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.
Abstract