Sixteen prepubertal patients with chronic renal failure (CRF) were given da
ily recombinant human growth hormone (rhGH) treatment (1.2 IU/kg per week)
for 2.6+/-1.6 years until kidney transplant. Therapy was then discontinued
and the patients followed for a further 3.5+/-1.4 years. During treatment,
mean height increased from -3.0+/-0.9 standard deviation score (SDS) to -1.
9+/-1.4 SDS (P<0.001) at the time of transplantation, corresponding to a me
an height gain of +1.2+/-0.9 SDS. After discontinuation of rhGH therapy, pr
epubertal children continued a partial catch-up growth with a height gain o
f +0.5+/-0.8 SDS for the follow-up period. Conversely, negative changes of
height were observed in pubertal transplanted children: -0.5+/-0.4 SDS in p
atients grafted at early stages of puberty (P2-P3) and -0.15+/-0.9 SDS in p
atients grafted at late stages of puberty (P4-P5). These data confirmed the
benefit of rhGH therapy in CRF patients. Nevertheless, only early initiati
on of rhGH treatment led some of these patients to their target height at t
ransplantation, thus preserving their potential growth. Reinitiation of rhG
H therapy after transplantation should be considered in order to complete c
atch-up growth to target height in prepubertal children.