Abstract
Insulin-like growth factor-I (IGF-I) is one of the most important regulator of growth. IGF-I deficiency is associated with prenatal and post- natal growth failure and may arise primarily as a result of GH receptor/post- receptor abnormalities or defects in the synthesis and transport of IGF-I. We have previously reported a 17.2 year-old boy with severe growth retardation and undetectable serum levels of IGF-I caused by a partial deletion of the IGF-I gene. This short review will concentrate on results of a recent study which examined the effects of rhlGF-I therapy on the GH-IGF system of this patient. Similar to healthy individuals, this patient had normal IGFBP-3 but elevated ALS levels. IGF-I treatment has improved linear growth and insulin sensitivity in this patient by restoring IGF-I levels and by normalizing circulating GH, IGFBPs and insulin levels.
Original language | English (US) |
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Pages (from-to) | 47-52 |
Number of pages | 6 |
Journal | Growth Hormone and IGF Research |
Volume | 9 |
Issue number | SUPPL. B |
DOIs | |
State | Published - Jan 1 1999 |
Externally published | Yes |
Keywords
- ALS
- IGF-Binding Proteins
- IGF-I gene deletion
- RhlGF-I
ASJC Scopus subject areas
- Endocrinology, Diabetes and Metabolism
- Endocrinology