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dc.contributor.authorKarabay, Oguz
dc.contributor.authorTuna, Nazan
dc.contributor.authorEsen, Saban
dc.date.accessioned2020-06-21T14:17:29Z
dc.date.available2020-06-21T14:17:29Z
dc.date.issued2012
dc.identifier.issn0954-691X
dc.identifier.issn1473-5687
dc.identifier.urihttps://doi.org/10.1097/MEG.0b013e328356eac2
dc.identifier.urihttps://hdl.handle.net/20.500.12712/16285
dc.descriptionKARABAY, OGUZ/0000-0003-1514-1685; Karabay, Oguz/0000-0003-0502-432Xen_US
dc.descriptionWOS: 000309553900009en_US
dc.descriptionPubMed: 22825647en_US
dc.description.abstractIntroduction Interferons, pegylated interferons (PegIFN), and oral antivirals are used in the treatment of chronic hepatitis B (CHB) virus infection. The number of studies comparing the efficacy of PegIFNs in the treatment of HBe antigen-negative CHB is rather limited. In this trial, the efficacy of two PegIFN products used in the treatment of CHB is compared. Methods Study data were obtained from 16 tertiary healthcare service centers located in various areas of Turkey. Data of patients who were consecutively treated with PegIFN alpha-2a or alpha-2b for CHB were recorded retrospectively. Hepatitis B virus DNA and liver enzymes were analyzed at the beginning of the treatment and during weeks 12, 24, 48, and 72. A P-value less than 0.05 was considered to be significant. Results A total of 155 patients were enrolled in this trial. Two cases were excluded because of insufficient data. Among the remaining 153 patients, 81 (53%) patients were in the PegIFN alpha-2a group and 72 (47%) patients were in the alpha-2b group. Treatment success was found to be 17.2% for the PegIFN alpha-2a group and 18.0% for the PegIFN alpha-2b group (P>0.05). In terms of efficacy (weeks 24, 48, and 72), there were no significant differences between the groups (P>0.05). Conclusion According to our results, for HBe antigen-negative CHB cases, the response rate during the sixth month after the treatment with PegIFN was determined to be similar to 17%. No difference was found between the efficacy rates of the two PegIFN products used in the treatment of HBe antigen-negative CHB. Eur J Gastroenterol Hepatol 24: 1296-1301 (C) 2012 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.en_US
dc.description.sponsorshipHEP-NET Turkey; Gliad scienceen_US
dc.description.sponsorshipThe authors thank the HEP-NET Turkey project for support. Planning the study: K. Oguz. Conducting the study: K. Oguz, T. Nazan. Collecting data: K. Oguz, T. Nazan, E. Saban and the PEG-HBV study group (arranged in alphabetical order: A. Sila, B. Hurrem, C. Bahadir, D. Kutbettin, D. Tuna, D. Nese, E. Serpil, E. Omer, G. Faruk, G. Alper, K.K. Mustafa, F.K. Omer, O. Resat, O. Davut, O. Nail, S. Fatma, T. Ediz). Interpreting data: K. Oguz and T. Nazan. Drafting the manuscript: K. Oguz, T. Nazan, E. Saban.; K. Oguz and T. Nazan received travel and manuscript preparation (statistical analysis) grants from Gliad science. For the remaining authors there are no conflicts of interest.en_US
dc.language.isoengen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.isversionof10.1097/MEG.0b013e328356eac2en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectchronic hepatitis Ben_US
dc.subjectpegylated interferonen_US
dc.subjecttreatmenten_US
dc.titleComparative efficacy of pegylated interferons alpha-2a and 2b in the treatment of HBeAg-negative chronic Hepatitis B infectionen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume24en_US
dc.identifier.issue11en_US
dc.identifier.startpage1296en_US
dc.identifier.endpage1301en_US
dc.relation.journalEuropean Journal of Gastroenterology & Hepatologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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