Ac. Moses, RECOMBINANT HUMAN INSULIN-LIKE-GROWTH-FACTOR AS A THERAPEUTIC AGENT FOR SEVERE INSULIN-RESISTANCE AND TYPE-II DIABETES-MELLITUS, Journal of pediatric endocrinology & metabolism, 10, 1997, pp. 123-130
Recombinant human insulin-like growth factor I (rhIGF-I) shares many p
hysiological properties with its structural homolog insulin. Studies i
n normal humans have confirmed the hypoglycemic potential of exogenous
rhIGF-I and have provided a rationale for the testing of rhIGF-I as a
potential therapy in states of severe insulin resistance and in type
II diabetes mellitus. These studies have demonstrated that rhIGP-I can
improve hyperglycemia, hyperinsulinemia and insulin sensitivity in su
bjects with severe insulin resistance and that it can improve glycemic
control and insulin sensitivity in patients with type II diabetes mel
litus. Data are accruing that rhIGF-I can also improve hypertriglyceri
demia associated with these insulin resistant states. While early stud
ies have revealed significant side effects of rhIGF-I at doses greater
than 90 mu g/kg b.i.d., more recent preliminary data suggest that eff
icacious doses with good patient tolerance can be identified.