Predictors of response to pegylated interferon treatment in HBeAg-negative patients with chronic hepatitis B

dc.contributor.authorGuclu, Ertugrul
dc.contributor.authorTuna, Nazan
dc.contributor.authorKarabay, Oguz
dc.contributor.authorAkhan, Sila
dc.contributor.authorBodur, Hurrem
dc.contributor.authorCeylan, Bahadir
dc.contributor.authorTutuncu, Ediz
dc.date.accessioned2026-08-12T17:04:12Z
dc.date.issued2014
dc.departmentFırat Üniversitesi
dc.description.abstractIntroduction: Although pegylated interferons (pegIFNs) alpha-2a and alpha-2b have been used in chronic hepatitis B (CHB) treatment for many years, there are few studies concerning predictors of sustained virologic response (SVR) to pegIFN therapy. In this study, we aimed to investigate the predictors of response to pegIFN treatment in cases with HBeAg-negative CHB infection. Methodology: Seventeen tertiary care hospitals in Turkey were included in this study. Data from consecutively treated HBeAg-negative CHB patients, who received either pegIFN alpha-2a or alpha-2b, were collected retrospectively. SVR is defined as an HBV DNA concentration of less than 2,000 IU/mL six months after the completion of therapy Results: SVR was achieved in 40 (25%) of the 160 HBeAg-negative CHB patients. Viral loads in patients with SVR were lower compared to those with no SVR, beginning in the third month of treatment (p < 0.05). The number of cases with a decline of 1 log(10) IU/mL in viral load after the first month of treatment and with a serum HBV DNA level under 2,000 IU/mL after the third month of treatment was higher in cases with SVR (p < 0.05). The number of patients who had undetectable HBV DNA levels at week 48 among responders was significantly greater than among post-treatment virological relapsers (p < 0.05). Conclusions: Detection of a 1 log(10) decline in serum HBV DNA level at the first month of treatment and a serum HBV DNA level < 2000 IU/mL at the third month of therapy may be predictors of SVR.
dc.identifier.doi10.3855/jidc.4953
dc.identifier.endpage1608
dc.identifier.issn1972-2680
dc.identifier.issue12
dc.identifier.orcid0000-0002-9046-5666
dc.identifier.orcid0000-0002-5171-7306
dc.identifier.orcid0000-0002-6186-2494
dc.identifier.orcid0000-0003-1514-1685
dc.identifier.orcid0000-0001-9154-844X
dc.identifier.orcid0000-0002-7947-4692
dc.identifier.pmid25500658
dc.identifier.scopus2-s2.0-84918578225
dc.identifier.scopusqualityQ3
dc.identifier.startpage1601
dc.identifier.urihttps://doi.org/10.3855/jidc.4953
dc.identifier.urihttps://hdl.handle.net/11508/48630
dc.identifier.volume8
dc.identifier.wosWOS:000352106600012
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherJ Infection Developing Countries
dc.relation.ispartofJournal of Infection in Developing Countries
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjecthepatitis B
dc.subjectinterferon
dc.subjectsustained virological response
dc.subjectviral load
dc.titlePredictors of response to pegylated interferon treatment in HBeAg-negative patients with chronic hepatitis B
dc.typeArticle

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