Thornton J, Ashcroft D M, Mughal M Z, Elliott R A, O'Neill T W, Symmons D
Arthritis Research Campaign Epidemiology Unit, Division of Epidemiology and Health Sciences, University of Manchester, UK.
Arch Dis Child. 2006 Sep;91(9):753-61. doi: 10.1136/adc.2006.093997. Epub 2006 May 11.
To evaluate the currently available evidence for the effectiveness of bisphosphonates in children with low bone mineral density (BMD) and fragility fractures associated with juvenile idiopathic arthritis (JIA), and the safety of bisphosphonates in JIA and other conditions.
Literature databases were searched using a structured search strategy. The effectiveness review included any studies of children with JIA treated with bisphosphonates. The safety review also included studies of osteogenesis imperfecta. Quantitative data analysis was not undertaken because of the heterogeneity of the studies; findings were summarised using tables and narrative synthesis.
Ninety four studies were identified. Sixteen studies (78 JIA children) were included in the effectiveness review: one randomised controlled trial, three controlled cohort studies, 11 case series, and one case report. At baseline, children had low BMD below the expected values for age and sex matched children. In all studies, treatment with bisphosphonates increased BMD compared with baseline: the mean percentage increase in spine BMD ranged from 4.5% to 19.1%. Overall, studies were heterogeneous and of variable quality. A total of 59 papers were included in the safety review; treatment durations were up to three years. The most common side effect was a flu-like reaction with intravenous treatment. This occurred during the first infusion and was transient; the symptoms were managed with paracetamol and did not occur during subsequent cycles.
Bisphosphonates are a promising treatment for low BMD and fragility fractures in children with JIA. However, the quality of the current evidence is variable and better studies are needed to more clearly assess their role.
评估目前关于双膦酸盐对患有低骨矿物质密度(BMD)以及与幼年特发性关节炎(JIA)相关的脆性骨折的儿童的有效性,以及双膦酸盐在JIA和其他病症中的安全性的现有证据。
使用结构化检索策略对文献数据库进行检索。有效性综述纳入了所有用双膦酸盐治疗JIA儿童的研究。安全性综述还纳入了成骨不全症的研究。由于研究的异质性,未进行定量数据分析;研究结果通过表格和叙述性综合进行总结。
共识别出94项研究。有效性综述纳入了16项研究(78名JIA儿童):1项随机对照试验、3项对照队列研究、11项病例系列研究和1项病例报告。在基线时,儿童的BMD低于年龄和性别匹配儿童预期值。在所有研究中,与基线相比,双膦酸盐治疗可提高BMD:脊柱BMD的平均百分比增幅在4.5%至19.1%之间。总体而言,研究具有异质性且质量参差不齐。安全性综述共纳入59篇论文;治疗持续时间最长为三年。最常见的副作用是静脉治疗时出现类似流感的反应。这发生在首次输注期间,且为一过性;症状用对乙酰氨基酚处理,后续周期未再出现。
双膦酸盐对于JIA儿童的低BMD和脆性骨折是一种有前景的治疗方法。然而,当前证据的质量参差不齐,需要更好的研究来更清楚地评估它们的作用。