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Serum asunaprevir concentrations showing correlation with the extent of liver fibrosis as a factor inducing liver injuries in patients with genotype-1b hepatitis C virus receiving daclatasvir plus asunaprevir therapy

Author

Listed:
  • Yoshihito Uchida
  • Kayoko Naiki
  • Jun-ichi Kouyama
  • Kayoko Sugawara
  • Masamitsu Nakao
  • Daisuke Motoya
  • Mie Inao
  • Nobuaki Nakayama
  • Yukinori Imai
  • Tomoaki Tomiya
  • Satoshi Mochida

Abstract

Aims: Liver injury can occur during antiviral therapies with direct-acting antivirals (DAAs), potentially necessitating discontinuation of the therapies, with consequent worsening of the sustained viral response (SVR) rates, in patients with hepatitis C virus (HCV). To clarify the mechanisms involved in serum transaminase level elevation, we performed a retrospective evaluation of the serum concentrations of daclatasvir and asunaprevir, both classified as DAAs, in patients receiving treatment with a combination of the two drugs. Methods: Subjects were 278 Japanese patients with genotype-1b HCV who received daclatasvir plus asunaprevir therapy for more than 4 weeks. Serum concentrations of both the DAAs were measured at 4 weeks after the initiation of therapy. Result: Liver injuries including serum AST and/or ALT level elevation to 150 U/L or over were found in 34 patients (12.2%). Multivariate logistic regression analysis identified serum asunaprevir concentrations as being significantly associated with developing liver injury, with an odds ratio of 1.046 (95% confidence interval 1.011–1.082, p

Suggested Citation

  • Yoshihito Uchida & Kayoko Naiki & Jun-ichi Kouyama & Kayoko Sugawara & Masamitsu Nakao & Daisuke Motoya & Mie Inao & Nobuaki Nakayama & Yukinori Imai & Tomoaki Tomiya & Satoshi Mochida, 2018. "Serum asunaprevir concentrations showing correlation with the extent of liver fibrosis as a factor inducing liver injuries in patients with genotype-1b hepatitis C virus receiving daclatasvir plus asu," PLOS ONE, Public Library of Science, vol. 13(10), pages 1-13, October.
  • Handle: RePEc:plo:pone00:0205600
    DOI: 10.1371/journal.pone.0205600
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