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Early recombinant human growth hormone treatment in glucocorticoid-treated children with juvenile idiopathic
Dominique Simon1, Anne-Marie Prieur, Pierre Quartier
1Department of Pediatric Endocrinology, Robert Debré Teaching Hospital, 75019 Paris, France. dominique.simon@rdb.aphp.fr
Insights
Early recombinant human growth hormone (rhGH) therapy in children with juvenile idiopathic arthritis (JIA) preserved normal growth velocity and height. Carbohydrate metabolism requires close monitoring during rhGH treatment.
Area of Science:
- Pediatric Endocrinology
- Rheumatology
- Growth Hormone Therapy
Background:
- Long-term glucocorticoid therapy negatively impacts growth and body composition in children with juvenile idiopathic arthritis (JIA).
- Previous studies indicated recombinant human growth hormone (rhGH) could halt these complications without causing catch-up growth.
Purpose of the Study:
- To evaluate the impact of early rhGH initiation on growth and body composition in children with JIA.
- To assess adverse effects associated with rhGH therapy in this pediatric population.
Main Methods:
- A 3-year randomized controlled study involving 30 children with JIA undergoing glucocorticoid therapy.
- Participants received daily subcutaneous injections of rhGH (n=15) or no rhGH therapy (n=15).
- Evaluated outcomes included height standard deviation score (SDS) change, height velocity, body composition, and oral glucose tolerance.
Main Results:
- rhGH treatment resulted in a significantly larger increase in height SDS compared to the control group (P=0.04).
- Height velocity normalized within the first year of rhGH treatment and was maintained.
- Patients receiving rhGH showed greater increases in lean mass (P=0.03), while fat mass and bone mineralization remained comparable between groups.
Conclusions:
- Early initiation of rhGH in children with JIA effectively preserves normal growth velocity and height.
- rhGH was generally well-tolerated, but close monitoring of carbohydrate metabolism is recommended.
Context:
Long-term glucocorticoid therapy adversely affects growth and body composition in children with juvenile idiopathic arthritis (JIA). In previous studies, recombinant human GH (rhGH) halted the progression of these complications without inducing catch-up growth.
Objectives:
The objective of the study was to evaluate the impact on growth and body composition of rhGH started early after glucocorticoid initiation and to record adverse effects in children with JIA.
Design:
This is a 3-yr randomized controlled study.
Setting:
This study was conducted in a teaching hospital.
Patients:
Thirty children, 12-15 months into glucocorticoid therapy for severe JIA, were enrolled.
Intervention:
Patients received rhGH (0.46 mg/kg.wk) in daily sc injections (n = 15) or no rhGH therapy (n = 15) for 3 yr.
Main Outcome Measure:
Difference in height sd score (SDS) change between the two groups was assessed. Height velocity, body composition, and oral glucose tolerance were evaluated yearly.
Results:
Mean height SDS increase was larger with rhGH (+0.37 +/- 1.5 SDS) than without (-0.96 +/- 1.2 SDS) (P = 0.04). Mean height velocity returned to normal within the first year of rhGH treatment and remained normal thereafter. Mean lean mass increase was greater with rhGH treatment (+7.3 +/- 2.9 kg vs. +4.4 +/- 2.8 kg; P = 0.03). Fat mass and bone mineralization were not significantly different in the two groups. Fasting serum insulin increased significantly in rhGH-treated patients (5.2 +/- 16 mIU/liter) compared with untreated controls (-2.3 +/- 5 mIU/liter) (P = 0.04); fasting glycemia was unchanged.
Conclusions:
rhGH started early in the course of JIA preserved normal growth velocity and height. Although rhGH was well tolerated, carbohydrate metabolism should be monitored closely.
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