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

Authors :
Ömer Evirgen
Nail Ozgunes
Alper Gunduz
Mehmet Faruk Geyik
Serpil Erol
Hurrem Bodur
Neşe Demirtürk
Davut Ozdemir
Fatma Sargin
Ertugrul Guclu
Tuna Demirdal
Bahadir Ceylan
Ediz Tutuncu
Hasan Çetin Ekerbiçer
Kutbettin Demirdag
Nazan Tuna
Oguz Karabay
Saban Esen
Omer Faruk Kokoglu
Sıla Akhan
Mustafa Kasim Karahocagil
Selma Tosun
Guclu, E
Tuna, N
Karabay, O
Akhan, S
Bodur, H
Ceylan, B
Demirdal, T
Demirdag, K
Demirturk, N
Ekerbicer, H
Erol, S
Esen, S
Evirgen, O
Geyik, MF
Gunduz, A
Karahocagil, MK
Kokoglu, OF
Ozdemir, D
Ozgunes, N
Sargin, F
Tosun, S
Tutuncu, E
Sakarya Üniversitesi/Tıp Fakültesi/Dahili Tıp Bilimleri Bölümü
Güçlü, Ertuğrul
Karabay, Oğuz
Ekerbiçer, Hasan Çetin
Esen, Sinan
OMÜ
Publication Year :
2014

Abstract

Geyik, Mehmet Faruk/0000-0002-0906-0902; demirdal, tuna/0000-0002-9046-5666; KARABAY, OGUZ/0000-0003-1514-1685; Karabay, Oguz/0000-0003-0502-432X; Gunduz, Alper/0000-0001-9154-844X WOS: 000352106600012 PubMed: 25500658 Introduction: 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.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....7888e6c22ce24e730ea2d113473debd5