Insulin-like growth factor-I (IGF-I) has endocrine, autocrine and para
crine properties. Receptors for IGF-I are present on virtually all cel
l types but are located mainly on cells of mesenchymal origin, such as
fibroblasts, chondrocytes and osteoblasts. Growth hormone (GH)-depend
ent and GH-independent actions of IGF-I have been implicated in normal
and abnormal bone growth, diabetes mellitus, malnutrition, cancer, th
yroid disease and hematological diseases. The availability of recombin
ant human IGF-I (rhlGF-I) has led to new treatments for GH-resistant L
aron dwarfism and certain diseases associated with severe insulin resi
stance. IGF-I has recently been investigated as a neurotrophic factor.
Phase II efficacy trials with patients with neurological disease such
as traumatic brain injury, myotonic dystrophy and amyotrophic lateral
sclerosis have shown that rhlGF-I has efficacy on various outcome par
ameters. Treatment with rhlGF-I may result in reversible side effects
of which increased heart rate, papilledema, ophthalmologic and intracr
anial hypertension, facial and generalized edema, and weight gain are
noteworthy.