Trejo Pamela, Fassier François, Glorieux Francis H, Rauch Frank
Shriners Hospital for Children and McGill University, Montreal, Quebec, Canada.
J Bone Miner Res. 2017 May;32(5):1034-1039. doi: 10.1002/jbmr.3071. Epub 2017 Feb 28.
Several recent case reports have suggested that bisphosphonate treatment in individuals with osteogenesis imperfecta (OI) is causally related to atypical femur fractures. However, it is not known whether atypical femur fractures are actually more frequent in patients who have received bisphosphonates. In the present study, we retrospectively analyzed 166 femur fractures in 119 children with a diagnosis of OI that had not undergone intramedullary rodding procedures. A total of 130 fractures in 90 patients occurred in femurs with preexisting deformities (age at fracture between 1 month and 19.9 years; 43 girls). Because deformities are a typical cause of fracture in OI, deformed femurs were excluded from the analysis of atypical fractures. However, it was noted that in deformed femurs a transverse fracture pattern (one of the criteria of atypical fractures) was associated with a moderate to severe OI phenotype and not related to bisphosphonate treatment. Of the 36 fractures that occurred in nondeformed femurs (30 individuals; age at fracture between 1 month and 17.4 years; 13 girls), 11 (in nine children) occurred during bisphosphonate treatment. Three of these fractures (27%) resembled atypical femur fractures. Among the 25 femur fractures (23 patients) that occurred in the absence of prior bisphosphonate treatment, 8 (22%) resembled atypical femur fractures. Logistic regression analysis showed that bisphosphonate treatment history was not associated with the occurrence of atypical fractures. In contrast, the presence of moderate to severe OI (defined as any OI type other than OI type I) was strongly associated with atypical femur fractures. Thus, we observed an atypical appearance in about a quarter of nondeformed femur fractures that occurred in children with OI. Such atypical femur fractures seemed to be related to the severity of OI rather than to bisphosphonate treatment history. © 2016 American Society for Bone and Mineral Research.
最近的几例病例报告表明,成骨不全症(OI)患者接受双膦酸盐治疗与非典型股骨骨折存在因果关系。然而,接受双膦酸盐治疗的患者中,非典型股骨骨折的实际发生率是否更高尚不清楚。在本研究中,我们回顾性分析了119例诊断为OI且未接受髓内棒插入手术的儿童的166例股骨骨折情况。90例患者共发生130例骨折,骨折部位的股骨存在既往畸形(骨折时年龄在1个月至19.9岁之间;43例女孩)。由于畸形是OI患者骨折的典型原因,因此在非典型骨折分析中排除了畸形股骨。然而,值得注意的是,在畸形股骨中,横行骨折模式(非典型骨折的标准之一)与中度至重度OI表型相关,与双膦酸盐治疗无关。在36例非畸形股骨骨折中(30例个体;骨折时年龄在1个月至17.4岁之间;13例女孩),11例(9例儿童)发生在双膦酸盐治疗期间。其中3例骨折(27%)类似非典型股骨骨折。在25例未接受双膦酸盐治疗前发生的股骨骨折(23例患者)中,8例(22%)类似非典型股骨骨折。逻辑回归分析表明,双膦酸盐治疗史与非典型骨折的发生无关。相反,中度至重度OI(定义为除I型OI以外的任何OI类型)的存在与非典型股骨骨折密切相关。因此,我们观察到OI儿童非畸形股骨骨折中约四分之一呈现非典型外观。这种非典型股骨骨折似乎与OI的严重程度有关,而非双膦酸盐治疗史。© 2016美国骨与矿物质研究学会