Three years of GH treatment in Turner's syndrome: complex effect of GH dosage on growth parameters. French Pediatric Clinics and Sanofi-Winthrop

Clin Endocrinol (Oxf). 1996 Jun;44(6):665-71. doi: 10.1046/j.1365-2265.1996.697518.x.

Abstract

Objective: There have been few studies of GH dose responses in Turner's syndrome. We have therefore compared the growth effect of two doses of subcutaneous GH: 0.45 (D1) or 0.90 (D2) IU/kg/week.

Design: Multicentre study with two parallel randomized groups treated with D1 or D2 dose for one year, then with D2 for the second and third years in both groups.

Patients: Ninety-seven girls with Turner's syndrome aged from 4.8 to 16.5 years.

Results: The first mean height velocity (HV) was significantly higher with D2. At one year the girls changed from D1 to D2 showed a further acceleration in HV. During second and third years HV remained above the mean for untreated Turner girls, in both groups. Mean cumulative height gains over the 3 years were 1.06 and 1.17 SDS/CA (Ranke's Turner standard) in groups G1 and G2 respectively. Bone maturation, over 36 months, was 33.7 (G1) and 31.9 (G2) months.

Conclusion: These results suggest that, if a higher initial GH dose is associated with a greater net initial height gain, the duration of treatment might affect the long-term results. Intermittent treatment should be considered.

Publication types

  • Clinical Trial
  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial

MeSH terms

  • Adolescent
  • Body Height / drug effects*
  • Child
  • Child, Preschool
  • Drug Administration Schedule
  • Female
  • Growth Hormone / administration & dosage*
  • Growth Hormone / therapeutic use*
  • Humans
  • Injections, Subcutaneous
  • Recombinant Proteins / therapeutic use
  • Turner Syndrome / drug therapy*

Substances

  • Recombinant Proteins
  • Growth Hormone