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Hepatitis B Surface Antigen Loss and Improved Clinical Outcomes in Asians with Chronic Hepatitis B Virus Infection
Wallis Lau1,2,3, Myriam Drysdale4, Eleonora Morais4
1Department of Pharmacology and Pharmacy, The University of Hong Kong, Hong Kong, China.
Insights
Hepatitis B surface antigen (HBsAg) loss significantly reduces the risk of liver disease, cancer, and death in chronic hepatitis B patients. This functional cure marker indicates improved long-term clinical outcomes.
Area of Science:
- Hepatology
- Virology
- Public Health
Background:
- Chronic hepatitis B virus (HBV) infection presents a significant global health burden.
- Hepatitis B surface antigen (HBsAg) loss is a critical indicator of functional cure in HBV treatment.
- Further research is needed to understand the clinical impact of HBsAg loss.
Purpose of the Study:
- To investigate the association between HBsAg loss and clinical outcomes in patients with chronic HBV infection.
- To evaluate the impact of HBsAg loss on compensated cirrhosis, decompensated liver disease (DLD), hepatocellular carcinoma (HCC), and all-cause mortality (ACM).
- To assess changes in healthcare resource utilization following HBsAg loss.
Main Methods:
- A population-based cohort study utilizing electronic health records from Hong Kong (2005-2019).
- Inclusion of 71,077 patients with chronic HBV infection.
- Application of a marginal structural model with inverse probability weighting to adjust for confounders and estimate hazard ratios (HRs).
Main Results:
- HBsAg loss was associated with a significant reduction in the risk of DLD (74%), HCC (66%), and ACM (26%).
- The hazard ratio for compensated cirrhosis was 0.57 (95% CI 0.30-1.14).
- Each additional month of HBsAg loss correlated with decreased risk of HCC and ACM; healthcare resource utilization decreased post-HBsAg loss.
Conclusions:
- HBsAg loss is strongly associated with reduced risks of DLD, HCC, and ACM in chronic HBV patients.
- The findings support HBsAg loss as a key marker for favorable long-term clinical outcomes in chronic hepatitis B management.
- This study highlights the importance of monitoring HBsAg status for assessing treatment efficacy and patient prognosis.
Background And Aims:
Chronic hepatitis B virus (HBV) infection accounts for substantial disease burden and mortality due to liver complications. Hepatitis B surface antigen (HBsAg) loss is a key component of functional cure when assessing treatment efficacy. However, the impact of HBsAg loss on clinical outcomes deserves further exploration.
Methods:
This population-based cohort study used electronic health record data from a territory-wide database in Hong Kong to identify patients with chronic HBV infection (2005-2019). The association between HBsAg loss and outcomes was assessed: compensated cirrhosis, decompensated liver disease (DLD), hepatocellular carcinoma (HCC), and all-cause mortality (ACM). A marginal structural model using inverse probability weighting was used to estimate hazard ratios (HRs; 95% confidence interval [CI]) adjusted for time-fixed and time-varying confounders. Health-care resource utilization before and after loss was evaluated.
Results:
The study population comprised 71,077 patients accruing 348,379 person-years; 1639 (2.3%) experienced HBsAg loss, which occurred with a mean (standard deviation) of 74.63 (37.5) months after chronic HBV index date. HBsAg loss was associated with a reduced risk of DLD (74%; HR 0.26 [95% CI 0.08-0.83]), HCC (66%; 0.34 [0.19-0.61]), and ACM (26%; 0.74 [0.57-0.97]). The HR for compensated cirrhosis was 0.57 (0.30-1.14). Each additional month of HBsAg loss was associated with decreased risk of HCC and ACM. Of those experiencing HBsAg loss, cumulative probability of persistence at 24 and 60 months was 99% and 97%, respectively. Hospital admission, inpatient days, and drug prescribing were higher before HBsAg loss versus 6, 12, and 24 months post-HBsAg loss.
Conclusion:
In this large population-based study with extended follow-up in Hong Kong, HBsAg loss was associated with reduced risk of DLD, HCC, and ACM.
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