Treatment with direct-acting antivirals improves peripheral insulin sensitivity in non-diabetic, lean chronic hepatitis C patients

PLoS One. 2019 Jun 6;14(6):e0217751. doi: 10.1371/journal.pone.0217751. eCollection 2019.

Abstract

Background and aims: Hepatitis C virus (HCV) infection is associated with insulin resistance, which may lead to type 2 diabetes and its complications. Although HCV infects mainly hepatocytes, it may impair insulin sensitivity at the level of uninfected extrahepatic tissues (muscles and adipose tissue). The aim of this study was to assess whether an interferon-free, antiviral therapy may improve HCV-associated hepatic vs. peripheral insulin sensitivity.

Methods: In a single-arm exploratory trial, 17 non-diabetic, lean chronic hepatitis C patients without significant fibrosis were enrolled, and 12 completed the study. Patients were treated with a combination of sofosbuvir/ledipasvir and ribavirin for 12 weeks, and were submitted to a 2-step euglycemic hyperinsulinemic clamp with tracers, together with indirect calorimetry measurement, to measure insulin sensitivity before and after 6 weeks of antivirals. A panel of 27 metabolically active cytokines was analyzed at baseline and after therapy-induced viral suppression.

Results: Clamp analysis performed in 12 patients who achieved complete viral suppression after 6 weeks of therapy showed a significant improvement of the peripheral insulin sensitivity (13.1% [4.6-36.7], p = 0.003), whereas no difference was observed neither in the endogenous glucose production, in lipolysis suppression nor in substrate oxidation. A distinct subset of hepatokines, potentially involved in liver-to-periphery crosstalk, was modified by the antiviral therapy.

Conclusion: Pharmacological inhibition of HCV improves peripheral (but not hepatic) insulin sensitivity in non-diabetic, lean individuals with chronic hepatitis C without significant fibrosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antiviral Agents / therapeutic use*
  • Cytokines / blood
  • Diabetes Mellitus / pathology
  • Female
  • Glucose / metabolism
  • Hepatitis C, Chronic / blood
  • Hepatitis C, Chronic / drug therapy*
  • Humans
  • Insulin Resistance*
  • Male
  • Middle Aged
  • Thinness / complications*
  • Young Adult

Substances

  • Antiviral Agents
  • Cytokines
  • Glucose

Grants and funding

This work was supported by: (FN) Gilead Sciences, Inc. Foster City, CA, US, https://www.gilead.com/; Swiss National Science Foundation (314730-166609 to F.N.), http://www.snf.ch/en/Pages/default.aspx; FLAGS Foundation and the Fondation pour la Recherche sur le Diabète, Geneva, Switzerland, http://www.fondation-diabete.ch/. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.