Literature DB >> 7506584

Factors useful in predicting the response to interferon therapy in chronic hepatitis C.

A Tsubota1, K Chayama, Y Arase, I Koida, S Saitoh, K Ikeda, S Iwasaki, T Matsumoto, M Kobayashi, H Kumada.   

Abstract

To determine how various factors influence the response to interferon (IFN) therapy, we retrospectively studied 157 consecutive Japanese patients with chronic hepatitis C who received various treatment schedules of IFN. They were divided into two groups on the bases of outcome. One group was comprised of 65 patients who achieved a sustained normalization of serum alanine aminotransferase (ALT) levels for at least 6 months after treatment, while the other group was comprised of 84 patients with persistent elevation of serum ALT levels, despite treatment. Genotyping of hepatitis C virus (HCV) was done by polymerase chain reaction (PCR) with genotype specific primers, analysing the variations in nucleotide sequence within the NS 5 region of the HCV genome, namely genotypes PT, K1, K2a and K2b. We then used a multivariate analysis to determine the factors related to mode of treatment, patient characteristics and HCV genotype in relation to the response to IFN therapy. Of the 16 factors analysed, the HCV genotype (genotype K2a or K2b, P < 0.0008), treatment schedule (intermittent administration following a daily schedule, designated as combined schedule, P > 0.0014) and liver histology just before treatment (chronic persistent hepatitis or mild chronic aggressive hepatitis, P < 0.0324) were the most strongly correlated with a normalizing response to IFN therapy. These results suggest that not only are the IFN treatment schedule and patient profile significant, but the properties of the virus also influences the response. However, as the IFN treatment schedule is the only changeable factor, it should be designed to maximize the benefit of IFN therapy.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 7506584     DOI: 10.1111/j.1440-1746.1993.tb01648.x

Source DB:  PubMed          Journal:  J Gastroenterol Hepatol        ISSN: 0815-9319            Impact factor:   4.029


  14 in total

1.  Recent advances in laboratory diagnosis of hepatitis C virus infection.

Authors:  R Chaudhary
Journal:  Can J Infect Dis       Date:  1994-11

2.  Subtyping of hepatitis C virus isolates by a line probe assay using hybridization.

Authors:  A Andonov; R K Chaudhary
Journal:  J Clin Microbiol       Date:  1995-01       Impact factor: 5.948

3.  Predictors of response to interferon therapy.

Authors:  G Saracco; M Rizzetto
Journal:  Dig Dis Sci       Date:  1996-12       Impact factor: 3.199

4.  Pharmacokinetics of ribavirin in combined interferon-alpha 2b and ribavirin therapy for chronic hepatitis C virus infection.

Authors:  Akihito Tsubota; Yuichi Hirose; Namiki Izumi; Hiromitsu Kumada
Journal:  Br J Clin Pharmacol       Date:  2003-04       Impact factor: 4.335

5.  Interferon-λ3 polymorphisms in pegylated-interferon-α plus ribavirin therapy for genotype-2 chronic hepatitis C.

Authors:  Haruya Ishiguro; Hiroshi Abe; Nobuyoshi Seki; Tomonori Sugita; Yuta Aida; Munenori Itagaki; Satoshi Sutoh; Noritomo Shimada; Tomomi Furihata; Akihito Tsubota; Yoshio Aizawa
Journal:  World J Gastroenterol       Date:  2015-04-07       Impact factor: 5.742

6.  Relationship between pretreatment viremia level and response to interferon-alpha therapy in chronic hepatitis C differs in viral type 1 and 2 infections.

Authors:  A Tsubota; H Kumada; K Chayama; Y Arase; S Saitoh; I Koida; N Murashima; Y Suzuki; M Kobayashi; K Takagi; M Kobayashi; K Ikeda
Journal:  Dig Dis Sci       Date:  1996-10       Impact factor: 3.199

7.  Interferon treatment of chronic hepatitis C in patients with hemophilia or von Willebrand's disease in Japan.

Authors:  M Yoshikawa; H Fukui; H Kojima; H Yoshiji; T Sakamoto; H Imazu; T Nakanani; Y Matsumura; S Kuriyama; J Yamao
Journal:  J Gastroenterol       Date:  1995-06       Impact factor: 7.527

8.  Genotypes and virus load in patients with hepatitis C infection.

Authors:  H Hofmann
Journal:  Infection       Date:  1995 May-Jun       Impact factor: 3.553

9.  Replicative homeostasis III: implications for antiviral therapy and mechanisms of response and non-response.

Authors:  Richard Sallie
Journal:  Virol J       Date:  2007-03-13       Impact factor: 4.099

10.  Evolution of hepatitis C virus quasispecies in hypervariable region 1 and the putative interferon sensitivity-determining region during interferon therapy and natural infection.

Authors:  S J Polyak; S McArdle; S L Liu; D G Sullivan; M Chung; W T Hofgärtner; R L Carithers; B J McMahon; J I Mullins; L Corey; D R Gretch
Journal:  J Virol       Date:  1998-05       Impact factor: 5.103

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.