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罗莫单抗与特立帕肽相比对低骨量绝经后女性脊柱和髋部骨密度及骨量的影响。

Effects of Romosozumab Compared With Teriparatide on Bone Density and Mass at the Spine and Hip in Postmenopausal Women With Low Bone Mass.

作者信息

Genant Harry K, Engelke Klaus, Bolognese Michael A, Mautalen Carlos, Brown Jacques P, Recknor Chris, Goemaere Stefan, Fuerst Thomas, Yang Yu-Ching, Grauer Andreas, Libanati Cesar

机构信息

University of California, San Francisco (UCSF), San Francisco, CA, USA.

BioClinica-Synarc, San Francisco, CA, USA.

出版信息

J Bone Miner Res. 2017 Jan;32(1):181-187. doi: 10.1002/jbmr.2932. Epub 2016 Sep 20.

Abstract

Romosozumab, a monoclonal antibody that binds sclerostin, has a dual effect on bone by increasing bone formation and reducing bone resorption, and thus has favorable effects in both aspects of bone volume regulation. In a phase 2 study, romosozumab increased areal BMD at the lumbar spine and total hip as measured by DXA compared with placebo, alendronate, and teriparatide in postmenopausal women with low bone mass. In additional analyses from this international, randomized study, we now describe the effect of romosozumab on lumbar spine and hip volumetric BMD (vBMD) and BMC at month 12 as assessed by QCT in the subset of participants receiving placebo, s.c. teriparatide (20 µg once daily), and s.c. romosozumab (210 mg once monthly). QCT measurements were performed at the lumbar spine (mean of L and L entire vertebral bodies, excluding posterior processes) and hip. One year of treatment with romosozumab significantly increased integral vBMD and BMC at the lumbar spine and total hip from baseline, and compared with placebo and teriparatide (all p < 0.05). Trabecular vertebral vBMD improved significantly and similarly from baseline (p < 0.05) with both romosozumab (18.3%) and teriparatide (20.1%), whereas cortical vertebral vBMD gains were larger with romosozumab compared with teriparatide (13.7% versus 5.7%, p < 0.0001). Trabecular hip vBMD gains were significantly larger with romosozumab than with teriparatide (10.8% versus 4.2%, p = 0.01), but were similar for cortical vBMD (1.1% versus -0.9%, p = 0.12). Cortical BMC gains were larger with romosozumab compared with teriparatide at both the spine (23.3% versus 10.9%, p < 0.0001) and hip (3.4% versus 0.0%, p = 0.03). These improvements are expected to result in strength gains and support the continued clinical investigation of romosozumab as a potential therapy to rapidly reduce fracture risk in ongoing phase 3 studies. © 2016 American Society for Bone and Mineral Research.

摘要

罗莫单抗是一种可结合硬化蛋白的单克隆抗体,它通过增加骨形成和减少骨吸收对骨骼产生双重作用,因此在骨量调节的两个方面均具有有益效果。在一项2期研究中,与安慰剂、阿仑膦酸盐和特立帕肽相比,罗莫单抗使低骨量绝经后女性通过双能X线吸收法(DXA)测得的腰椎和全髋部面积骨密度增加。在这项国际随机研究的其他分析中,我们现在描述了在接受安慰剂、皮下注射特立帕肽(每日一次,20μg)和皮下注射罗莫单抗(每月一次,210mg)的参与者亚组中,通过定量计算机断层扫描(QCT)评估罗莫单抗在第12个月时对腰椎和髋部体积骨密度(vBMD)及骨矿含量(BMC)的影响。QCT测量在腰椎(L1和L2整个椎体的平均值,不包括椎弓根)和髋部进行。罗莫单抗治疗一年后,腰椎和全髋部的整体vBMD和BMC较基线水平显著增加,且与安慰剂和特立帕肽相比均有统计学差异(所有p<0.05)。罗莫单抗(18.3%)和特立帕肽(20.1%)治疗后,椎骨小梁vBMD较基线水平均有显著且相似的改善(p<0.05),而罗莫单抗治疗后皮质骨vBMD的增加幅度大于特立帕肽(13.7%对5.7%,p<0.0001)。罗莫单抗治疗后髋部小梁骨vBMD的增加幅度显著大于特立帕肽(10.8%对4.2%,p=0.01),但皮质骨vBMD的增加幅度相似(1.1%对-0.9%,p=0.12)。罗莫单抗治疗后,脊柱和髋部的皮质骨BMC增加幅度均大于特立帕肽(脊柱:23.3%对10.9%,p<0.0001;髋部:3.4%对0.0%,p=0.03)。这些改善预期会带来强度增加,并支持罗莫单抗作为一种潜在疗法在正在进行的3期研究中继续进行临床研究,以快速降低骨折风险。©2016美国骨与矿物质研究学会

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