1 662

Cited 127 times in

Prediction of development of liver-related events by transient elastography in Hepatitis B patients with complete virological response on antiviral therapy

DC Field Value Language
dc.contributor.author김승업-
dc.contributor.author박준용-
dc.contributor.author안상훈-
dc.contributor.author유은진-
dc.contributor.author이혜원-
dc.contributor.author한광협-
dc.contributor.author김도영-
dc.contributor.author김범경-
dc.date.accessioned2015-01-06T17:08:45Z-
dc.date.available2015-01-06T17:08:45Z-
dc.date.issued2014-
dc.identifier.issn0002-9270-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/99422-
dc.description.abstractOBJECTIVES: In the era of antiviral therapy, the prognostic significance of serum hepatitis B virus (HBV) DNA level as a biological gradient substantially diminished, as most patients can achieve complete virological response (CVR). We aimed to investigate the predictive roles of liver stiffness (LS) for liver-related events (LREs) among patients with CVR. METHODS: We analyzed 192 patients with chronic HBV infection who achieved CVR (defined as HBV DNA <20 IU/ml) through entecavir therapy. LS values at CVR were measured using transient elastography. LREs were defined as any cirrhotic complication, hepatocellular carcinoma, and liver-related mortality. RESULTS: The median age of the patients was 49 years, and 134 (69.8%) were male. The median LS value at CVR was 8.8 kPa. During follow-up, LREs occurred in 25 (13.0%) patients. When the population was stratified into three groups (<8.0 kPa, 8.0–13.0 kPa, and >13.0 kPa), cumulative LRE incidences increased significantly in association with LS values (log-rank test, P=0.001). Patients with an LS value >13.0 kPa (hazard ratio (HR)=12.336, 95% confidence interval (CI) 1.335–114.010; P=0.027) and 8.0–13.0 kPa (HR=8.832, 95% CI 1.092–71.432; P=0.041) were at significantly greater risk compared with those with an LS value <8.0 kPa. On multivariate analysis, age and LS values were seen to be independent predictors (all P<0.05). When LS values were incorporated into the REACH-B scoring model instead of serum HBV DNA level, a better predictive performance was seen compared with a conventional approach (areas under the receiver operating characteristic curve, 0.814 vs. 0.629, respectively). CONCLUSIONS: LS values at CVR are useful for predicting forthcoming LRE development. Thus, in the era of potent antiviral therapy, tailored surveillance strategies might be established based upon LS values at CVR.-
dc.description.statementOfResponsibilityopen-
dc.format.extent1241~1249-
dc.relation.isPartOfAMERICAN JOURNAL OF GASTROENTEROLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAntiviral Agents/therapeutic use*-
dc.subject.MESHBiomarkers, Tumor/blood-
dc.subject.MESHElasticity Imaging Techniques*-
dc.subject.MESHFemale-
dc.subject.MESHGuanine/analogs & derivatives*-
dc.subject.MESHGuanine/therapeutic use-
dc.subject.MESHHepatitis B, Chronic/diagnostic imaging*-
dc.subject.MESHHepatitis B, Chronic/drug therapy*-
dc.subject.MESHHumans-
dc.subject.MESHLiver Function Tests-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPredictive Value of Tests-
dc.subject.MESHProspective Studies-
dc.subject.MESHRepublic of Korea-
dc.titlePrediction of development of liver-related events by transient elastography in Hepatitis B patients with complete virological response on antiviral therapy-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorHye Won Lee-
dc.contributor.googleauthorEun Jin Yoo-
dc.contributor.googleauthorBeom Kyung Kim-
dc.contributor.googleauthorSeung Up Kim-
dc.contributor.googleauthorJun Yong Park-
dc.contributor.googleauthorDo Young Kim-
dc.contributor.googleauthorSang Hoon Ahn-
dc.contributor.googleauthorKwang-Hyub Han-
dc.identifier.doi10.1038/ajg.2014.157-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00654-
dc.contributor.localIdA01675-
dc.contributor.localIdA02226-
dc.contributor.localIdA02492-
dc.contributor.localIdA03318-
dc.contributor.localIdA04268-
dc.contributor.localIdA00487-
dc.contributor.localIdA00385-
dc.relation.journalcodeJ00081-
dc.identifier.eissn1572-0241-
dc.identifier.pmid24957159-
dc.identifier.urlhttp://www.nature.com/ajg/journal/v109/n8/full/ajg2014157a.html-
dc.contributor.alternativeNameKim, Seung Up-
dc.contributor.alternativeNamePark, Jun Yong-
dc.contributor.alternativeNameAhn, Sang Hoon-
dc.contributor.alternativeNameYoo, Eun Jin-
dc.contributor.alternativeNameLee, Hye Won-
dc.contributor.alternativeNameHan, Kwang Hyup-
dc.contributor.alternativeNameKim, Do Young-
dc.contributor.alternativeNameKim, Beom Kyung-
dc.contributor.affiliatedAuthorKim, Seung Up-
dc.contributor.affiliatedAuthorPark, Jun Yong-
dc.contributor.affiliatedAuthorAhn, Sang Hoon-
dc.contributor.affiliatedAuthorYoo, Eun Jin-
dc.contributor.affiliatedAuthorLee, Hye Won-
dc.contributor.affiliatedAuthorHan, Kwang Hyup-
dc.contributor.affiliatedAuthorKim, Beom Kyung-
dc.contributor.affiliatedAuthorKim, Do Young-
dc.rights.accessRightsfree-
dc.citation.volume109-
dc.citation.number8-
dc.citation.startPage1241-
dc.citation.endPage1249-
dc.identifier.bibliographicCitationAMERICAN JOURNAL OF GASTROENTEROLOGY, Vol.109(8) : 1241-1249, 2014-
dc.identifier.rimsid39417-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.