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Extremely low risk of hepatocellular carcinoma development in patients with chronic hepatitis B in immune-tolerant phase

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dc.contributor.author박준용-
dc.contributor.author이관식-
dc.contributor.author이정일-
dc.contributor.author이현웅-
dc.contributor.author김승업-
dc.contributor.author김도영-
dc.contributor.author김범경-
dc.contributor.author한광협-
dc.contributor.author안상훈-
dc.date.accessioned2020-09-30T16:43:55Z-
dc.date.available2020-09-30T16:43:55Z-
dc.date.issued2020-07-
dc.identifier.issn0269-2813-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/179598-
dc.description.abstractBackground: Anti-viral therapy is not indicated for patients with chronic hepatitis B (CHB) in the immune-tolerant phase. Aims: To investigate the cumulative incidence of phase change and hepatocellular carcinoma (HCC) and independent predictors for phase change in patients with CHB in immune-tolerant phase. Methods: In total, 946 patients in immune-tolerant phase, defined as hepatitis B e antigen positivity, HBV-DNA >20 000 IU/mL and alanine aminotransferase (ALT) ≤40 IU/L, between 1989 and 2017 were enrolled from eight institutes. Results: The mean age of study population (429 men and 517 women) was 36.7 years. The mean ALT and HBV-DNA levels were 24.6 IU/L and 8.50 log10 IU/mL, respectively. Of the study population, 476 (50.3%) patients remained in immune-tolerant phase throughout the study period (median: 63.6 months). The cumulative incidence rates of phase change and HCC at 10 years were 70.7% and 1.7%, respectively. Multivariate analyses revealed that HBV-DNA level >107 IU/mL was associated independently with a reduced risk of phase change (hazard ratio [HR] = 0.734, P = 0.008), whereas a high ALT level, above the cut-off recommended in the Korean Association for the Study of the Liver guidelines (34 IU/L for men and 30 IU/L for women), was associated independently with a greater risk of phase change (HR = 1.885, P < 0.001). Conclusions: The criterion of HBV-DNA level > 107 IU/mL may be useful to define immune-tolerant phase. In addition, an extremely low risk of HCC development was observed in patients with CHB in immune-tolerant phase.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherWiley-Blackwell-
dc.relation.isPartOfALIMENTARY PHARMACOLOGY & THERAPEUTICS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleExtremely low risk of hepatocellular carcinoma development in patients with chronic hepatitis B in immune-tolerant phase-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorHan Ah Lee-
dc.contributor.googleauthorHyun Woong Lee-
dc.contributor.googleauthorIn Hee Kim-
dc.contributor.googleauthorSoo Young Park-
dc.contributor.googleauthorDong Hyun Sinn-
dc.contributor.googleauthorJung Hwan Yu-
dc.contributor.googleauthorYeon Seok Seo-
dc.contributor.googleauthorSoon Ho Um-
dc.contributor.googleauthorJung Il Lee-
dc.contributor.googleauthorKwan Sik Lee-
dc.contributor.googleauthorChang Hun Lee-
dc.contributor.googleauthorWon Young Tak-
dc.contributor.googleauthorYoung Oh Kweon-
dc.contributor.googleauthorWonseok Kang-
dc.contributor.googleauthorYong-Han Paik-
dc.contributor.googleauthorJin-Woo Lee-
dc.contributor.googleauthorSang Jun Suh-
dc.contributor.googleauthorYoung Kul Jung-
dc.contributor.googleauthorBeom Kyung Kim-
dc.contributor.googleauthorJun Yong Park-
dc.contributor.googleauthorDo Young Kim-
dc.contributor.googleauthorSang Hoon Ahn-
dc.contributor.googleauthorKwang-Hyub Han-
dc.contributor.googleauthorHyung Joon Yim-
dc.contributor.googleauthorSeung Up Kim-
dc.identifier.doi10.1111/apt.15741-
dc.contributor.localIdA01675-
dc.contributor.localIdA02666-
dc.contributor.localIdA03122-
dc.contributor.localIdA03292-
dc.contributor.localIdA00654-
dc.contributor.localIdA00385-
dc.contributor.localIdA00487-
dc.contributor.localIdA04268-
dc.contributor.localIdA02226-
dc.relation.journalcodeJ00061-
dc.identifier.eissn1365-2036-
dc.identifier.pmid32452564-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/full/10.1111/apt.15741-
dc.contributor.alternativeNamePark, Jun Yong-
dc.contributor.affiliatedAuthor박준용-
dc.contributor.affiliatedAuthor이관식-
dc.contributor.affiliatedAuthor이정일-
dc.contributor.affiliatedAuthor이현웅-
dc.contributor.affiliatedAuthor김승업-
dc.contributor.affiliatedAuthor김도영-
dc.contributor.affiliatedAuthor김범경-
dc.contributor.affiliatedAuthor한광협-
dc.contributor.affiliatedAuthor안상훈-
dc.citation.volume52-
dc.citation.number1-
dc.citation.startPage196-
dc.citation.endPage204-
dc.identifier.bibliographicCitationALIMENTARY PHARMACOLOGY & THERAPEUTICS, Vol.52(1) : 196-204, 2020-07-
dc.identifier.rimsid67335-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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