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Baseline and on-treatment HBcrAg levels as predictors of HBeAg seroconversion in chronic hepatitis B patients treated with antivirals

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dc.contributor.authorHwang, Soo Young-
dc.contributor.authorYoo, Sung Hwan-
dc.contributor.authorChang, Hye Young-
dc.contributor.authorKim, Sora-
dc.contributor.authorLee, Jung Il-
dc.contributor.authorLee, Kwan Sik-
dc.contributor.authorCho, Young Youn-
dc.contributor.authorKim, Hyung Joon-
dc.contributor.authorLee, Hyun Woong-
dc.date.accessioned2023-10-18T02:40:37Z-
dc.date.available2023-10-18T02:40:37Z-
dc.date.issued2023-01-
dc.identifier.issn1352-0504-
dc.identifier.issn1365-2893-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/68095-
dc.description.abstractHBeAg seroconversion is an important treatment endpoint. We aimed to identify predictors of seroconversion using serum HBsAg and hepatitis B core-related antigen (HBcrAg) in HBeAg-positive patients treated with nucleos(t)ide analogs (NAs). Data and samples from 70 HBeAg-positive patients treated with entecavir or tenofovir between January 2007 and December 2017 were retrospectively analysed. The mean follow-up period was 11 years. The predictive power for HBeAg seroconversion of HBcrAg levels at baseline and 2 years after antiviral therapy was determined using receiver operating curve analysis. Twenty-one patients (30%) achieved HBeAg seroconversion at a mean of 28 (range, 12-84) months after antiviral treatment. The median baseline HBcrAg and HBsAg levels were 6.9(5.7-7.0) vs. 5.8(5.5-6.5) log(10)U/mL (p = .006), 4.9(4.5-5.1) vs. 4.5(4.1-5.0) log(10)IU/mL (p = .044) in the no seroconversion group and seroconversion group, respectively. In the multivariate analysis, the serum HBcrAg levels at baseline and 2 years after antiviral therapy were predictive factors for HBeAg seroconversion ([HR]; 0.326; [CI], 0.111-0.958; p = .042 and HR, 0.4555; CI, 0.211-0.984; p = .045). HBcrAg levels <= 6.5log(10)U/mL at baseline and <= 5.3log(10)U/mL at 2 years after antiviral therapy had sensitivities of 53.1% and 69.8%, specificities of 95.2% and 70.6%, positive predictive values of 82.6% and 50.0%, and negative predictive values of 82.6% and 84.5%, respectively, with AUROCs of 0.712 (95%CI, 0.596-0.830) and 0.745 (95%CI, 0.599-0.891) for predicting HBeAg seroconversion. In chronic hepatitis B patients treated with NAs, HBcrAg levels <= 6.5log(10)U/mL at baseline and <= 5.3log(10)U/mL at 2 years after antiviral therapy were useful predictive factors of HBeAg seroconversion.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherWILEY-
dc.titleBaseline and on-treatment HBcrAg levels as predictors of HBeAg seroconversion in chronic hepatitis B patients treated with antivirals-
dc.typeArticle-
dc.identifier.doi10.1111/jvh.13765-
dc.identifier.bibliographicCitationJOURNAL OF VIRAL HEPATITIS, v.30, no.1, pp 39 - 45-
dc.description.isOpenAccessN-
dc.identifier.wosid000881872700001-
dc.identifier.scopusid2-s2.0-85142084056-
dc.citation.endPage45-
dc.citation.number1-
dc.citation.startPage39-
dc.citation.titleJOURNAL OF VIRAL HEPATITIS-
dc.citation.volume30-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthorhepatitis B-
dc.subject.keywordAuthorhepatitis B core-related antigen-
dc.subject.keywordAuthorhepatitis B e antigen seroconversion-
dc.subject.keywordAuthorhepatitis B surface antigen-
dc.subject.keywordAuthornucleos(t)ide analog-
dc.subject.keywordPlusCORE-RELATED ANTIGEN-
dc.subject.keywordPlusCLOSED CIRCULAR DNA-
dc.subject.keywordPlusNUCLEOS(T)IDE ANALOGS-
dc.subject.keywordPlusVIRUS GENOTYPES-
dc.subject.keywordPlusSURFACE-ANTIGEN-
dc.subject.keywordPlusMARKER-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusMANAGEMENT-
dc.subject.keywordPlusINFECTION-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalResearchAreaInfectious Diseases-
dc.relation.journalResearchAreaVirology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryInfectious Diseases-
dc.relation.journalWebOfScienceCategoryVirology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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