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首页> 外文期刊>JBMR plus. >Administration of Denosumab Preserves Bone Mineral Density at the Knee in Persons With Subacute Spinal Cord Injury: Findings From a Randomized Clinical Trial
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Administration of Denosumab Preserves Bone Mineral Density at the Knee in Persons With Subacute Spinal Cord Injury: Findings From a Randomized Clinical Trial

机译:Deaosumab的施用在亚克斯脊髓损伤的人的膝盖上保留了骨矿物密度:来自随机临床试验的研究结果

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Persons with neurologically motor‐complete spinal cord injury (SCI) have a marked loss of bone mineral density (BMD) of the long bones of the lower extremities, predisposing them to fragility fractures, especially at the knee. Denosumab, a commercially available human monoclonal IgG antibody to receptor activator of nuclear factor‐κB ligand (RANKL), may provide an immunopharmacological solution to the rapid progressive deterioration of sublesional bone after SCI. Twenty‐six SCI participants with subacute motor‐complete SCI were randomized to receive either denosumab (60?mg) or placebo at baseline (BL), 6, and 12?months. Areal bone mineral density (aBMD) by dual energy x‐ray absorptiometry (DXA) at 18?months at the distal femur was the primary outcome and aBMD of the proximal tibia and hip were the secondary outcomes analyzed in 18 of the 26 participants (denosumab, n = 10 and placebo, n = 8). The metrics of peripheral QCT (pQCT) were the exploratory outcomes analyzed in a subsample of the cohort (denosumab, n = 7 and placebo n = 7). The mean aBMD (±95% CI) for the denosumab versus the placebo groups demonstrated a significant group × time interactions for the following regions of interest at BL and 18?months: distal femoral metaphysis = mean aBMD 1.187; 95% CI, 1.074 to 1.300 and mean aBMD 1.202; 95% CI, 1.074 to 1.329 versus mean aBMD 1.162; 95% CI, 0.962 to 1.362 and mean aBMD 0.961; 95% CI, 0.763 to 1.159, respectively ( p ?0.001); distal femoral epiphysis = mean aBMD 1.557; 95% CI, 1.437 to 1.675 and mean aBMD 1.570; 95% CI, 1.440 to 1.700 versus mean aBMD 1.565; 95% CI, 1.434 to 1.696 and mean aBMD 1.103; 95% CI, 0.898 to 1.309, respectively ( p = 0.002); and proximal tibial epiphysis = mean aBMD 1.071; 95% CI, 0.957 to 1.186 and mean aBMD 1.050; 95% CI, 0.932 to 1.168 versus mean aBMD 0.994; 95% CI, 0.879 to 1.109 and mean aBMD 0.760; 95% CI, 0.601 to 0.919, respectively ( p ?0.001). Analysis of pQCT imaging revealed a continued trend toward significantly greater loss in total volumetric BMD (vBMD) and trabecular vBMD at the 4% distal tibia region, with a significant percent loss for total bone mineral content. Thus, at 18?months after acute SCI, our findings show that denosumab maintained aBMD at the knee region, the site of greatest clinical relevance in the SCI population. ? 2020 The Authors. JBMR Plus published by Wiley Periodicals LLC. on behalf of American Society for Bone and Mineral Research.
机译:具有神经主动动电动机完全脊髓损伤(SCI)的人具有下肢长骨的骨矿物密度(BMD)的显着损失,使它们易于脆弱的骨折,特别是在膝盖上。 Denosumab是核因子-κB配体(RANKL)的可商购的人单克隆IgG抗体,可为SCI后悬浮骨的快速渐进性劣化提供免疫医药溶液。二十六次与亚急性电动机完全SCI的SCI参与者随机分配,以在基线(BL),6和12个月内接收Denosumab(60?Mg)或安慰剂。通过双能X射线吸收度(DXA)在远端股骨的18℃的区域骨矿物密度(DXA)是近端胫骨和髋关节的主要结果,是26名参与者中18名(DeNosumab)中分析的二次结果,n = 10和安慰剂,n = 8)。外周QCT(PQCT)的度量是在队列的子样本中分析的探索性结果(DeNOSumab,N = 7和安慰剂N = 7)。 DenoSumab与安慰剂组的平均ABMD(±95%CI)表现出对BL和18个月的以下感兴趣区域的显着组×时间相互作用?数月:远端股骨质Metaphyse =平均ABMD 1.187; 95%CI,1.074至1.300,平均ABMD 1.202; 95%CI,1.074至1.329与平均ABMD 1.162; 95%CI,0.962至1.362,平均abmd 0.961; 95%CI,分别为0.763至1.159(P <0.001);远端股骨骨骺=平均ABMD 1.557; 95%CI,1.437至1.675,平均值1.570; 95%CI,1.440至1.700与平均ABMD 1.565; 95%CI,1.434至1.696,平均为ABMD 1.103; 95%CI,分别为0.898至1.309(p = 0.002);和近端胫骨骨骺=平均ABMD 1.071; 95%CI,0.957至1.186,平均ABMD 1.050; 95%CI,0.932至1.168与平均abmd 0.994; 95%CI,0.879至1.109,平均值为ABMD 0.760; 95%CI,分别为0.601至0.919(P <0.001)。 PQCT成像分析显示,在4%远端胫骨区域的总体积BMD(VBMD)和小梁VBMD中持续趋势持续趋势,具有显着的骨矿物质含量损失较高。因此,在急性SCI后18个月,我们的研究结果表明,Denosumab在SCI人群中最大的临床相关性的临床意义的遗址维持了ABMD。 ? 2020作者。 JBMR Plus由Wiley期刊LLC发布。代表美国人骨骼和矿物学研究。

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