Publication:
Association between level of hepatitis d virus RNA at week 24 of pegylated interferon therapy and outcome

dc.contributor.authorKeskin, Onur
dc.contributor.authorWedemeyer, Heiner
dc.contributor.authorTüzün, Ali
dc.contributor.authorZachou, Kalliopi
dc.contributor.authorDeda, Xheni
dc.contributor.authorDalekos, George N.
dc.contributor.authorHeidrich, Benjamin
dc.contributor.authorPehlivan, Selcen
dc.contributor.authorZeuzem, Stefan
dc.contributor.authorYalçın, Kendal
dc.contributor.authorTabak, Fehmi
dc.contributor.authorİdilman, Ramazan
dc.contributor.authorBozkaya, Hakan
dc.contributor.authorManns, Michael
dc.contributor.authorYurdaydın, Cihan
dc.contributor.buuauthorGürel, Selim
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentGastroenteroloji Ana Bilim Dalı
dc.contributor.scopusid7003706434
dc.date.accessioned2022-06-13T07:27:17Z
dc.date.available2022-06-13T07:27:17Z
dc.date.issued2015-12
dc.description.abstractBACKGROUND & AIMS: Interferon is the only effective treatment for chronic hepatitis D virus (HDV) infection. No rules have been set for stopping treatment based on viral kinetics. We analyzed data from an international study of hepatitis D treatment to identify factors associated with outcomes of pegylated interferon treatment, with and without adefovir. METHODS: We analyzed data from the Hep-Net-International Delta Hepatitis Intervention Trial on 50 patients with compensated liver disease who tested positive for anti-HDV and HDV RNA. Subjects received pegylated interferon alpha 2a, with adefovir or placebo, or only adefovir, for 48 weeks. Twenty-four weeks after treatment ended, 41 patients were evaluated for levels of HDV RNA and DNA, liver enzymes, and hepatitis B surface antigen (HBsAg); liver biopsy specimens were analyzed for fibrosis. Response to therapy was defined as end-of-treatment response or post-treatment week 24 virologic response. In both cases virologic response was associated with undetectable HDV RNA levels. Patients with less than a 1 log decrease in HDV RNA at the end of treatment were considered null responders. RESULTS: Based on univariate and multivariate analysis, the level of HDV RNA at week 24 of treatment was associated more strongly with response to therapy than other factors analyzed. The level of HBsAg at week 24 of treatment was associated with a response to therapy only in univariate analysis. Lack of HDV RNA at week 24 of treatment, or end of treatment, identified responders with positive predicted values of 71% and 100%, respectively. At 24 weeks after treatment, a decrease in HDV RNA level of less than 1 log, combined with no decrease in HBsAg level, identified null responders with a positive predictive value of 83%. A decrease in HDV RNA level of more than 2 log at week 24 of treatment identified null responders with a negative predictive value of 95%. CONCLUSIONS: Based on an analysis of data from a large clinical trial, the level of HDV RNA at week 24 of treatment with pegylated interferon, with or without adefovir for 48 weeks, can identify patients who will test negative for HDV RNA 24 weeks after the end of treatment. This information can be used to help physicians manage patients receiving therapy for chronic hepatitis D.
dc.description.sponsorshipHep-Net Germany (German Ministry for Education and Research, BMBF-Forderkennzeichen)
dc.description.sponsorshipRoche Turkey
dc.identifier.citationKeskin, O. vd. (2015). "Association between level of hepatitis d virus RNA at week 24 of pegylated interferon therapy and outcome". Clinical Gastroenterology and Hepatology, 13(13), 2342-2349.
dc.identifier.endpage2349
dc.identifier.issn1542-3565
dc.identifier.issue13
dc.identifier.pubmed26044319
dc.identifier.scopus2-s2.0-84947244327
dc.identifier.startpage2342
dc.identifier.urihttps://doi.org/10.1016/j.cgh.2015.05.029
dc.identifier.urihttps://www.sciencedirect.com/science/article/abs/pii/S1542356515007648
dc.identifier.urihttp://hdl.handle.net/11452/27085
dc.identifier.volume13
dc.identifier.wos000365191300025
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherElsevier
dc.relation.collaborationYurt içi
dc.relation.collaborationYurt dışı
dc.relation.collaborationSanayi
dc.relation.journalClinical Gastroenterology and Hepatology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectChronic delta hepatitis
dc.subjectOn-treatment HDV RNA
dc.subjectPegylated interferon treatment
dc.subjectTreatment outcome prediction
dc.subjectChronic delta-hepatitis
dc.subjectPeginterferon alpha-2a
dc.subjectKinetics
dc.subjectInterleukin-28b
dc.subjectPolymorphisms
dc.subjectRibavirin
dc.subjectEfficacy
dc.subjectHbsag
dc.subjectDrug
dc.subjectGastroenterology & hepatology
dc.subject.emtreeAdefovir
dc.subject.emtreeAdefovir dipivoxil
dc.subject.emtreeHepatitis B surface antigen
dc.subject.emtreeLiver enzyme
dc.subject.emtreePeginterferon alpha2a
dc.subject.emtreePlacebo
dc.subject.emtreeVirus DNA
dc.subject.emtreeVirus RNA
dc.subject.emtreeAdenine
dc.subject.emtreeAlpha interferon
dc.subject.emtreeAminotransferase
dc.subject.emtreeAntivirus agent
dc.subject.emtreeHepatitis B surface antigen
dc.subject.emtreeMacrogol derivative
dc.subject.emtreePeginterferon alpha2a
dc.subject.emtreePhosphonic acid derivative
dc.subject.emtreePlacebo
dc.subject.emtreeRecombinant protein
dc.subject.emtreeVirus DNA
dc.subject.emtreeVirus RNA
dc.subject.emtreeAdult
dc.subject.emtreeArticle
dc.subject.emtreeClinical article
dc.subject.emtreeCombination chemotherapy
dc.subject.emtreeControlled clinical trial
dc.subject.emtreeControlled study
dc.subject.emtreeDelta agent hepatitis
dc.subject.emtreeDisease association
dc.subject.emtreeDrug efficacy
dc.subject.emtreeFemale
dc.subject.emtreeFollow up
dc.subject.emtreeHuman
dc.subject.emtreeHuman tissue
dc.subject.emtreeLiver biopsy
dc.subject.emtreeLiver fibrosis
dc.subject.emtreeMale
dc.subject.emtreeMonotherapy
dc.subject.emtreeNonhuman
dc.subject.emtreeOutcome assessment
dc.subject.emtreePredictive value
dc.subject.emtreeTreatment duration
dc.subject.emtreeTreatment response
dc.subject.emtreeAnalogs and derivatives
dc.subject.emtreeBiopsy
dc.subject.emtreeBlood
dc.subject.emtreeClinical trial
dc.subject.emtreeGenetics
dc.subject.emtreeHepatitis D, Chronic
dc.subject.emtreeHepatitis delta virus
dc.subject.emtreeIsolation and purification
dc.subject.emtreeLiver cirrhosis
dc.subject.emtreeMiddle aged
dc.subject.emtreePathology
dc.subject.emtreeTreatment outcome
dc.subject.emtreeVirus load
dc.subject.meshAdenine
dc.subject.meshAdult
dc.subject.meshAntiviral agents
dc.subject.meshBiopsy
dc.subject.meshDNA, viral
dc.subject.meshFemale
dc.subject.meshHepatitis B surface antigens
dc.subject.meshHepatitis D, chronic
dc.subject.meshHepatitis delta virus
dc.subject.meshHumans
dc.subject.meshInterferon-alpha
dc.subject.meshLiver cirrhosis
dc.subject.meshMale
dc.subject.meshMiddle aged
dc.subject.meshOrganophosphonates
dc.subject.meshPlacebos
dc.subject.meshPolyethylene glycols
dc.subject.meshRecombinant proteins
dc.subject.meshRNA, viral
dc.subject.meshTransaminases
dc.subject.meshTreatment outcome
dc.subject.meshViral load
dc.subject.scopusHepatitis Delta Virus; Chronic Hepatitis D; Hepatitis B
dc.subject.wosGastroenterology & hepatology
dc.titleAssociation between level of hepatitis d virus RNA at week 24 of pegylated interferon therapy and outcome
dc.typeArticle
dc.wos.quartileQ1
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Gastroenteroloji Ana Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

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