A two year observation of the process of applying recombinant IGF-1 to treat short stature in children with primary IGF-1 deficiency -- case reports of 3 patients

Pediatr Endocrinol Diabetes Metab. 2011;17(4):233-8.

Abstract

Growth deficiency is one of the most frequent causes of referral to Endocrinology Outpatient Clinic. IGF-1 (insulin-like growth factor 1) deficiency is one of the rarest causes of short stature. In 2009 in Poland a therapeutic programme was set up for children with severe primary IGF-1 deficiency. The authors present the data of three first polish patients qualified for the rhIGF-1 (recombinant human insulin-like growth factor 1) - mecasermin. The authors conclude that the treatment with rhIGF-1 significantly improves growth velocity in patients with IGF-1 deficiency. During two years of mecasermin treatment no serious side effects were noted.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Body Height / drug effects
  • Child
  • Dose-Response Relationship, Drug
  • Female
  • Follow-Up Studies
  • Growth Disorders / blood*
  • Growth Disorders / drug therapy*
  • Humans
  • Insulin-Like Growth Factor I / deficiency*
  • Insulin-Like Growth Factor I / therapeutic use
  • Intercellular Signaling Peptides and Proteins / administration & dosage*
  • Male
  • Recombinant Proteins / therapeutic use
  • Treatment Outcome

Substances

  • Intercellular Signaling Peptides and Proteins
  • Recombinant Proteins
  • myotrophin
  • Insulin-Like Growth Factor I