Thalassemic patients today undergo intensive transfusion and chelation regi
mes that offer them prolonged survival and improved quality of life. Nevert
heless, they face the consequences of chronic illness and therapies which a
ffect multiple bodily functions. Endocrine derangements involve, among othe
rs, the GB-IGF-I axis with consequent impairment of growth. In such cases,
GH release, as assessed with stimulation tests, may be normal whereas ultra
dian GH secretion seems to be subnormal. New GH secretagogues (GHRs) are ag
ents that stimulate pituitary GH release by acting upon different receptors
than the endogenous hypothalamic secretagogue, growth hormone-releasing ho
rmone (GHRH). Examples are the growth hormone releasing peptides (GHRPs) GH
RP-6, GHRP-1, GHRP-2, Hexarelin and the non-peptidyl MK-0677, These can be
administered by multiple routes, even per os or intranasally, thus obviatin
g the need for injections. Their Ga releasing capacity is more pronounced a
nd prolonged than that of GHRH and their use is devoid of serious side effe
cts. The most recently developed GHRs seem to be capable of producing susta
ined GH release in many cases and can thus be viewed as therapeutic candida
tes in cases of reduced GH secretion with intact pituitary, as seems to be
the case in a group of thalassemic patients.