The administration of rhIGF-I in appropriate doses leads to a decrease
of insulin and growth hormone secretion and to an increase of insulin
sensitivity. In type 2 diabetic patients, IGF-I improves glycemic pro
files. In normal subjects, IGF-I increases energy expenditure and lipi
d oxidation and has a protein-sparing effect. Total and VLDL-triglycer
ides as well as LDL-cholesterol are decreased by IGF-I administration.
This metabolic profile of IGF-I allows speculation on its possible us
efulness in conditions of relative insulin resistance often associated
with increased cardiovascular morbidity and mortality.