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Published on: September 1, 2016
Effects of growth hormone on growth factors after renal transplantation
J P Clot1, H Crosnier, G Guest
1INSERM U530, Hôpital des Enfants Malades, 149 rue de Sèvres, 75743 Paris Cedex 15, France.
Insights
Growth hormone (GH) therapy improved growth in renal transplanted children, increasing insulin-like growth factor-1 (IGF-1) and IGF binding protein-3 (IGFBP-3). However, corticosteroid use may cause IGF-1 insensitivity, limiting optimal growth response.
Area of Science:
- Pediatric Endocrinology
- Nephrology
- Growth Hormone Therapy
Background:
- Growth retardation is common in children post-renal transplantation (RTx).
- Growth hormone (GH) treatment can potentially improve growth in these patients.
- Understanding the IGF-1/IGFBP axis is crucial for assessing treatment efficacy.
Purpose of the Study:
- To evaluate the IGF-1 and IGFBP profile in growth-retarded children after renal transplantation during GH therapy.
- To assess the impact of GH treatment on growth parameters and the IGF system.
- To investigate potential factors contributing to suboptimal growth response.
Main Methods:
- Retrospective analysis of ten prepubertal children with RTx and growth retardation.
- Administration of recombinant human GH (4 IU/m2/day) for one year.
- Measurement of plasma GH, total and free IGF-1, IGFBP-2, and IGFBP-3 using radioimmunoassay (RIA), SDS-PAGE, ligand, and immunoblot analyses.
Main Results:
- Significant increase in growth velocity (SD score for bone age) after GH therapy (P < 0.01).
- Doubled plasma levels of total and free IGF-1 (P < 0.01).
- Increased IGFBP-3 concentrations by approximately 40% (P < 0.01), with no change in IGFBP-2.
Conclusions:
- GH therapy effectively increases IGF-1 and IGFBP-3 levels in children with RTx.
- The observed growth response suggests potential IGF-1 insensitivity, possibly linked to corticosteroid use.
- Further research is needed to optimize GH therapy in this patient population.
Abstract:
Growth retardation occurs frequently in renal transplanted children (RTx) and can be improved by growth hormone (GH) treatment. This study retrospectively examines the insulin-like growth factor-1 (IGF-1) and IGF binding protein (IGFBP) profile of ten growth-retarded children previously given renal allografts, after 1 year of GH treatment period. Ten prepubertal patients (nine boys and one girl) were investigated. They had a mean chronological age (CA) of 11.4 +/- 1.1 years and a mean bone age (BA) of 7.3 +/- 0.9 years. Mean height was -3.9 +/- 0.4 SD units below the mean for CA. The mean body mass index (BMI) was 16.9 +/- 0.6 and the mean inulin clearance was 36.5 +/- 4.9 ml/min/1.73 m2. Recombinant hGH was given at 4 IU/m2/day. Plasma GH, total and free IGF-1, IGFBP-2 and -3 were measured by specific radioimmunoassay (RIA). IGFBPs were characterized by SDS PAGE techniques and ligand and immunoblot analyses. Mean velocity was markedly increased (P < 0.01) after 1 year of GH therapy, expressed as SD score for BA. The range of growth response was wide. The total and free plasma IGF-1 increased (P < 0.01) by about 100% (mean values after GH therapy: 95.9 +/- 2.1 nM and 165 +/- 29 pM, respectively). Plasma IGFBP-3 concentrations increased by about 40% (mean value: 148 +/- 18 pM, P < 0.01), with a concomitant increase in both intact IGFBP-3 and its 30-kDa proteolytic fragment. There was no change in plasma IGFBP-2 concentration. Both mean values of inulin clearance and BMI were unchanged during the treatment. In view of the IGF-1/IGFBP concentration changes, there should have been an even better growth response to GH therapy in these patients. This strongly suggests IGF-1 insensitivity, probably as a result of corticosteroid therapy.
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