Serum HBsAg and HBcrAg is associated with inflammation in HBeAg-positive chronic hepatitis B patients

Front Cell Infect Microbiol. 2023 Mar 31:13:1083912. doi: 10.3389/fcimb.2023.1083912. eCollection 2023.

Abstract

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.

Keywords: HBcrAg; HBsAg; chronic hepatitis B; inflammation; nucleos(t)ide analogues.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / therapeutic use
  • Biomarkers
  • DNA, Circular / therapeutic use
  • DNA, Viral / genetics
  • Hepatitis B Core Antigens / genetics
  • Hepatitis B Surface Antigens / genetics
  • Hepatitis B e Antigens / therapeutic use
  • Hepatitis B virus / genetics
  • Hepatitis B, Chronic* / complications
  • Hepatitis B, Chronic* / drug therapy
  • Humans
  • Inflammation / drug therapy
  • Liver Cirrhosis / diagnosis
  • Liver Neoplasms*

Substances

  • Hepatitis B Surface Antigens
  • Hepatitis B e Antigens
  • DNA, Viral
  • DNA, Circular
  • Hepatitis B Core Antigens
  • Antiviral Agents
  • Biomarkers

Grants and funding

This study was supported in part by National Science and Technology Key Project on “Major Infectious Diseases such as HIV/AIDS, Viral Hepatitis Prevention and Treatment“ (2017ZX10302201-004, 2017ZX10202203-006); Beijing Municipal Administration of Hospitals Clinical medicine Development of special funding support (ZYLX202125); Beijing Natural Science Foundation (No. 7222093); High-level public health technical talents construction project of Beijing Municipal Health Commission (Academic Leader -02-14); and National Key Research and Development Program of Ministry of Science and Technology, (2022YFC2304400).