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[Long-term steroid therapy in children: is adjunct therapy relevant in nephrotic syndrome?]
J Bacchetta1, J Harambat, P Cochat
1Service de néphrologie et rhumatologie pédiatriques, centre de référence des maladies rénales rares, hôpital Femme-Mère-Enfant, université de Lyon, 69677 Bron, France.
Insights
Glucocorticoids harm bone development in children. Routine vitamin D and calcium, alongside lifestyle changes, may help prevent bone disease in children undergoing long-term steroid treatment.
Area of Science:
- Pediatric Endocrinology
- Bone Metabolism
- Pharmacology
Background:
- Glucocorticoids negatively impact bone formation by inhibiting osteoblasts.
- Long-term corticosteroid use in children can cause delayed bone maturation, hypogonadism, and reduced Insulin-like Growth Factor 1 (IGF1).
Purpose of the Study:
- To systematically review interventions for preventing bone disease in children receiving long-term steroid therapy.
Main Methods:
- A systematic review of 12 clinical trials was conducted.
- Interventions included calcium, vitamin D, growth hormone, calcitonin, and bisphosphonates.
- Limited number of randomized controlled trials (n=7) precluded meta-analysis.
Main Results:
- Calcium and vitamin D supplementation showed potential benefits for bone health in children with nephrotic syndrome on long-term steroids.
- Few high-quality randomized controlled trials were identified.
Conclusions:
- Routine vitamin D supplementation is recommended for children on long-term steroid therapy.
- Steroid-sparing protocols and comprehensive bone protection strategies (calcium, sun exposure, physical activity) are advised.
Abstract:
The impact of glucocorticoids on bone is specifically relevant in children exposed to a long course of treatment. Corticosteroids lead to a decrease in bone formation, mainly by osteoblastic inhibition in trabecular bone. They also play an indirect role in bone metabolism through systemic actions, such as bone maturation delay, hypogonadism, pubertal delay, and IGF1 inhibition. A systematic review of the literature was conducted. We found 12 clinical trials of interventions including calcium, vitamin D, growth hormone, calcitonin, and bisphosphonates for preventing bone disease in children receiving steroid therapy. There were few randomized controlled trials (n=7), with a limited number of patients, so that a meta-analysis could not be performed. Calcium and vitamin D supplementation may, however, have a beneficial effect on bone in children with nephrotic syndrome receiving long-term steroid therapy. We, therefore, recommend routine vitamin D supplementation, use of steroid-sparing protocols, and global prevention of risk to bone (adequate calcium intake, sun exposure, and physical activity).
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