INSULIN-LIKE GROWTH-FACTOR-I - CLINICAL-STUDIES

Citation
Pe. Vos et al., INSULIN-LIKE GROWTH-FACTOR-I - CLINICAL-STUDIES, Medicamentos de actualidad, 34(1), 1998, pp. 79-90
Citations number
89
Categorie Soggetti
Pharmacology & Pharmacy
Journal title
ISSN journal
00257656
Volume
34
Issue
1
Year of publication
1998
Pages
79 - 90
Database
ISI
SICI code
0025-7656(1998)34:1<79:IG-C>2.0.ZU;2-U
Abstract
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.