Evidence map›Paper›PMID 42438905›Full record

ArticleThe Korean journal of internal medicine2026

Hepatitis B core-related antigen as a multifaceted biomarker in chronic hepatitis B: implications for immune activity and hepatocellular carcinoma prediction.

Kwon Yong Tak, Seok Hwan Kim, Myeong Jun Song

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Article in The Korean journal of internal medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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3 authors.

Kwon Yong TakDepartment of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Seok Hwan KimDepartment of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Myeong Jun SongDepartment of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea. mjsong95@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsHepatitis B core-related antigen (HBcrAg) reflects both serum hepatitis B virus (HBV) DNA and intrahepatic covalently closed circular DNA activity, offering potential advantages over conventional biomarkers in monitoring chronic hepatitis B (CHB). This study evaluated the clinical utility of HBcrAg across immune phases and its prognostic value for hepatocellular carcinoma (HCC).

methodsIn this retrospective study, 281 CHB patients from Daejeon St. Mary's Hospital (September 2022-July 2024) were classified into HBV phases. HBcrAg was quantified using the ultrasensitive iTACT-HBcrAg assay. HBcrAg level was compared across HBV phases, HCC presence, and patient characteristics.

resultsHBcrAg levels varied significantly across immune phases, with an AUC of 0.97 for HBeAg(+) IA vs. IT, and 0.83 for HBeAg(-) IA vs. II. In HBeAg(-) IA, HBcrAg ≥ 3.8 LogU/mL was associated with higher HCC prevalence at AUC 0.69, while in HBeAg(+) IA, ≥ 4.9 LogU/mL was the optimal cut-off at AUC 0.71. In HBeAg(-) II, HBcrAg < 3.8 LogU/mL was linked to the absence of HCC. HBcrAg correlated inversely with age (r = -0.31, p < 0.0001), while the relationship with fibrosis severity differed according to HBeAg status. In multivariate analysis, HBcrAg remained independently associated with HCC (OR 1.64, p = 0.002). Residual HBcrAg positivity was observed in patients with HBsAg loss.

conclusionHBcrAg is a robust biomarker capturing both virologic and immunologic activity in CHB, with additional prognostic value for HCC, particularly in IA phases. It may complement or surpass conventional markers in phase classification and risk stratification.

Indexed as

Carcinoma, HepatocellularHepatitis B, ChronicHepatitis B Core AntigensLiver NeoplasmsAdultBiomarkersDNA, ViralFemaleHepatitis B e AntigensHepatitis B virusHumansMaleMiddle AgedPredictive Value of TestsPrognosisRetrospective StudiesBiomarkersDNA, ViralHepatitis B Core AntigensHepatitis B e AntigensBiomarkersCarcinoma, hepatocellularHepatitis B, chronicHepatitis B e antigensViral load

Identifiers

PMID42438905
PMCPMC13358814

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