Department of Rheumatology, Charles Nicolle Hospital, Tunis.
University of Tunis El Manar.
J Pediatr Orthop B. 2024 May 1;33(3):283-289. doi: 10.1097/BPB.0000000000001104. Epub 2023 Jun 20.
Osteogenesis imperfecta is an inherited clinically heterogeneous disorder of bone metabolism characterized by bone and skeletal fragility and an increased risk of fractures. Pamidronate infusion was the standard treatment, but zoledronic acid is increasingly used to treat children with osteogenesis imperfecta. We conducted a systematic literature review to evaluate the efficacy and safety of intravenous zoledronic acid in the treatment of osteogenesis imperfecta in pediatric patients. A systematic review of the published literature was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Eligible articles were clinical trials and observational studies including pediatric patients (<16 years) with osteogenesis imperfecta treated with zoledronic acid. We selected articles published during the 20 past years. The selected languages were English and French. We included articles with a minimum sample size of five patients. Six articles fulfilled the selection criteria. The majority of patients were Chinese (58%). The predominant sex was male (65%), and the age of included patients ranged from 2.5 weeks to 16.8 years. For all patients, zoledronic infusions were administrated intravenously. The zoledronic treatment duration ranged from 1 to 3 years. Densitometry parameters before and after zoledronic treatment were evaluated and showed significant improvement both in lumbar spine-bone mineral density Z -score and femoral neck-bone mineral density Z -scores. A significant decrease in fracture rate has also been noted both in vertebral and nonvertebral fracture incidence. The two most common side effects were fever and flu-like reactions. None of the patients presented severe adverse events. Zoledronic acid appeared to be well-tolerated and effective in the treatment of pediatric osteogenesis imperfecta.
成骨不全症是一种遗传性的、临床表现异质性的骨骼代谢疾病,其特征为骨骼脆弱,骨折风险增加。帕米膦酸盐输注是标准治疗方法,但唑来膦酸越来越多地用于治疗成骨不全症患儿。我们进行了一项系统文献综述,以评估静脉用唑来膦酸治疗儿童成骨不全症的疗效和安全性。根据系统评价和荟萃分析的首选报告项目指南,对已发表的文献进行了系统综述。合格的文章是临床试验和观察性研究,包括用唑来膦酸治疗的成骨不全症儿科患者(<16 岁)。我们选择了过去 20 年发表的文章。所选语言为英语和法语。我们纳入了最小样本量为 5 例患者的文章。有 6 篇文章符合选择标准。大多数患者为中国人(58%)。主要性别为男性(65%),纳入患者的年龄范围为 2.5 周至 16.8 岁。所有患者均接受唑来膦酸静脉输注。唑来膦酸治疗时间从 1 年到 3 年不等。评估了唑来膦酸治疗前后的骨密度参数,发现腰椎骨密度 Z 评分和股骨颈骨密度 Z 评分均有显著改善。椎体和非椎体骨折发生率也显著降低。最常见的两种副作用是发热和流感样反应。无患者出现严重不良事件。唑来膦酸治疗儿童成骨不全症似乎耐受良好且有效。