Serum immunoglobulins predict the extent of hepatic fibrosis in patients with chronic hepatitis C virus infection

K. Watt, J. Uhanova, Y. Gong, K. Kaita, K. Doucette, N. Pettigrew, G. Y. Minuk

Research output: Contribution to journalReview articlepeer-review

33 Scopus citations

Abstract

Recently, we documented that immunoglobulins stimulate the proliferative activity of rat hepatic stellate cells in vitro. The aim of the present study was to determine whether there is any association between serum immunoglobulin levels and hepatic fibrosis in patients with chronic hepatitis C virus (HCV) infection. Charts from 116 patients with biochemical, serologic, virologic and histologic evidence of chronic hepatitis C infection and serum immunoglobulin levels (IgA, IgG, IgM and total) were reviewed. The mean (±SD) age of the study population was 46 ± 11 years and 67 (58%) were male. There were significant correlations between serum IgA (r = 0.39, P = 0.00001), IgG (r = 0.49, P = 0.000002) and total (r = 0.51, P = 0.000003) immunoglobulin levels and the stage of hepatic fibrosis. When serum immunoglobulin levels were included into logistic regression analysis with variables known to be associated with advanced disease (male gender, age >40 years at onset of infection, duration of infection beyond 20 years and concurrent alcohol abuse) only IgA, IgG and total immunoglobulin levels (P < 0.05, <0.05 and <0.005, respectively) emerged as independent predictors of hepatic fibrosis. Our data indicate a strong association between serum immunoglobulin levels (IgA, IgG and total) and hepatic fibrosis in patients with HCV infection. This finding supports the need to further investigate whether immunoglobulins independently promote disease progression in patients with chronic HCV infection.

Original languageEnglish (US)
Pages (from-to)251-256
Number of pages6
JournalJournal of viral hepatitis
Volume11
Issue number3
DOIs
StatePublished - May 2004

Keywords

  • Cirrhosis
  • Fibrogenesis
  • Hepatic stellate cells
  • Hepatitis C virus
  • Immunoglobulins
  • Inflammation
  • Liver disease
  • Myofibroblasts

ASJC Scopus subject areas

  • Hepatology
  • Infectious Diseases
  • Virology

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