Mj. Contos et al., Development of nonalcoholic fatty liver disease after orthotopic liver transplantation for cryptogenic cirrhosis, LIVER TRANS, 7(4), 2001, pp. 363-373
Many subjects with cryptogenic cirrhosis have underlying nonalcoholic steat
ohepatitis (NASH), The natural history of NASH-related cryptogenic cirrhosi
s after orthotopic liver transplantation (OLT) is not well defined. A prima
rily retrospective study of patients with the clinical histological phenoty
pe of NASH-related cirrhosis undergoing OLT was performed. Data were compar
ed with 2 sets of age- and weight-matched controls with (1) primary biliary
cirrhosis or primary sclerosing cholangitis or (2) alcoholic liver disease
. After OLT, all patients were managed by a standard immunosuppressive prot
ocol. Liver biopsies were performed at 6 and 12 months after OLT and at 1-
to 2-year intervals thereafter, as well as when liver enzyme levels were el
evated enough to warrant diagnostic biopsy. Twenty-seven subjects with cryp
togenic cirrhosis and a clinical histological phenotype of NASH and 3 patie
nts with a long-standing diagnosis of NASH before OLT were included. The 30
-day perioperative mortality was 1 in 30 patients, During a median follow-u
p of 3.5 +/- 2.7 years, 2 additional patients died of sepsis, There was a t
ime-dependent increase in the risk for allograft steatosis that approached
100% by 5 years compared with only an approximately 25% incidence of steato
sis in the control groups (P < .009, log-rank test). On multivariate analys
is, only the cumulative steroid dose correlated with time to development of
allograft steatosis, Three patients developed histological progression fro
m hepatic steatosis to steatohepatitis, Of these, 1 patient developed progr
essive fibrosis. Four patients experienced at least 1 episode of acute cell
ular rejection; however, no patient developed chronic rejection or graft fa
ilure. In conclusion, nonalcoholic fatty liver disease occurs frequently af
ter OLT in patients with the phenotype of NASH-related cirrhosis. Despite t
he frequent histological recurrence of disease, clinical outcomes are simil
ar to those of other groups of patients undergoing OLT.