BACKGROUND/AIMS: About 50% of patients with chronic hepatitis C do not resp
ond to interferon therapy and this failure is expensive. The aim of this st
udy was to identify possible predictive factors of biochemical non-response
during interferon therapy among biochemical, virological (HCV genotype), h
istological (Knodell's score) and pharmacokinetic (monoethylglycinexylidide
formation test) pretreatment parameters.
METHODOLOGY: Our study included 60 patients with chronic hepatitis C underg
oing a course of Interferon therapy. Patients whose serum ALT levels were n
ormal at the 3rd month of therapy and remained so until the end of treatmen
t were regarded as responders,
RESULTS: In univariate analysis, only the gamma-glutamyltransferase (gamma-
GT) and the gamma-GT/alanine aminotranferase ratio were significantly highe
r in non-responder patients. Multivariate logistic analysis showed that hig
h gamma-GT levels, high histological activity index, low monoethylglycinexy
lidide formation rate and viral genotype 1 were the best combination for th
e identification of non-responder patients (16.7% error rate). By adding al
anine aminotranferase modification at the Ist month of therapy the probabil
ity error was reduced to 5%.
CONCLUSIONS: These results show that the combination of biochemical, histol
ogical, virological and pharmacokinetic pre-treatment variables, associated
with alanine aminotranferase modification at the Ist month of therapy, can
predict non-response to interferon and allow therapeutic modifications.