After a decade of experience with recombinant human growth hormone (rhGH) i
n children with chronic renal failure (CRF), the long-term efficacy and saf
ety of the drug is now established. In prepubertal children, partial catch-
up growth is achieved during the first three treatment years, followed by s
ustained percentile-parallel growth. Discontinuation of rhGH treatment resu
lts in catch-down growth in 75% of patients. Treatment efficacy is inversel
y correlated with age and baseline height velocity, and positively influenc
ed by genetic target height and residual renal function. Skeletal maturatio
n is not accelerated, suggesting a true increase in final height potential.
Side effects are limited to a stimulation of insulin secretion, which is n
ot associated with changes in glucose tolerance, and occasional cases of be
nign intracranial hypertension.
In summary, the advent of rhGH has opened a new era in the management of gr
owth failure in CRF. Available evidence suggests that treatment should star
t in early childhood and early in the course of renal failure, and should b
e continued at least until renal transplantation. It remains to be seen whe
ther the beneficial effect of rhGH on height observed during the prepuberta
l period will result in an eventual increase in adult height.