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Comparison of proximal femur and vertebral body strength improvements in the FREEDOM trial using an alternative finite element methodology

机译:使用替代有限元方法在FREEDOM试验中比较股骨近端和椎体强度的改善

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Denosumab reduced the incidence of new fractures in postmenopausal women with osteoporosis by 68% at the spine and 40% at the hip over 36 months compared with placebo in the FREEDOM study. This efficacy was supported by improvements from baseline in vertebral (18.2%) strength in axial compression and femoral (8.6%) strength in sideways fall configuration at 36 months, estimated in Newtons by an established voxel-based finite element (FE) methodology. Since FE analyses rely on the choice of meshes, material properties, and boundary conditions, the aim of this study was to independently confirm and compare the effects of denosumab on vertebral and femoral strength during the FREEDOM trial using an alternative smooth FE methodology. Unlike the previous FE study, effects on femoral strength in physiological stance configuration were also examined. QCT data for the proximal femur and two lumbar vertebrae were analyzed by smooth FE methodology at baseline, 12, 24, and 36 months for 51 treated (denosumab) and 47 control (placebo) subjects. QCT images were segmented and converted into smooth FE models to compute bone strength. L1 and L2 vertebral bodies were virtually loaded in axial compression and the proximal femora in both fall and stance configurations. Denosumab increased vertebral body strength by 10.8%, 14.0%, and 17.4% from baseline at 12, 24, and 36 months, respectively (p < 0.0001). Denosumab also increased femoral strength in the fall configuration by 4.3%, 5.1%, and 7.2% from baseline at 12, 24, and 36 months, respectively (p < 0.0001). Similar improvements were observed in the stance configuration with increases of 4.2%, 5.2%, and 5.2% from baseline (p <= 0.0007). Differences between the increasing strengths with denosumab and the decreasing strengths with placebo were significant starting at 12 months (vertebral and femoral fall) or 24 months (femoral stance). Using an alternative smooth FE methodology, we confirmed the significant improvements in vertebral body and proximal femur strength previously observed with denosumab. Estimated increases in strength with denosumab and decreases with placebo were highly consistent between both FE techniques. (C) 2015 Elsevier Inc. All rights reserved.
机译:与FREEDOM研究中的安慰剂相比,在36个月内,Denosumab将患有骨质疏松症的绝经后妇女的新骨折发生率降低了68%,脊柱骨和髋部40%。通过建立的基于体素的有限元(FE)方法在牛顿中评估,在36个月时,椎体轴向受压的基线强度(18.2%)和股骨(8.6%)强度的基线得到改善,从而支持了该功效。由于有限元分析依赖于网格,材料特性和边界条件的选择,因此本研究的目的是使用替代的光滑有限元方法在FREEDOM试验中独立确认和比较denosumab对椎骨和股骨强度的影响。与先前的有限元研究不同,还研究了在生理姿势配置中对股骨强度的影响。对于51位接受治疗的患者(denosumab)和47位对照(安慰剂)的受试者,在基线,12、24和36个月时采用平滑FE方法分析了股骨近端和两个腰椎的QCT数据。将QCT图像分割并转换为平滑的FE模型以计算骨骼强度。 L1和L2椎体在轴向受压时实际上处于负重状态,而股骨近端处于跌倒状态和站立状态。在12、24和36个月时,Denosumab分别使椎体强度比基线提高了10.8%,14.0%和17.4%(p <0.0001)。在跌倒状态下,Denosumab还在12、24和36个月时分别比基线提高了股骨强度4.3%,5.1%和7.2%(p <0.0001)。在姿势配置中观察到类似的改善,与基线相比分别增加了4.2%,5.2%和5.2%(p <= 0.0007)。地诺单抗的增加强度与安慰剂的减少强度之间的差异在12个月(椎体和股骨跌落)或24个月(股骨姿)开始时显着。使用另一种平滑的有限元方法,我们确认了以前用denosumab观察到的椎体和近端股骨强度的显着改善。两种FE技术之间,地诺单抗的强度增加估计值和安慰剂的强度下降高度一致。 (C)2015 Elsevier Inc.保留所有权利。

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