease in HBsAg titers was found as statistically not significant in groups 1 (p = 0.192) and 3 (p = 0.236) and statistically significant in group 2 (p = 0.0001) within a 6-month interval.
Conclusion:
HBsAg titer may be a factor to predict the primary responders and nonresponders specially in HBeAg-negative patients.
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