Literature DB >> 17627640

Management of HBV infection in Japan.

Masahito Minami1, Takeshi Okanoue.   

Abstract

Hepatitis B virus (HBV) is usually transmitted from mother to infant, and genotype C is prevalent in Japan. Because of these features, guidelines for HBV treatment from other countries are not directly adaptable to Japanese patients. Age is an important factor in deciding the treatment strategy, because many vertically transmitted HBV carriers naturally show spontaneous remission by the age of 25-30 years. In addition, genotype C is considered more refractory to antiviral therapies than genotypes A and B. Considering these differences, we propose a treatment for HBV in Japanese patients. Although the guidelines indicate who to treat and when therapy should be started, it is unclear for how long patientsshould be treated. This situation arises because current lamivudine and interferon monotherapies are not potent at curing HBV infection. To develop a more efficient treatment, we performed a pilot study of lamivudine/interferon sequential therapy in Japan. The biochemical and virological responses were comparable or superior to lamivudine or interferon monotherapies, and this protocol can be a potent alternative because we can take advantage of both the mild side-effects of lamivudine and finite duration of interferon.

Entities:  

Year:  2007        PMID: 17627640     DOI: 10.1111/j.1872-034X.2007.00109.x

Source DB:  PubMed          Journal:  Hepatol Res        ISSN: 1386-6346            Impact factor:   4.288


  6 in total

1.  Combinational use of hepatitis B viral antigens predicts responses to nucleos(t)ide analogue/peg-interferon sequential therapy.

Authors:  Akihiro Matsumoto; Shuhei Nishiguchi; Hirayuki Enomoto; Jong-Hon Kang; Yasuhito Tanaka; Noboru Shinkai; Masayuki Kurosaki; Masaru Enomoto; Tatsuo Kanda; Osamu Yokosuka; Hiroshi Yatsuhashi; Shinya Nagaoka; Chiaki Okuse; Tatehiro Kagawa; Tetsuya Mine; Koichi Takaguchi; Satoru Saito; Keisuke Hino; Fusao Ikeda; Shotaro Sakisaka; Daisuke Morihara; Shiho Miyase; Masataka Tsuge; Kazuaki Chayama; Naoki Hiramatsu; Yoshiyuki Suzuki; Kazumoto Murata; Eiji Tanaka
Journal:  J Gastroenterol       Date:  2017-06-20       Impact factor: 7.527

2.  Interferon and nucleoside analog combination therapy for hepatitis B.

Authors:  Masahito Minami; Takayuki Katayama; Rei Sendo; Takeshi Okanoue; Toshikazu Yoshikawa
Journal:  Clin J Gastroenterol       Date:  2010-02-23

Review 3.  Combination therapy with a nucleos(t)ide analogue and interferon for chronic hepatitis B: simultaneous or sequential.

Authors:  Masaru Enomoto; Akihiro Tamori; Shuhei Nishiguchi; Norifumi Kawada
Journal:  J Gastroenterol       Date:  2013-01-22       Impact factor: 7.527

4.  Current treatment for chronic hepatitis B in Japan.

Authors:  Waka Ohishi; Kazuaki Chayama
Journal:  Clin J Gastroenterol       Date:  2009-07-28

5.  Clinicopathological features of liver injury in patients with type 2 diabetes mellitus and comparative study of histologically proven nonalcoholic fatty liver diseases with or without type 2 diabetes mellitus.

Authors:  Toshihide Shima; Hirofumi Uto; Kohjiro Ueki; Toshinari Takamura; Yutaka Kohgo; Sumio Kawata; Kohichiroh Yasui; Hyohun Park; Naoto Nakamura; Tatsuaki Nakatou; Nobuyoshi Tanaka; Atsushi Umemura; Masayuki Mizuno; Junko Tanaka; Takeshi Okanoue
Journal:  J Gastroenterol       Date:  2012-08-22       Impact factor: 7.527

6.  Entecavir and interferon-α sequential therapy in Japanese patients with hepatitis B e antigen-positive chronic hepatitis B.

Authors:  Masaru Enomoto; Shuhei Nishiguchi; Akihiro Tamori; Sawako Kobayashi; Hiroki Sakaguchi; Susumu Shiomi; Soo Ryang Kim; Hirayuki Enomoto; Masaki Saito; Hiroyasu Imanishi; Norifumi Kawada
Journal:  J Gastroenterol       Date:  2012-08-02       Impact factor: 7.527

  6 in total

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