Various studies have evaluated the usefulness of measuring insulin-like gro
wth factor I (IGF-I) and IGF-binding proteins, compared with growth hormone
(GH), in the diagnosis and follow-up of patients with acromegaly. The clin
ical use of recently developed, highly sensitive GH assays has improved our
understanding of the secretion of GH at very low concentrations. Studies e
xamining the GH nadir after oral glucose administration in healthy adults s
uggest that GH values should be suppressed to no more than 0.14 mu g/l afte
r oral glucose administration. The highly sensitive GH assays are now being
used in the diagnosis of patients with acromegaly and in post-treatment fo
llow-up. In addition, the use of IGF-I immunoassays has confirmed that seru
m IGF-I level is a reliable and useful biochemical marker for determining G
H excess. The widespread use of highly sensitive, carefully validated assay
s offers accurate and reproducible biochemical information that will help i
n the overall clinical management of patients with acromegaly, including th
e monitoring of disease remission, disease cure and treatment titration reg
imen, as well as the early recognition of patients with residual disease. (
C) 2000 Harcourt Publishers Ltd.