Biological mechanisms of depression following treatment with interferon for chronic hepatitis C: A critical systematic review

J Affect Disord. 2017 Feb:209:235-245. doi: 10.1016/j.jad.2016.11.039. Epub 2016 Nov 27.

Abstract

Background: A significant subset of patients infected by the hepatitis C virus (HCV) develops a major depressive episode (MDE) during Interferon-alpha (IFN-α) based immunotherapy. We performed a systematic review of studies which examined biological mechanisms contributing to the onset of a MDE during IFN-α-based immunotherapy for HCV.

Methods: Major electronic databases were searched from inception up until 15th February 2016 for peer-reviewed prospective studies that had enrolled HCV infected patients who received IFN-α treatment. A diagnosis of MDE had to be established by means of a standardized diagnostic interview at baseline and endpoint.

Results: Eight unique references met inclusion criteria. A total of 826 participants with HCV (37.3% females, mean age 46.7 years) were included in this systematic review. The overall MDE incidence rate was 34.8%, with follow-up ranging between 4 and 48 weeks. The methodological quality varied across selected studies. It was observed that Interleukin-6, salivary cortisol, arachidonic acid / eicosapentaenoicacid plus docosahexaenoic acid ratio, and genetic polymorphisms may present variations which are linked to a predisposition to INF-α-induced depression.

Limitations: A meta-analysis could not be performed due to the diverse biological mechanisms investigated and the lack of replicated evidence.

Conclusions: This systematic review indicates that several potential mechanisms may be implicated in the onset of a MDE following IFN-α-based immunotherapy for chronic HCV. However, replicated evidence is lacking and therefore the mechanisms involved in IFN-α-induced depression in humans remain unclear.

Keywords: Depression; Hepatitis C; Inflammation; Interferon-alpha; Psychoneuroimmunology.

Publication types

  • Review
  • Systematic Review

MeSH terms

  • Adult
  • Antiviral Agents / adverse effects*
  • Antiviral Agents / therapeutic use
  • Depression / blood
  • Depression / chemically induced*
  • Depression / genetics
  • Female
  • Genetic Predisposition to Disease
  • Hepatitis C, Chronic / drug therapy*
  • Humans
  • Interferon-alpha / adverse effects*
  • Interferon-alpha / therapeutic use
  • Interleukin-6 / blood
  • Male
  • Middle Aged
  • Prospective Studies

Substances

  • Antiviral Agents
  • IL6 protein, human
  • Interferon-alpha
  • Interleukin-6