From 1991 to 1993, 90 children having received a kidney graft with a p
ost-transplantation period of at least 12 months were included in a pr
ospective study carried out in Is French pediatric centers. After info
rmed consent and randomization, children received recombinant human gr
owth hormone (rhGH) (Genotonorm, Pharmacia peptide hormones) 30 U/m(2)
per week, either immediately on enrollment, for the treated group, or
after 1 year of follow-up for the group serving as a control. After 1
year both groups were treated and we analyzed data during the subsequ
ent years. Eighty-five children completed the 1-year study. Growth vel
ocity was significantly increased by rhGH: 7.7 cm with a gain of +0.3
standard deviation score in the treated group versus 3.6 cm in the con
trol group (P<0.0001) during the Ist year. Four factors predicted resp
onse to therapy: growth velocity prior to GH therapy, glomerular filtr
ation rate (GFR) at the start, mode of corticosteroid administration,
and degree of insulin resistance. After I year we observed a moderate,
significant decrease in GFR in both groups. Biopsy-proven acute rejec
tion episodes were not significantly more frequent during the Ist year
in the group of patients who received rhGH: 9 in 44 versus 4 in 46 pa
tients. The patients who rejected did not differ in terms of age, rena
l function at the start, and type of immunosuppression, but history of
rejection before GH treatment was discriminatory: 6 of 17 children wi
th two or more episodes had a new rejection versus 1 of 22 who had no
or only one episode (P=0.01). Glucose tolerance was not modified after
1 year of GH therapy. During the subsequent years of treatment a decr
ease in growth velocity was noted: 5.9 cm at 2 years, 5.5 at 3 years,
and 5.2 cm at 4 years. In conclusion, GH is efficient for improving gr
owth velocity in short transplanted children, inducing clear-cut but l
imited catch-up growth. The risk of rejection was shown only in patien
ts with a prior history of more than one rejection episode.