Literature DB >> 26192429

Ursodeoxycholic acid exacerbates peginterferon-induced interstitial pneumonia in a patient with hepatitis C.

Rena Kaneko1, Masazumi Ogawa2, Tomoyuki Iwata2, Yasuyoshi An2, Motoki Nakagawa2, Satoshi Kusayanagi2, Satoshi Kamisago2, Tomoyuki Umeda2, Yuzuru Sato2.   

Abstract

Pegylated interferon alpha combined with ribavirin is currently the standard treatment for hepatitis C virus (HCV) infection. Ursodeoxycholic acid (UDCA) is used as a complementary treatment in patients who are non-responders or who develop severe side effects of this combined therapy. UDCA is generally considered to be a relatively safe drug. However, we recently encountered a patient with chronic hepatitis C in whom interferon-induced interstitial pneumonia was exacerbated by UDCA. This patient responded to initial antiviral therapy with non-pegylated interferon alpha-2b and ribavirin, but hepatitis recurred soon after the end of treatment. A second course of antiviral therapy using peginterferon alpha-2b and ribavirin achieved normalization of serum transaminases and HCV-RNA, but also caused interstitial pneumonia. After discontinuing peginterferon, this side effect was ameliorated. On the other hand, hepatitis relapsed four months later. UDCA treatment was started and serum transaminase levels decreased, but exacerbation of interstitial pneumonia occurred with marked elevation of the serum KL-6 level. To our knowledge, this is the first reported case of peginterferon-induced interstitial pneumonia showing exacerbation due to UDCA therapy.

Entities:  

Keywords:  Hepatitis C; Interstitial pneumonia; Peginterferon; Ribavirin; Ursodeoxycholic acid

Year:  2009        PMID: 26192429     DOI: 10.1007/s12328-009-0075-y

Source DB:  PubMed          Journal:  Clin J Gastroenterol        ISSN: 1865-7265


  15 in total

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10.  Virological response in patients with hepatitis C virus genotype 1b and a high viral load: impact of peginterferon-alpha-2a plus ribavirin dose reductions and host-related factors.

Authors:  Gotaro Yamada; Shiro Iino; Tadao Okuno; Masao Omata; Kendo Kiyosawa; Hiromitsu Kumada; Norio Hayashi; Takahiro Sakai
Journal:  Clin Drug Investig       Date:  2008       Impact factor: 2.859

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