Penal failure is characterized by endocrine and metabolic disorders, s
ome of them being described as a state of resistance to growth hormone
(GH) and/or insulin-like growth factor (IGF) 1. There is evidence for
a reduced metabolic action of IGF-1 (formerly somatomedin C) in hemod
ialysis and kidney transplant children and in adults undergoing hemodi
alysis. Since the development of recombinant human (rh) IGF-1, despite
strong metabolic actions, some experimental studies suggest a decreas
e in metabolic effects of rhIGF-1 in chronic renal failure (CRF). Prel
iminary reports in adult dialysis patients also stressed the possibili
ty of a resistance to rhIGF-1 metabolic actions. The perturbed IGF-bin
ding protein system in CRF may play an important role in modifying sto
rage and IGF-I delivery to tissues. Also, by analogy with insulin, rec
eptor and postreceptor defects may be involved in this condition, as s
uggested by rhIGF-1 resistance with aging or in obese Zucker rats. How
ever, rhIGF-1 remains a potent anabolic factor in uremia. Further stud
ies will therefore be necessary to clarify this IGF-1 resistance state
. Such knowledge might allow physicians to reduce the amount of rhIGF-
1 administered to the patients and improve the anabolic actions of rhI
GF-1 during acute and chronic renal failure.