E. Giannini et al., Steatosis and bile duct damage in chronic hepatitis C: distribution and relationships in a group of Northern Italian patients, LIVER, 19(5), 1999, pp. 432-437
Background/Aims: Hepatitis C virus (HCV) related disease follows a long, be
nign course and most affected patients have mild disease. Liver biopsy is m
andatory to grade and stage the disease. Characteristic, though non-specifi
c, HCV histological lesions such as bile duct damage and steatosis have bee
n singled out but their association with non-histological parameters has no
t been completely defined. Our aim was to study the relationships among the
se histological lesions and clinical, biochemical, functional and virologic
al characteristics in a group of Northern Italian patients with chronic hep
atitis. Methods: We studied 172 patients with HCV-related chronic hepatitis
. Patients were divided into groups on the basis of histology including bil
e duct damage and steatosis. Clinical, biochemical, functional and virologi
cal profiles were related to histological findings. Results: Histological g
rading and staging of disease increased as the age of patients increased. S
teatosis was present in 70% of our patients and was related to a higher deg
ree of fibrosis and to decreased functional activity. The prevalence of bil
e duct damage was 20%. This lesion was present in older patients with highe
r staging and impaired liver function. Biochemically it was associated with
an increase in aspartate aminotransferase, gammaglutamyltranspeptidase, al
kaline phosphatase, and total bilirubin. Conclusions: In the population we
studied, HCV chronic hepatitis was predominantly a mild disease. Moreover b
oth steatosis and bile duct damage were also mild. Steatosis was associated
with fibrosis and this might influence liver metabolic function. Bile duct
lesions were found in older patients with advanced disease showing biochem
ical evidence of cholestasis. The molecular role HCV might play in the path
ogenesis of these histological features should be addressed in further stud
ies.