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Safety of growth hormone treatment in children with juvenile idiopathic arthritis
1Department of Endocrinology and Diabetology, Hôpital Robert Debré, FR-75019 Paris, France. dominique.simon@rdb.aphp.fr
Insights
Growth hormone (GH) therapy in children with juvenile idiopathic arthritis (JIA) on glucocorticoids shows a good safety profile. Cautious consideration is advised due to limited patient numbers and follow-up duration.
Area of Science:
- Pediatric Endocrinology
- Rheumatology
- Pharmacology
Background:
- Children with juvenile idiopathic arthritis (JIA) often require glucocorticoid therapy.
- Growth hormone (GH) therapy is considered for growth deficits in these patients.
- Concerns exist regarding the combined use of GH and glucocorticoids.
Purpose of the Study:
- To review available data on the safety of GH therapy in children with JIA receiving glucocorticoids.
- To provide recommendations for monitoring patients undergoing combined therapy.
Main Methods:
- Review of published data on GH therapy in glucocorticoid-treated children with JIA.
- Analysis of reported adverse events, including effects on joint disease and glucose tolerance.
Main Results:
- GH therapy in this population demonstrates a satisfactory safety profile.
- Adverse effects on the joint disease course are rarely reported.
- Impaired glucose tolerance has been uncommon in clinical trials.
Conclusions:
- GH therapy appears safe for children with JIA on glucocorticoids.
- Initiation of GH therapy warrants cautious decision-making due to limited patient data and follow-up durations.
Background:
Available data on growth hormone (GH) therapy in glucocorticoid-treated children with juvenile idiopathic arthritis (JIA) suggest a satisfactory safety profile. There have been few reports of adverse effects on the course of the joint disease (e.g., inflammatory flare-ups or osteoarticular complications). Despite strong concern that combined glucocorticoid and GH therapy might impair glucose tolerance, this has been uncommon in clinical trials. This article briefly reviews the published data and offers recommendations for monitoring patients with JIA who are receiving GH replacement therapy.
Conclusions:
The safety of GH therapy in children receiving glucocorticoid therapy for JIA seems satisfactory with few serious adverse events reported to date; however, given the small number of treated patients and the short periods of follow-up in each individual patient, the decision to initiate GH therapy in patients receiving glucocorticoids should be made cautiously.
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