Background: Occasional and transient increase in liver enzymes is reported
during growth hormone (GH) treatment in girls with Turner syndrome (TS).
Methods: Retrospectively, the specific role of GH treatment on liver and mu
scular enzymes was evaluated in 78 patients (48 boys; age range 4.0-20.8 ye
ars) affected by GH deficiency (GHD) who had been treated with GH for at le
ast 1 year (range: 1-15 years). All patients had normal serum levels of liv
er and muscular enzymes before GH therapy was started.
Results: A clinically asymptomatic and mild increase in serum transaminase
levels was observed in 6 of 78 patients with GHD during GH treatment; 3 (3.
8%) of the patients showed an isolated, transitory and self-limiting increa
se in serum liver transaminase levels which was noticed 6 to 12 months afte
r GH treatment was started, and normalized spontaneously within 3 to 6 mont
hs, without stopping the therapy. Three additional patients showed a transi
tory mild increase both in aspartate aminotransferase (AST) and creatine ph
osphokinase (CK) which also normalized spontaneously within 3 to 6 months.
The increase in transaminase levels was not related to the brand of GH prep
arations nor to the dosage administered.
Conclusions: A mild, transient, self-limiting increase in serum transaminas
e may occur during GH treatment. Concomitant determination of CK serum leve
ls may quickly differentiate muscular from hepatic hypertransaminasemia. Ex
cept for persistent cases, this condition does not generally require furthe
r investigations.