Successful antiviral therapy is associated with a decrease of serum prohepcidin in chronic hepatitis C

World J Gastroenterol. 2010 Apr 14;16(14):1747-52. doi: 10.3748/wjg.v16.i14.1747.

Abstract

Aim: To assess serum concentrations of prohepcidin in chronic hepatitis C individuals and evaluate their associations with disease activity and efficacy of pegylated interferon (PEG-IFN)/ribavirin (RBV) therapy.

Methods: Prohepcidin was measured in sera of 53 chronic hepatitis C patients. Concentrations of prohepcidin and other iron metabolism markers were analyzed at 9 time points before, during and after the end of antiviral therapy.

Results: In hepatitis C virus (HCV) genotype 1-infected individuals, a gradual decrease of prohepcidin during antiviral therapy was observed in responders (88.8 +/- 14.7 ng/mL before therapy vs 60.6 +/- 0.3 ng/mL in the 48th wk, P = 0.04). In contrast, no decrease was observed in non-responders. A similar association was observed in HCV genotype 3a individuals, with a statistically significant decline in serum prohepcidin only in the responder group (99.5 +/- 5.2 ng/mL at baseline vs 72.7 +/- 6.1 ng/mL in the 24th wk, P = 0.01). Moreover, HCV-RNA at week 12 of therapy was positively correlated with baseline (R = 0.63, P < 0.005) and week 12 (R = 0.60, P = 0.01) serum prohepcidin concentrations in HCV genotype 1 infection.

Conclusion: Successful PEG-IFN/RBV therapy results in a decline of serum prohepcidin concentration in chronic hepatitis C, which may suggest a direct effect of HCV on iron metabolism at the prohormonal level of hepcidin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antimicrobial Cationic Peptides / blood*
  • Antiviral Agents / therapeutic use*
  • Female
  • Hepatitis C, Chronic / blood*
  • Hepatitis C, Chronic / drug therapy*
  • Hepatitis C, Chronic / metabolism
  • Hepcidins
  • Humans
  • Interferon alpha-2
  • Interferon-alpha / therapeutic use
  • Iron / metabolism
  • Male
  • Middle Aged
  • Polyethylene Glycols / therapeutic use
  • Protein Precursors / blood*
  • Recombinant Proteins
  • Ribavirin / therapeutic use
  • Young Adult

Substances

  • Antimicrobial Cationic Peptides
  • Antiviral Agents
  • Hepcidins
  • Interferon alpha-2
  • Interferon-alpha
  • Protein Precursors
  • Recombinant Proteins
  • Polyethylene Glycols
  • Ribavirin
  • Iron
  • peginterferon alfa-2a