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A randomized, controlled dose-ranging study of risedronate in children with moderate and severe osteogenesis imperfecta

Bishop, Nick; Harrison, Rachel; Ahmed, Faisal; Shaw, Nick; Eastell, Richard; Campbell, Mike; Knowles, Elizabeth; Hill, Claire; Hall, Christine; Chapman, Steve; Sprigg, Alan; Rigby, Alan

Authors

Nick Bishop

Rachel Harrison

Faisal Ahmed

Nick Shaw

Richard Eastell

Mike Campbell

Elizabeth Knowles

Claire Hill

Christine Hall

Steve Chapman

Alan Sprigg



Abstract

Moderate to severe osteogenesis imperfecta is associated with multiple fractures in childhood. There are no published data regarding the effects of third-generation bisphosphonates in these children. This randomized study investigated which of three different doses of risedronate was most effective in reducing fracture incidence. We randomly assigned 53 children with moderate to severe osteogenesis imperfecta to receive 0.2, 1, or 2 mg/kg per week of risedronate. We assessed safety, fracture incidence, and bone measurement outcomes at 3, 6, 12, 18, and 24 months. At 24 months, 69% of children assigned 0.2 mg/kg per week had had new fractures compared with 44% receiving 1 mg/kg per week and 75% receiving 2 mg/kg per week. Poisson regression with age and prior fracture as covariates showed that there was no difference in incident nonvertebral fracture between groups. Fracture rate diminished in each group during the trial compared with previous the 2 years (p = .005). Lumbar spine bone mineral density increased significantly (p = .009) only in the 2 mg/kg per week group. Long bone bowing deformities reduced more in children receiving 1 or 2 mg/kg per week of risedronate [odds ratio (OR) 0.67, 95% confidence interval (CI) 0.48-0.93 per unit increase in risedronate dose, p = .015]. There were no serious adverse events. Bone mass increased and bowing deformities reduced with increasing risedronate dose. Children suffered fewer fractures irrespective of risedronate dose. The most appropriate dose of risedronate for children with moderate to severe osteogenesis imperfecta in this study was 2 mg/kg per week. © 2010 American Society for Bone and Mineral Research.

Citation

Bishop, N., Harrison, R., Ahmed, F., Shaw, N., Eastell, R., Campbell, M., …Rigby, A. (2010). A randomized, controlled dose-ranging study of risedronate in children with moderate and severe osteogenesis imperfecta. Journal of Bone and Mineral Research, 25(1), 32-40. https://doi.org/10.1359/jbmr.090712

Journal Article Type Article
Acceptance Date Jul 1, 2009
Online Publication Date Dec 18, 2009
Publication Date 2010-01
Deposit Date Nov 13, 2014
Journal Journal Of Bone And Mineral Research
Print ISSN 0884-0431
Electronic ISSN 1523-4681
Publisher American Society for Bone and Mineral Research
Peer Reviewed Peer Reviewed
Volume 25
Issue 1
Pages 32-40
DOI https://doi.org/10.1359/jbmr.090712
Keywords Endocrinology, Diabetes and Metabolism; Orthopedics and Sports Medicine
Public URL https://hull-repository.worktribe.com/output/472883