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HBeAg-positive CHB Patients with Indeterminate Phase Associated with a High Risk of Significant Fibrosis

Overview
Journal Virol J
Publisher Biomed Central
Specialty Microbiology
Date 2024 Nov 13
PMID 39538258
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Abstract

Background: The risk of liver fibrosis in HBeAg-positive chronic hepatitis B (CHB) patients with indeterminate phase is not well characterized. We aimed to compare the presence of liver fibrosis in HBeAg-positive CHB patients between indeterminate phase and immune-tolerant phase.

Methods: This multi-center, retrospective cohort study included 719 treatment-naïve HBeAg-positive CHB patients with normal alanine aminotransferase (ALT). Patients with HBV DNA > 10 IU/mL were categorized into immune-tolerant phase, whereas those with HBV DNA ≤ 10 IU/mL were classified into indeterminate phase. Significant liver fibrosis and cirrhosis were determined by APRI, FIB-4, transient elastography, or liver biopsy.

Results: The median age of patients was 33.0 years and 59.8% of patients were male. 81.5% and 18.5% of patients were in the immune-tolerant phase and indeterminate phase, respectively. The APRI (0.33 vs. 0.27, P < 0.001), FIB-4 (1.07 vs. 0.72, P < 0.001), and liver stiffness values (7.80 kPa vs. 5.65 kPa, P = 0.011) were higher in patients with indeterminate phase than those with immune-tolerant phase. Patients in the indeterminate phase had significantly higher proportions of significant fibrosis (27.1% vs. 11.3%, P < 0.001) and cirrhosis (14.3% vs. 3.2%, P < 0.001) compared to those in the immune-tolerant phase. In the multivariate analysis, indeterminate phase (OR 2.138, 95% CI 1.253, 3.649, P = 0.005) was associated with a higher risk of significant fibrosis, especially for patients aged ≥ 30 years.

Conclusion: HBeAg-positive CHB patients in the indeterminate phase had more severe liver fibrosis compared to those in the immune-tolerant phase.

Citing Articles

Serological and Molecular Characterization of the Hepatitis B Virus in Blood Donors in Maputo City, Mozambique.

Maquessene O, Laurindo O, Chambal L, Ismael N, Mabunda N Viruses. 2025; 17(1).

PMID: 39861883 PMC: 11768953. DOI: 10.3390/v17010094.

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