Association between level of hepatitis d virus RNA at week 24 of pegylated interferon therapy and outcome
dc.contributor.author | Keskin, Onur | |
dc.contributor.author | Wedemeyer, Heiner | |
dc.contributor.author | Tüzün, Ali | |
dc.contributor.author | Zachou, Kalliopi | |
dc.contributor.author | Deda, Xheni | |
dc.contributor.author | Dalekos, George N. | |
dc.contributor.author | Heidrich, Benjamin | |
dc.contributor.author | Pehlivan, Selcen | |
dc.contributor.author | Zeuzem, Stefan | |
dc.contributor.author | Yalçın, Kendal | |
dc.contributor.author | Tabak, Fehmi | |
dc.contributor.author | İdilman, Ramazan | |
dc.contributor.author | Bozkaya, Hakan | |
dc.contributor.author | Manns, Michael | |
dc.contributor.author | Yurdaydın, Cihan | |
dc.contributor.buuauthor | Gürel, Selim | |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Gastroenteroloji Anabilim Dalı. | tr_TR |
dc.contributor.scopusid | 7003706434 | tr_TR |
dc.date.accessioned | 2022-06-13T07:27:17Z | |
dc.date.available | 2022-06-13T07:27:17Z | |
dc.date.issued | 2015-12 | |
dc.description.abstract | BACKGROUND & 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. | en_US |
dc.description.sponsorship | Hep-Net Germany (German Ministry for Education and Research, BMBF-Forderkennzeichen) | en_US |
dc.description.sponsorship | Roche Turkey | en_US |
dc.identifier.citation | Keskin, 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. | en_US |
dc.identifier.endpage | 2349 | tr_TR |
dc.identifier.issn | 1542-3565 | |
dc.identifier.issue | 13 | tr_TR |
dc.identifier.pubmed | 26044319 | tr_TR |
dc.identifier.scopus | 2-s2.0-84947244327 | tr_TR |
dc.identifier.startpage | 2342 | tr_TR |
dc.identifier.uri | https://doi.org/10.1016/j.cgh.2015.05.029 | |
dc.identifier.uri | https://www.sciencedirect.com/science/article/abs/pii/S1542356515007648 | |
dc.identifier.uri | http://hdl.handle.net/11452/27085 | |
dc.identifier.volume | 13 | tr_TR |
dc.identifier.wos | 000365191300025 | |
dc.indexed.pubmed | PubMed | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.wos | SCIE | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.relation.collaboration | Yurt dışı | tr_TR |
dc.relation.collaboration | Sanayi | tr_TR |
dc.relation.journal | Clinical Gastroenterology and Hepatology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Chronic delta hepatitis | en_US |
dc.subject | On-treatment HDV RNA | en_US |
dc.subject | Pegylated interferon treatment | en_US |
dc.subject | Treatment outcome prediction | en_US |
dc.subject | Chronic delta-hepatitis | en_US |
dc.subject | Peginterferon alpha-2a | en_US |
dc.subject | Kinetics | en_US |
dc.subject | Interleukin-28b | en_US |
dc.subject | Polymorphisms | en_US |
dc.subject | Ribavirin | en_US |
dc.subject | Efficacy | en_US |
dc.subject | Hbsag | en_US |
dc.subject | Drug | en_US |
dc.subject | Gastroenterology & hepatology | en_US |
dc.subject.emtree | Adefovir | en_US |
dc.subject.emtree | Adefovir dipivoxil | en_US |
dc.subject.emtree | Hepatitis B surface antigen | en_US |
dc.subject.emtree | Liver enzyme | en_US |
dc.subject.emtree | Peginterferon alpha2a | en_US |
dc.subject.emtree | Placebo | en_US |
dc.subject.emtree | Virus DNA | en_US |
dc.subject.emtree | Virus RNA | en_US |
dc.subject.emtree | Adenine | en_US |
dc.subject.emtree | Alpha interferon | en_US |
dc.subject.emtree | Aminotransferase | en_US |
dc.subject.emtree | Antivirus agent | en_US |
dc.subject.emtree | Hepatitis B surface antigen | en_US |
dc.subject.emtree | Macrogol derivative | en_US |
dc.subject.emtree | Peginterferon alpha2a | en_US |
dc.subject.emtree | Phosphonic acid derivative | en_US |
dc.subject.emtree | Placebo | en_US |
dc.subject.emtree | Recombinant protein | en_US |
dc.subject.emtree | Virus DNA | en_US |
dc.subject.emtree | Virus RNA | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Clinical article | en_US |
dc.subject.emtree | Combination chemotherapy | en_US |
dc.subject.emtree | Controlled clinical trial | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Delta agent hepatitis | en_US |
dc.subject.emtree | Disease association | en_US |
dc.subject.emtree | Drug efficacy | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Follow up | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Human tissue | en_US |
dc.subject.emtree | Liver biopsy | en_US |
dc.subject.emtree | Liver fibrosis | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Monotherapy | en_US |
dc.subject.emtree | Nonhuman | en_US |
dc.subject.emtree | Outcome assessment | en_US |
dc.subject.emtree | Predictive value | en_US |
dc.subject.emtree | Treatment duration | en_US |
dc.subject.emtree | Treatment response | en_US |
dc.subject.emtree | Analogs and derivatives | en_US |
dc.subject.emtree | Biopsy | en_US |
dc.subject.emtree | Blood | en_US |
dc.subject.emtree | Clinical trial | en_US |
dc.subject.emtree | Genetics | en_US |
dc.subject.emtree | Hepatitis D, Chronic | en_US |
dc.subject.emtree | Hepatitis delta virus | en_US |
dc.subject.emtree | Isolation and purification | en_US |
dc.subject.emtree | Liver cirrhosis | en_US |
dc.subject.emtree | Middle aged | en_US |
dc.subject.emtree | Pathology | en_US |
dc.subject.emtree | Treatment outcome | en_US |
dc.subject.emtree | Virus load | en_US |
dc.subject.mesh | Adenine | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Antiviral agents | en_US |
dc.subject.mesh | Biopsy | en_US |
dc.subject.mesh | DNA, viral | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Hepatitis B surface antigens | en_US |
dc.subject.mesh | Hepatitis D, chronic | en_US |
dc.subject.mesh | Hepatitis delta virus | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Interferon-alpha | en_US |
dc.subject.mesh | Liver cirrhosis | tr_TR |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle aged | en_US |
dc.subject.mesh | Organophosphonates | en_US |
dc.subject.mesh | Placebos | en_US |
dc.subject.mesh | Polyethylene glycols | en_US |
dc.subject.mesh | Recombinant proteins | en_US |
dc.subject.mesh | RNA, viral | en_US |
dc.subject.mesh | Transaminases | en_US |
dc.subject.mesh | Treatment outcome | en_US |
dc.subject.mesh | Viral load | en_US |
dc.subject.scopus | Hepatitis Delta Virus; Chronic Hepatitis D; Hepatitis B | en_US |
dc.subject.wos | Gastroenterology & hepatology | en_US |
dc.title | Association between level of hepatitis d virus RNA at week 24 of pegylated interferon therapy and outcome | en_US |
dc.type | Article | |
dc.wos.quartile | Q1 | en_US |
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