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Association between polymorphism of tumor necrosis factor-alpha promoter and response to lamivudine treatment in patients with chronic hepatitis B.

DC Field Value Language
dc.contributor.author박용광-
dc.contributor.author박준용-
dc.contributor.author안상훈-
dc.contributor.author이관식-
dc.contributor.author이중민-
dc.contributor.author장혜영-
dc.contributor.author한광협-
dc.contributor.author김도영-
dc.contributor.author김자경-
dc.date.accessioned2015-04-23T17:06:57Z-
dc.date.available2015-04-23T17:06:57Z-
dc.date.issued2010-
dc.identifier.issn0163-2116-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/101849-
dc.description.abstractBACKGROUND: TNF-alpha promoter polymorphism is known to play an important role in the immunopathogenesis of infection of hepatitis B virus. AIMS: We investigated whether polymorphisms of TNF-alpha promoter at position -308 or -238 had associations with the response to lamivudine treatment. METHODS: A total of 89 healthy subjects (control group) and 225 patients with chronic hepatitis B treated with lamivudine were included in this study. Polymorphisms of TNF-alpha promoter at position -308 and -238 were analyzed by polymerase chain reaction. Recruited patients were classified according to the outcome of lamivudine treatment into the responder (103 patients) or non-responder (122 patients) group. RESULTS: The numbers of A allelic polymorphism of TNF-alpha promoter at position -238 were four (2.2%) in the control, five (2.4%) in the responder and 19 (7.8%) in the non-responder group. The A allele was noted significantly more frequently in the responder than non-responder group (P = 0.012). At position -308, a significant difference was observed between the control group (14; 7.9%) and total chronic hepatitis B patients (15; 3.3%) (P = 0.015). CONCLUSIONS: Our study demonstrated that the non-response to lamivudine treatment in patients with chronic hepatitis B might be related to the A allelic polymorphism of TNF-alpha promoter at position -238.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfDIGESTIVE DISEASES AND SCIENCES-
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.MESHAnalysis of Variance-
dc.subject.MESHCase-Control Studies-
dc.subject.MESHConfidence Intervals-
dc.subject.MESHDisease Progression-
dc.subject.MESHFemale-
dc.subject.MESHFollow-Up Studies-
dc.subject.MESHGene Expression Regulation-
dc.subject.MESHGenotype-
dc.subject.MESHHepatitis B, Chronic/diagnosis-
dc.subject.MESHHepatitis B, Chronic/drug therapy*-
dc.subject.MESHHepatitis B, Chronic/genetics*-
dc.subject.MESHHumans-
dc.subject.MESHLamivudine/therapeutic use*-
dc.subject.MESHLiver Function Tests-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMultivariate Analysis-
dc.subject.MESHOdds Ratio-
dc.subject.MESHPolymorphism, Genetic*-
dc.subject.MESHProbability-
dc.subject.MESHPromoter Regions, Genetic/drug effects*-
dc.subject.MESHReference Values-
dc.subject.MESHRisk Assessment-
dc.subject.MESHSeverity of Illness Index-
dc.subject.MESHTreatment Failure-
dc.subject.MESHTreatment Outcome-
dc.subject.MESHTumor Necrosis Factor-alpha/genetics*-
dc.subject.MESHTumor Necrosis Factor-alpha/metabolism-
dc.subject.MESHYoung Adult-
dc.titleAssociation between polymorphism of tumor necrosis factor-alpha promoter and response to lamivudine treatment in patients with chronic hepatitis B.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorYong Kwang Park-
dc.contributor.googleauthorJung Min Lee-
dc.contributor.googleauthorDo Young Kim-
dc.contributor.googleauthorHye Young Chang-
dc.contributor.googleauthorJa Kyung Kim-
dc.contributor.googleauthorChun Kyon Lee-
dc.contributor.googleauthorJun Yong Park-
dc.contributor.googleauthorSang Hoon Ahn-
dc.contributor.googleauthorKwan Sik Lee-
dc.contributor.googleauthorKwang Hyub Han-
dc.identifier.doi10.1007/s10620-009-0983-1-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01577-
dc.contributor.localIdA01675-
dc.contributor.localIdA02226-
dc.contributor.localIdA02666-
dc.contributor.localIdA03252-
dc.contributor.localIdA03495-
dc.contributor.localIdA04268-
dc.contributor.localIdA00852-
dc.contributor.localIdA03184-
dc.contributor.localIdA00385-
dc.relation.journalcodeJ00737-
dc.identifier.eissn1573-2568-
dc.identifier.pmid19830555-
dc.identifier.urlhttp://link.springer.com/article/10.1007%2Fs10620-009-0983-1-
dc.subject.keywordHepatitis B virus-
dc.subject.keywordLamivudine-
dc.subject.keywordTumor necrosis factor-alpha-
dc.subject.keywordSingle nucleotide polymorphism-
dc.contributor.alternativeNamePark, Yong Kwang-
dc.contributor.alternativeNamePark, Jun Yong-
dc.contributor.alternativeNameAhn, Sang Hoon-
dc.contributor.alternativeNameLee, Kwan Sik-
dc.contributor.alternativeNameLee, Jung Min-
dc.contributor.alternativeNameLee, Chun Kyon-
dc.contributor.alternativeNameChang, Hye Young-
dc.contributor.alternativeNameHan, Kwang Hyup-
dc.contributor.alternativeNameKim, Do Young-
dc.contributor.alternativeNameKim, Ja Kyung-
dc.contributor.affiliatedAuthorPark, Yong Kwang-
dc.contributor.affiliatedAuthorPark, Jun Yong-
dc.contributor.affiliatedAuthorAhn, Sang Hoon-
dc.contributor.affiliatedAuthorLee, Kwan Sik-
dc.contributor.affiliatedAuthorLee, Chun Kyon-
dc.contributor.affiliatedAuthorChang, Hye Young-
dc.contributor.affiliatedAuthorHan, Kwang Hyup-
dc.contributor.affiliatedAuthorKim, Ja Kyung-
dc.contributor.affiliatedAuthorLee, Jung Min-
dc.contributor.affiliatedAuthorKim, Do Young-
dc.citation.volume55-
dc.citation.number7-
dc.citation.startPage2043-
dc.citation.endPage2048-
dc.identifier.bibliographicCitationDIGESTIVE DISEASES AND SCIENCES, Vol.55(7) : 2043-2048, 2010-
dc.identifier.rimsid54651-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers

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