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PAGE-B incorporating moderate HBV DNA levels predicts risk of HCC among patients entering into HBeAg-positive chronic hepatitis B

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dc.contributor.author김승업-
dc.contributor.author안상훈-
dc.date.accessioned2024-03-22T06:26:19Z-
dc.date.available2024-03-22T06:26:19Z-
dc.date.issued2024-01-
dc.identifier.issn0168-8278-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/198548-
dc.description.abstractBackground & aims: Recent studies reported that moderate HBV DNA levels are significantly associated with hepatocellular carcinoma (HCC) risk in hepatitis B e antigen (HBeAg)-positive, non-cirrhotic patients with chronic hepatitis B (CHB). We aimed to develop and validate a new risk score to predict HCC development using baseline moderate HBV DNA levels in patients entering into HBeAg-positive CHB from chronic infection. Methods: This multicenter cohort study recruited 3,585 HBeAg-positive, non-cirrhotic patients who started antiviral treatment with entecavir or tenofovir disoproxil fumarate at phase change into CHB from chronic infection in 23 tertiary university-affiliated hospitals of South Korea (2012-2020). A new HCC risk score (PAGED-B) was developed (training cohort, n = 2,367) based on multivariable Cox models. Internal validation using bootstrap sampling and external validation (validation cohort, n = 1,218) were performed. Results: Sixty (1.7%) patients developed HCC (median follow-up, 5.4 years). In the training cohort, age, gender, platelets, diabetes and moderate HBV DNA levels (5.00-7.99 log10 IU/ml) were independently associated with HCC development; the PAGED-B score (based on these five predictors) showed a time-dependent AUROC of 0.81 for the prediction of HCC development at 5 years. In the validation cohort, the AUROC of PAGED-B was 0.85, significantly higher than for other risk scores (PAGE-B, mPAGE-B, CAMD, and REAL-B). When stratified by the PAGED-B score, the HCC risk was significantly higher in high-risk patients than in low-risk patients (sub-distribution hazard ratio = 8.43 in the training and 11.59 in the validation cohorts, all p <0.001). Conclusions: The newly established PAGED-B score may enable risk stratification for HCC at the time of transition into HBeAg-positive CHB. Impact and implications: In this study, we developed and validated a new risk score to predict hepatocellular carcinoma (HCC) development in patients entering into hepatitis B e antigen (HBeAg)-positive chronic hepatitis B (CHB) from chronic infection. The newly established PAGED-B score, which included baseline moderate HBV DNA levels (5-8 log10 IU/ml), improved on the predictive performance of prior risk scores. Based on a patient's age, gender, diabetic status, platelet count, and moderate DNA levels (5-8 log10 IU/ml) at the phase change into CHB from chronic infection, the PAGED-B score represents a reliable and easily available risk score to predict HCC development during the first 5 years of antiviral treatment in HBeAg-positive patients entering into CHB. With a scoring range from 0 to 12 points, the PAGED-B score significantly differentiated the 5-year HCC risk: low <7 points and high ≥7 points.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherElsevier-
dc.relation.isPartOfJOURNAL OF HEPATOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAntiviral Agents / therapeutic use-
dc.subject.MESHCarcinoma, Hepatocellular* / chemically induced-
dc.subject.MESHCarcinoma, Hepatocellular* / etiology-
dc.subject.MESHChild, Preschool-
dc.subject.MESHCohort Studies-
dc.subject.MESHDNA, Viral-
dc.subject.MESHHepatitis B e Antigens-
dc.subject.MESHHepatitis B virus / genetics-
dc.subject.MESHHepatitis B, Chronic* / complications-
dc.subject.MESHHepatitis B, Chronic* / drug therapy-
dc.subject.MESHHumans-
dc.subject.MESHLiver Neoplasms* / chemically induced-
dc.subject.MESHLiver Neoplasms* / etiology-
dc.subject.MESHPersistent Infection-
dc.subject.MESHRisk Factors-
dc.titlePAGE-B incorporating moderate HBV DNA levels predicts risk of HCC among patients entering into HBeAg-positive chronic hepatitis B-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorHo Soo Chun-
dc.contributor.googleauthorGeorge V Papatheodoridis-
dc.contributor.googleauthorMinjong Lee-
dc.contributor.googleauthorHye Ah Lee-
dc.contributor.googleauthorYeong Hwa Kim-
dc.contributor.googleauthorSeo Hyun Kim-
dc.contributor.googleauthorYun-Seo Oh-
dc.contributor.googleauthorSu Jin Park-
dc.contributor.googleauthorJihye Kim-
dc.contributor.googleauthorHan Ah Lee-
dc.contributor.googleauthorHwi Young Kim-
dc.contributor.googleauthorTae Hun Kim-
dc.contributor.googleauthorEileen L Yoon-
dc.contributor.googleauthorDae Won Jun-
dc.contributor.googleauthorSang Hoon Ahn-
dc.contributor.googleauthorVana Sypsa-
dc.contributor.googleauthorCihan Yurdaydin-
dc.contributor.googleauthorPietro Lampertico-
dc.contributor.googleauthorJose Luis Calleja-
dc.contributor.googleauthorHarry LA Janssen-
dc.contributor.googleauthorGeorge N Dalekos-
dc.contributor.googleauthorJohn Goulis-
dc.contributor.googleauthorThomas Berg-
dc.contributor.googleauthorMaria Buti-
dc.contributor.googleauthorSeung Up Kim-
dc.contributor.googleauthorYoon Jun Kim-
dc.identifier.doi10.1016/j.jhep.2023.09.011-
dc.contributor.localIdA00654-
dc.contributor.localIdA02226-
dc.relation.journalcodeJ01441-
dc.identifier.eissn1600-0641-
dc.identifier.pmid37734683-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0168827823050961-
dc.subject.keywordHBeAg-positive chronic hepatitis B-
dc.subject.keywordHBeAg-positive chronic infection-
dc.subject.keywordhepatocellular carcinoma-
dc.subject.keywordrisk prediction model-
dc.contributor.alternativeNameKim, Seung Up-
dc.contributor.affiliatedAuthor김승업-
dc.contributor.affiliatedAuthor안상훈-
dc.citation.volume80-
dc.citation.number1-
dc.citation.startPage20-
dc.citation.endPage30-
dc.identifier.bibliographicCitationJOURNAL OF HEPATOLOGY, Vol.80(1) : 20-30, 2024-01-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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