Growth hormone treatment in children with preterminal chronic renal failure: no adverse effect on glomerular filtration rate

Eur J Pediatr. 1992 Aug;151(8):601-7. doi: 10.1007/BF01957731.

Abstract

Impaired growth and stunting remains a major therapeutic problem in children with chronic renal failure (CRF). Recombinant human growth hormone (rhGH) treatment may be beneficial, but concern has been raised about possible side-effects, i.e. deterioration of renal function and glucose intolerance. We have treated 10 prepubertal children with CRF (median age 7.5 [1.7-10.0] years) with 4 IU rhGH/m2 per day s.c. over a period of 1 year. Height velocity increased significantly (P less than 0.03) from basal 4.6 (2.0-14.0) cm/year to 9.7 (6.8-17.6) cm/year. Height velocity SDS for chronological age and for bone age increased in all children from basal median -2.3 to +3.8 (P less than 0.005). Median glomerular filtration rate (GFR) measured by single injection inulin clearance at onset was 18 (11-66) ml/min per 1.73 m2 and did not change significantly during the treatment year. The loss of GFR as estimated by creatinine clearance was similar during the treatment year (median loss 1.3 ml/min per 1.73 m2) compared to the year before treatment (median loss 3.7 ml/min per 1.73 m2). Serum glucose levels during an oral glucose tolerance test did not change, but fasting as well as stimulated insulin levels increased significantly with time during the study period. It is concluded that the rhGH regimen employed was remarkably effective in improving growth velocity in children with CRF without adversely affecting GFR. Glucose homeostasis remained stable, but at the expense of increased serum insulin levels.

MeSH terms

  • Blood Glucose / analysis
  • Carrier Proteins / analysis
  • Child
  • Child, Preschool
  • Female
  • Glomerular Filtration Rate*
  • Growth
  • Growth Disorders / blood
  • Growth Disorders / drug therapy*
  • Growth Disorders / etiology
  • Growth Hormone / adverse effects
  • Growth Hormone / therapeutic use*
  • Humans
  • Infant
  • Insulin-Like Growth Factor Binding Proteins
  • Insulin-Like Growth Factor I / analysis
  • Insulin-Like Growth Factor II / analysis
  • Kidney Failure, Chronic / blood
  • Kidney Failure, Chronic / complications*
  • Kidney Failure, Chronic / physiopathology
  • Male
  • Recombinant Proteins / therapeutic use
  • Somatomedins / analysis
  • Urea / blood

Substances

  • Blood Glucose
  • Carrier Proteins
  • Insulin-Like Growth Factor Binding Proteins
  • Recombinant Proteins
  • Somatomedins
  • Insulin-Like Growth Factor I
  • Insulin-Like Growth Factor II
  • Urea
  • Growth Hormone