Osteoporotic fractures and myopathies are disabling consequences of chronic glucocorticoid (GC) therapy. In vitro and in vivo, GCs inhibit osteoblast production of insulin-like growth factor I(IGF-I), a hormone known to promote collagen synthesis and cell replication in bone. GC therapy may also interfere with systemic action of IGF-I by increasing levels of a circulating IGF-I inhibitor. Negative GC effects on IGF-I production and action, therefore, appear to be important mechanisms by which GCs induce osteoporosis. Furthermore, GC therapy often results in muscle atrophy and weakness. IGF-I has been shown to have anabolic effects on skeletal muscle and may prevent the catabolic changes induced by GCs. The proposed studies will investigate the pathophysiology of GC effects upon bone and muscle and determine whether administration of IGF- I/BP-3 may prevent GC-induced osteoporosis and myopathy.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32DK010122-01
Application #
6208486
Study Section
Endocrinology Study Section (END)
Program Officer
Hyde, James F
Project Start
2000-09-01
Project End
Budget Start
2000-09-01
Budget End
2001-08-31
Support Year
1
Fiscal Year
2000
Total Cost
$42,628
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02199
Wilcox, Nicholas S; Rui, Jinxiu; Hebrok, Matthias et al. (2016) Life and death of ? cells in Type 1 diabetes: A comprehensive review. J Autoimmun 71:51-8