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Updated: Jun 1, 2026

Real-Time Polymerase Chain Reaction-Based Detection and Quantification of Hepatitis B Virus DNA
Published on: December 15, 2023
The change of the quantitative HBsAg level during the natural course of chronic hepatitis B
Yu J Kim1, Hyun C Cho, Moon S Choi
1Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Insights
Hepatitis B e antigen (HBeAg) levels vary across chronic hepatitis B (CHB) phases and correlate with hepatitis B virus (HBV) DNA, aiding in understanding CHB progression.
Area of Science:
- Hepatology
- Virology
- Immunology
Background:
- Limited data exists on hepatitis B surface antigen (HBsAg) levels and their relationship with serum hepatitis B virus (HBV) DNA in chronic hepatitis B (CHB).
- Understanding these correlations is crucial for characterizing CHB phases and pathogenesis.
Purpose of the Study:
- To delineate HBsAg levels across different phases of CHB.
- To investigate the correlation between HBsAg and serum HBV DNA levels in treatment-naïve CHB patients.
Main Methods:
- Retrospective cross-sectional study of 645 treatment-naïve Korean CHB patients.
- Patients categorized into immune tolerance (IT), HBeAg-positive hepatitis (EPH), inactive carrier (IC), and HBeAg-negative hepatitis (ENH) phases.
- Baseline HBsAg and HBV DNA levels were quantified.
Main Results:
- Significant differences in mean HBsAg titres were observed across CHB phases (P<0.001).
- HBsAg and HBV DNA showed a significant positive correlation overall (r=0.693, P<0.001) and in IT, EPH, and IC groups, but not in the ENH group.
- Age and cirrhosis status were negatively correlated with HBsAg levels.
Conclusions:
- HBsAg levels exhibit significant variation across CHB phases.
- HBsAg correlates with HBV DNA in the immune tolerance, HBeAg-positive hepatitis, and inactive carrier phases.
- These findings enhance the understanding of CHB natural history and disease mechanisms.
Background:
There is insufficient information about HBsAg levels and their correlation with serum hepatitis B virus (HBV) DNA in chronic hepatitis B (CHB).
Aims:
We aimed to describe HBsAg levels during various phases of CHB and to investigate the correlation with serum HBV DNA levels.
Methods:
A total of 645 treatment-naïve Korean CHB patients were included in this retrospective cross-sectional study. They were categorized into immune tolerance (IT, n=56), HBeAg-positive hepatitis (EPH, n=150), inactive carrier (IC, n=274) and HBeAg-negative hepatitis (ENH, n=165). The baseline HBsAg and HBV DNA levels were measured.
Results:
The mean HBsAg titres (log IU/ml) differed (P<0.001): IT 4.29, EPH 3.64, IC 2.05 and ENH 3.23. In 645 patients, HBsAg and HBV DNA showed a significant correlation (r=0.693, P<0.001), and this was also observed in the IT, EPH and IC groups (r=0.664, r=0.541, r=0.505, respectively, all P<0.001), but not in the ENH group (r=0.093, P=0.321). Age had a negative correlation with HBsAg (r=-0.451, P<0.001). The cirrhotic patients had a significantly lower HBsAg level than the non-cirrhotic patients (2.41 ± 1.36 vs. 3.02 ± 1.21 log IU/ml, P<0.001).
Conclusions:
The HBsAg level varied significantly in different phases of CHB and was correlated with HBV DNA during the IT, EPH and IC phases. These findings can provide additional information to understand the natural course and pathogenesis of CHB.
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