## Abstract For chronic hepatitis C virus (HCV) infection, evaluation of response to peginterferon (PEGβIFN) plus ribavirin (RBV) therapy based on viral kinetics is useful as an early predictor of treatment efficacy, but the underlying mechanisms of the different viral kinetics to treatment are sti
Prediction of response to peginterferon-alfa-2b plus ribavirin therapy in Japanese patients infected with hepatitis C virus genotype 1b
β Scribed by Yoshimasa Hashimoto; Hidenori Ochi; Hiromi Abe; Yasufumi Hayashida; Masataka Tsuge; Fukiko Mitsui; Nobuhiko Hiraga; Michio Imamura; Shoichi Takahashi; C. Nelson Hayes; Waka Ohishi; Michaki Kubo; Tatsuhiko Tsunoda; Naoyuki Kamatani; Yusuke Nakamura; Kazuaki Chayama
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 174 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0146-6615
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β¦ Synopsis
Abstract
Variation at the ILβ28B locus was recently reported to be a significant predictive factor of viral response to pegylatedβinterferon plus ribavirin combination therapy against chronic hepatitis C. Predictive factors for the effect of therapy, including ILβ28B polymorphism rs8099917 and viral and clinical factors were investigated. A total of 288 patients were enrolled who were chronically infected with hepatitis C virus (HCV) genotype 1b and treated with combination therapy. Among them, 87 patients completed 48 weeks of therapy without dose reduction or discontinuation. In multivariate regression analysis, the rs8099917 TT genotype was the only independent factor significantly associated with sustained viral response (Pβ=β0.016, OR 61.5), whereas substitutions at amino acid 70 (aa 70) of the HCV core protein (Pβ=β0.038, OR 5.9) and nonβTT genotypes (Pβ=β0.002, OR 17.2) were associated with nonvirological response. Both factors were also associated with viral dynamics during the initial stage of the therapy. Correlation analysis revealed that rs8099917 genotype was correlated with Ξ³βglutamyl transpeptidase, hyaluronic acid, and HCV core aa 70. In conclusion, host (ILβ28B polymorphism) and viral (aa 70) factors independently affect response to combination therapy. J. Med. Virol. 83:981β988, 2011. Β© 2011 WileyβLiss, Inc.
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