Hepatitis C virus (HCV) infection is one of the major causes leading to ort
hotopic liver transplantation (OLT) worldwide, Although viral infection per
sists in almost all patients, the pathology of recurrent HCV infection afte
r OLT is not well characterized. To address this issue, we compared the pat
hological findings of 28 patients who underwent transplantation for HCV-rel
ated cirrhosis (group A, aged 47 +/- 15 years; 23 men, 5 women) with those
of 21 patients who underwent transplantation for nonviral indications (grou
p B, aged 45 +/- 21 years; 13 men; 8 women) during the first year after tra
nsplantation, Patients from group A were assessed for serum HCV RNA by 5' u
ntranslated region nested polymerase chain reaction before and 1 year after
OLT. Patients underwent protocol liver biopsies 3 months and 1 year after
transplantation. Group A patients more frequently had histological evidence
of hepatic steatosis than group B patients, both at 3 months (P = .003) an
d 1 year (P = .003) after OLT. Fibrosis and portal inflammation were statis
tically more frequent in group A 1 year after transplantation. The sensitiv
ity of steatosis in detecting histological disease recurrence was 100% at 3
months and 94% at 1 year; the specificity was 40% and 60%, respectively. C
onversely, steatosis was 100% specific in detecting viral recurrence, with
a sensitivity of 89%, The 1-year actuarial incidence of abnormal transamina
se levels was 52% in group A and 13% in group B (P = .05). No biochemical o
r histological differences between patients infected with genotype 1b and p
atients with other HCV genotypes were found. Hepatic steatosis is a specifi
c sign of viral recurrence after liver transplantation and a less specific
sign of disease recurrence. HCV-infected liver transplant recipients often
develop abnormal transaminase levels and liver fibrosis 1 year after OLT; t
hese features are unrelated to HCV genotypes, (C) 1998 by the American Asso
ciation for the Study of Liver Diseases.