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Serum HBsAg and HBcrAg is associated with inflammation in HBeAg-positive chronic hepatitis B patients
Jing Zhao1, Dandan Bian1,2, Hao Liao3,4
1Liver Disease Center, Beijing YouAn Hospital, Capital Medical University, Beijing, China.
Insights
Non-invasive biomarkers like HBsAg and HBcrAg, alongside AST, can effectively assess liver inflammation in chronic hepatitis B (CHB) patients, potentially replacing liver biopsy for diagnosis and grading.
Area of Science:
- Hepatology
- Virology
- Biomarker Discovery
Background:
- Liver inflammation is a key driver of fibrosis, cirrhosis, and hepatocellular carcinoma in chronic hepatitis B (CHB).
- Accurate, non-invasive biomarkers are needed to diagnose and grade liver necroinflammation, reducing reliance on liver biopsy.
Purpose of the Study:
- To investigate the correlation between serum biomarkers and liver inflammation grade in CHB patients.
- To evaluate the diagnostic performance of novel biomarkers for significant liver inflammation.
Main Methods:
- Ninety-four CHB patients received antiviral therapy (entecavir or adefovir).
- Serum HBV RNA, HBV DNA, HBsAg, HBcrAg, ALT, AST, and intrahepatic HBV DNA were measured.
- Liver inflammation was assessed by biopsy at baseline and 60 months, with regression defined as ≥1-grade decrease.
Main Results:
- In HBeAg-positive patients, HBsAg and HBcrAg negatively correlated with inflammation, while ALT and AST positively correlated.
- The combination of AST and HBsAg showed excellent diagnostic ability for significant inflammation (AUROC 0.896).
- After 60 months of treatment, liver inflammation significantly improved in nearly all patients, with no progression observed.
Conclusions:
- Serum HBsAg and HBcrAg, in addition to ALT and AST, correlate with liver inflammation grade in HBeAg-positive CHB patients before antiviral treatment.
- The combination of HBsAg and AST demonstrates strong diagnostic potential for significant liver inflammation.
- Antiviral therapy leads to significant amelioration of liver inflammation in CHB patients.
Backgrounds & Aims:
Liver inflammation is the main risk factor for developing liver fibrosis, cirrhosis, and even hepatocellular carcinoma in chronic hepatitis B (CHB) patients. To replace biopsy, additional non-invasive biomarkers to diagnose and grade liver necroinflammation are urgently required in clinical practice.
Method:
Ninety-four CHB patients, including 74 HBeAg-positive and 20 HBeAg-negative patients, were enrolled and started entecavir or adefovir therapy. Serum HBV RNA, HBV DNA, HBsAg, hepatitis B core-related antigen (HBcrAg), ALT and AST levels, as well as intrahepatic HBV DNA and cccDNA were measured at baseline and during treatment. Liver inflammation was assessed at baseline and month 60 by liver biopsy. Inflammation regression was defined as a ≥1-grade decrease according to the Scheuer scoring system.
Results:
In HBeAg-positive CHB patients, at baseline, serum HBsAg and HBcrAg levels negatively correlated with inflammation grade, while ALT and AST levels positively correlated with inflammation grade. AST plus HBsAg exhibited excellent diagnostic ability for significant inflammation with an AUROC of 0.896. After 60 months of antiviral treatment, almost all the patients' liver inflammation ameliorated to G1, and no patients had inflammation progression.
Conclusion:
Besides ALT and AST, serum HBsAg and HBcrAg correlated with inflammation grade in HBeAg-positive CHB patients before NAs treatment. Moreover, the combination of HBsAg and AST exhibited excellent diagnostic ability for significant inflammation.
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