Natural History and Disease Progression in Chinese Chronic Hepatitis B Patients in Immune-tolerant Phase
Overview
Authors
Affiliations
Unlabelled: In view of the findings that high hepatitis B virus (HBV) deoxyribonucleic acid (DNA) is associated with increased risk of chronic hepatitis B (CHB)-related complications, disease progression in CHB patients in the immune-tolerant phase is uncertain. We evaluated disease progression in 57 immune-tolerant CHB patients with high HBV DNA. Each subject underwent an initial liver biopsy. In those who remained in the immune-tolerant phase, a follow-up liver biopsy was performed after 5 years of follow-up. Patients who developed elevated serum alanine aminotransferase (ALT) levels were discontinued from the study after a follow-up liver biopsy. Disease progression was defined as a 1-point increase in fibrosis stage. Initial liver biopsies showed the median fibrosis stage of the study patients was 1 (range 0-1). By the end of follow-up, 9 of the 57 patients (15.8%) had developed elevated serum ALT. In those who remained in the immune-tolerant phase, follow-up fibrosis stage was comparable with the initial fibrosis stage (P = 0.58). However, disease progression was greater in patients who developed elevated serum ALT when compared with those who remained in the immune-tolerant phase (5 of 9 vs. 3 of 48, respectively, P = 0.001). The median rate of fibrosis progression of patients who remained in the immune-tolerant phase was lower than that of patients with high serum ALT (0 U/year [range -0.40-0.20 U/year] versus 0.21 U/year [range 0-1.11 U/year], respectively, P = 0.04).
Conclusion: CHB patients in the immune-tolerant phase have mild disease. In those who remained in the immune-tolerant phase in the present study, disease progression was minimal. However, immune-tolerant patients who progressed to the immune clearance phase often faced disease progression.
Pak K, Sachar R, Saab S Dig Dis Sci. 2025; .
PMID: 39979574 DOI: 10.1007/s10620-025-08909-z.
Probability analysis of hepatocellular carcinoma in hepatitis patients in the gray zone.
Zhang J, Yu S, Zhu K, Li S, Huang Y Front Med (Lausanne). 2025; 11():1464981.
PMID: 39776842 PMC: 11703914. DOI: 10.3389/fmed.2024.1464981.
Liang H, Wang H, Liang M, Zhang X, Dai M, Li H Clin Exp Med. 2025; 25(1):32.
PMID: 39775320 PMC: 11711149. DOI: 10.1007/s10238-024-01537-3.
Existing problems and new advice on stage criteria of natural history for chronic hepatitis B.
Xing T BMC Infect Dis. 2025; 25(1):17.
PMID: 39754052 PMC: 11699759. DOI: 10.1186/s12879-024-10408-x.
Li Y, Zhu Y, Gao D, Pan Y, Wang J, Zhang S Virol J. 2024; 21(1):287.
PMID: 39538258 PMC: 11562367. DOI: 10.1186/s12985-024-02561-1.