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首页> 外文期刊>Bone >Administration of romosozumab improves vertebral trabecular and cortical bone as assessed with quantitative computed tomography and finite element analysis
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Administration of romosozumab improves vertebral trabecular and cortical bone as assessed with quantitative computed tomography and finite element analysis

机译:通过定量计算机断层扫描和有限元分析评估,罗莫唑单抗的给药可改善椎骨小梁和皮质骨

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摘要

Romosozumab inhibits sclerostin, thereby increasing bone formation and decreasing bone resorption. This dual effect of romosozumab leads to rapid and substantial increases in areal bone mineral density (aBMD) as measured by dual-energy X-ray absorptiometry (DXA). In a phase 1b, randomized, double-blind, placebo-controlled study, romosozumab or placebo was administered to 32 women and 16 men with low aBMD for 3 months, with a further 3-month follow-up: women received six doses of 1 or 2 mg/kg every 2 weeks (Q2W) or three doses of 2 or 3 mg/kg every 4 weeks (Q4W); men received 1 mg/kg Q2W or 3 mg/kg Q4W. Quantitative computed tomography (QCT) scans at lumbar (L1-2) vertebrae and high-resolution QCT (HR-QCT) scans at thoracic vertebra (T12) were analyzed in a subset of subjects at baseline, month 3, and month 6. The QCT subset included 24 romosozumab and 9 placebo subjects and the HR-QCT subset included 11 romosozumab and 3 placebo subjects. The analyses pooled the romosozumab doses. Linear finite element modeling of bone stiffness was performed. Compared with placebo, the romosozumab group showed improvements at month 3 for trabecular BMD by QCT and HR-QCT, HR-QCT trabecular bone volume fraction (BV/TV) and separation,, density-weighted cortical thickness, and QCT stiffness (all p < 0.05). At month 6, improvements from baseline were observed in QCT trabecular BMD and stiffness, and. in HR-QCT BMD, trabecular BV/TV and separation, density-weighted cortical thickness, and stiffness in the romosozumab group (all p < 0.05 compared with placebo). The mean (SE) increase in HR-QCT stiffness with romosozumab from baseline was 26.9% +/- 6.8% and 35.0% +/- 6.8% at months 3 and 6, respectively; subjects administered placebo had changes of -2.7% +/- 13.4% and -6.4% +/- 13.4%, respectively. In conclusion, romosozumab administered for 3 months resulted in rapid and large improvements in trabecular and cortical bone mass and structure as well as whole bone stiffness, which continued 3 months after the last romosozumab,dose. (C) 2015 Published by Elsevier Inc.
机译:Romosozumab抑制硬化素,从而增加骨形成并减少骨吸收。如通过双能X射线吸收法(DXA)测量的那样,罗莫昔单抗的这种双重作用导致面骨矿物质密度(aBMD)的快速和大幅增加。在1b期随机,双盲,安慰剂对照研究中,将romosozumab或安慰剂施用于32名女性和16名aBMD低的男性,持续3个月,并进一步随访3个月:女性接受6剂1剂或每2周2毫克/公斤(Q2W)或每4周3剂量2或3毫克/公斤(Q4W);男性接受1 mg / kg Q2W或3 mg / kg Q4W。在基线,第3个月和第6个月的一组受试者中分析了腰椎(L1-2)椎骨的定量计算机断层扫描(QCT)扫描和胸椎骨(T12)的高分辨率QCT(HR-QCT)扫描。 QCT子集包括24个romosozumab和9个安慰剂受试者,HR-QCT子集包括11个romosozumab和3个安慰剂受试者。分析汇总了romosozumab剂量。进行骨刚度的线性有限元建模。与安慰剂相比,romosozumab组在第3个月的QCT和HR-QCT,HR-QCT小梁骨体积分数(BV / TV)和分离,密度加权皮质厚度和QCT刚度(所有p <0.05)。在第6个月,观察到QCT小梁BMD和刚度较基线有所改善。 HR-QCT的BMD,romosozumab组的骨小梁BV / TV和分离,密度加权皮质厚度和刚度(与安慰剂相比,所有p <0.05)。在第3个月和第6个月,romosozumab从基线开始的HR-QCT刚度平均增加(SE)分别为26.9%+/- 6.8%和35.0%+/- 6.8%;服用安慰剂的受试者的变化分别为-2.7%+/- 13.4%和-6.4%+/- 13.4%。总之,给予罗莫佐单抗治疗3个月后,小梁和皮质骨的质量和结构以及整个骨骼的硬度得到了快速而大的改善,在最后一次罗莫佐单抗给药后3个月持续进行。 (C)2015年由Elsevier Inc.出版

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