Kusumi Kirsten, Ayoob Rose, Bowden Sasigarn A, Ingraham Susan, Mahan John D
Division of Nephrology, Department of Pediatrics, Nationwide Children's Hospital/The Ohio State University, 700 Children's Dr., Columbus, OH, 43205, USA,
J Bone Miner Metab. 2015 Sep;33(5):560-8. doi: 10.1007/s00774-014-0618-2. Epub 2014 Oct 16.
Osteogenesis imperfecta (OI) is an inherited disorder characterized by bone fragility and low bone mass. Low bone density and fracture is a cause of morbidity. Limited data exists on bisphosphonate treatment in patients under 24 months of age. The objective of the study was to examine the safety and efficacy of pamidronate in children under 24 months with OI. To do so, we carried out a retrospective chart review and analysis of OI patients started on intravenous pamidronate under 24 months of age. Pamidronate was administered in three-day cycles. Growth, the number of fractures, and lumbar bone mineral densities were recorded both prior to and after treatment initiation. A total of 18 patients were reviewed. Five were classified as OI type I, seven were type III, and six were type IV. The mean age at treatment initiation was 12 months (range 11 days to 23 months). The mean lumbar z score at baseline was -3.63, which improved to -1.53 at one year (P < 0.01) and 0.79 (P < 0.01) at the end of the study. The fracture rate improved from 68 fractures in 209 months (0.32 fractures/patient-month) before treatment to 41 fractures in 1,248 months (0.03 fractures/patient-month) post-treatment (P < 0.05). Height standard deviation score (SDS) was conserved from baseline to end of study (-2.12 ± 2.45 vs. -2.45 ± 2.73) (P = 0.05) with an average follow-up of 73 months. The only adverse effect recorded in six infants was fever during the initial pamidronate infusion. Treatment with intravenous pamidronate is safe, significantly improves lumbar bone mineral density (L-BMD), and reduces fracture rates in young infants with OI while preserving linear growth.
成骨不全症(OI)是一种遗传性疾病,其特征为骨骼脆弱和骨量低。低骨密度和骨折是发病的原因。关于24个月以下患者使用双膦酸盐治疗的数据有限。本研究的目的是检验帕米膦酸对24个月以下成骨不全症患儿的安全性和有效性。为此,我们对24个月以下开始静脉注射帕米膦酸的成骨不全症患者进行了回顾性病历审查和分析。帕米膦酸以三天为一个周期给药。在开始治疗前和治疗后记录生长情况、骨折数量和腰椎骨矿物质密度。共审查了18例患者。5例为I型成骨不全症,7例为III型,6例为IV型。开始治疗时的平均年龄为12个月(范围为11天至23个月)。基线时腰椎z评分的平均值为-3.63,在1年时改善至-1.53(P<0.01),在研究结束时改善至0.79(P<0.01)。骨折率从治疗前209个月的68次骨折(0.32次骨折/患者-月)降至治疗后1248个月的41次骨折(0.03次骨折/患者-月)(P<0.05)。身高标准差评分(SDS)从基线到研究结束时保持不变(-2.12±2.45对-2.45±2.73)(P=0.05),平均随访73个月。在6名婴儿中记录到的唯一不良反应是初次输注帕米膦酸期间发热。静脉注射帕米膦酸治疗是安全的,可显著提高腰椎骨矿物质密度(L-BMD),降低成骨不全症幼儿的骨折率,同时保持线性生长。