Abstract
BACKGROUND: Hepatitis B core-related antigen (HBcrAg), a novel serum biomarker reflecting the activity of intrahepatic covalently closed circular DNA (cccDNA), has generated conflicting evidence regarding its clinical utility for predicting post-antiviral therapy relapse in chronic hepatitis B (CHB) patients. METHODS: We systematically analyzed 13 studies (15 cohorts, n = 1529 patients) from PubMed, Web of Science, Wanfang, and CNKI (through April 2025). A bivariate model evaluated HBcrAg's predictive performance for relapse outcomes, including virological relapse, clinical relapse, and hepatitis flares. RESULTS: HBcrAg demonstrated a pooled sensitivity of 0.81 (95% CI: 0.75-0.86) and specificity of 0.72 (95% CI: 0.67-0.76) for relapse prediction, with a diagnostic odds ratio of 10.66 (95% CI: 7.36-15.42) and summary AUC of 0.83 (95% CI: 0.80-0.86). Subgroup analysis identified threshold effects as the primary source of heterogeneity, which resolved (I(2) < 13%) after excluding studies with outlier cutoff values. Meta-regression established that HBcrAg's predictive value was unaffected by age, sex, hepatitis B e antigen status, or detection methods (p > 0.05). CONCLUSIONS: HBcrAg is validated as a robust non-invasive biomarker to optimize treatment cessation strategies, with high sensitivity providing strong negative predictive value in CHB populations. Future research should prioritize multi-marker models to enhance prediction accuracy.