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Prediction for HBsAg seroconversion in children with chronic hepatitis B
Yan-Wei Zhong1, Yan-Min Shi2, Fang Chu2
1Senior Department of Hepatology, the Fifth Medical Center of Chinese PLA General Hospital, Xisihuan Mid-Road No.100, 100039, Beijing, China. zhongyanwei@126.com.
Insights
Predicting Hepatitis B surface antigen (HBsAg) seroconversion in children with chronic hepatitis B (CHB) is possible using baseline serum HBsAg levels or intrahepatic covalently closed circular DNA (cccDNA). This aids clinicians in selecting effective treatment strategies.
Area of Science:
- Hepatology
- Virology
- Pediatric Infectious Diseases
Background:
- Chronic hepatitis B (CHB) affects children globally, necessitating predictive markers for treatment.
- Hepatitis B surface antigen (HBsAg) seroconversion is a key treatment goal in CHB management.
- Accurate prediction of HBsAg seroconversion aids in optimizing therapeutic strategies for pediatric CHB patients.
Purpose of the Study:
- To establish a predictive model for HBsAg seroconversion in children with CHB.
- To identify key factors influencing HBsAg seroconversion.
- To assist clinicians in selecting appropriate treatment strategies and resource allocation.
Main Methods:
- Sixty-three children with HBeAg-positive CHB (aged 1-17 years) treated with interferon-alpha (IFNα) were analyzed.
- Patients were categorized into seroconversion (S) and non-seroconversion (NS) groups based on week 48 outcomes.
- Multivariate COX regression and Area Under the Receiver Operating Characteristic Curve (AUROC) were employed to identify predictors and assess model performance.
Main Results:
- Age, baseline intrahepatic cccDNA, and serum HBsAg levels were independent predictors of HBsAg seroconversion.
- Intrahepatic cccDNA showed a positive correlation with serum HBsAg levels (r=0.464, p=0.000).
- AUROC values for intrahepatic cccDNA and baseline HBsAg were 0.83 and 0.77, respectively, demonstrating good predictive capability.
Conclusions:
- Baseline serum HBsAg levels and intrahepatic cccDNA are reliable predictors of HBsAg seroconversion in pediatric CHB.
- The developed prediction index can guide clinical decision-making for CHB treatment.
- Improved prediction can lead to more personalized therapies and efficient use of medical resources.
Background:
To establish a prediction of HBsAg seroconversion in children with chronic hepatitis B (CHB), so as to help clinicians to choose therapeutic strategy.
Methods:
A total of 63 children with HBeAg-positive CHB aged 1 to 17 years, who admitted to the fifth medical center of Chinese PLA general hospital and treated with interferon α (IFNα) 48 weeks were enrolled, the clinical data were measured. Based on the results of HBsAg seroconversion (HBsAg < 0.05 IU/mL and anti-HBsAg > 10 IU/L) at week 48, the patients were divided into HBsAg seroconversion (S) group and non-HBsAg seroconversion (NS) group. Multivariate COX regression was used to identify the impact factors associated with HBsAg seroconversion. A novel prediction index was established and the area under the receiver operating characteristic curve (AUROC) was used to assess the prediction for HBsAg seroconversion.
Results:
The 63 patients were divided into S group (20.6%, 13/63) and NS group (79.4%, 50/63). Univariate and multivariate analysis identified age, baseline intrahepatic cccDNA and serum HBsAg levels were independent impact factors for HBsAg seroconversion. Intrahepatic cccDNA was positively correlated with serum HBsAg (r = 0.464, p = 0.000). AUROC of HBV cccDNA was 0.83 (95% CI 0.71 to 0.95) and AUROC of baseline HBsAg was 0.77 (95% CI 0.61 to 0.92). Intrahepatic cccDNA ≤ 0.08 log10 copies/106 cell is regarded as cutoff value, the positive predictive value(PPV) and negative predictive value(NPV) for HBsAg seroconversion were 86.8% and 60.0%, respectively, with a sensitivity of 92.0% and specificity of 56.2%. HBsAg ≤ 3.68 log10 IU/mL is used as cut off value, the PPV and NPV for HBsAg seroconversion were 91.2% and 56.3%, respectively; the sensitivity and specificity was 86.0% of 69.2%, respectively. There was no statistical difference between them for predicting HBsAg seroconversion (p = 0.146).
Conclusions:
HBsAg seroconversion can be predicted by the baseline serum HBsAg or intrahepatic cccDNA in children with CHB. Using the index, clinicians can choose more reasonable therapeutic strategy and reduce the waste of medical resources.
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