Use of recombinant human growth hormone in children with chronic renal insufficiency: an update

B Lippe1, O Yadin, R N Fine

  • 1Department of Pediatrics, UCLA School of Medicine.

Hormone Research
|January 1, 1993
PubMed

Insights

Recombinant human growth hormone (rhGH) therapy significantly improves growth velocity in children with chronic renal failure (CRF). This treatment facilitates catch-up growth, addressing stunted growth common in pediatric CRF patients.

Area of Science:

  • Pediatric Nephrology
  • Endocrinology
  • Growth Hormone Therapy

Background:

  • Chronic renal insufficiency (CRI) frequently causes growth retardation in children.
  • Advancements in dialysis and transplantation highlight the need to address persistent short stature.
  • Recombinant human growth hormone (rhGH) is explored for growth enhancement in pediatric patients with chronic kidney disease (CKD).

Purpose of the Study:

  • To evaluate the efficacy of rhGH in promoting growth in children with chronic renal failure (CRF) before dialysis.
  • To assess changes in growth velocity (GV) and height standard deviation scores (SDS) during rhGH treatment.
  • To monitor for adverse effects and changes in renal function during rhGH therapy.

Main Methods:

  • Eleven male patients with CRF (ages 2.5-16.3 years) and height SDS > -2.0 were treated with rhGH.
  • Initial dosing: 0.125 mg/kg three times weekly; later changed to 0.053 mg/kg/day.
  • Treatment duration ranged from 18 to 48 months, with growth assessed at 12, 24, 36, and 48 months.

Main Results:

  • Mean growth velocity (GV) increased significantly from baseline (5.4 cm/year) to 8.9 cm/year at 12 months.
  • Mean height SDS improved from > -3.0 to < -1.5, with one patient reaching the 50th percentile.
  • No significant adverse effects or changes in creatinine clearance were observed; two patients initiated dialysis as expected for their condition.

Conclusions:

  • rhGH therapy effectively increases growth velocity in children with CRF.
  • rhGH facilitates catch-up growth, improving height deficits in this patient population.
  • The treatment appears safe and well-tolerated in children with CRF prior to dialysis.

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