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特立帕肽序贯地诺单抗治疗绝经前特发性骨质疏松症:通过高分辨率外周定量CT评估骨微结构和强度

Teriparatide Followed by Denosumab in Premenopausal Idiopathic Osteoporosis: Bone Microstructure and Strength by HR-pQCT.

作者信息

Agarwal Sanchita, Shiau Stephanie, Kamanda-Kosseh Mafo, Bucovsky Mariana, Kil Nayoung, Lappe Joan M, Stubby Julie, Recker Robert R, Guo X Edward, Shane Elizabeth, Cohen Adi

机构信息

Department of Medicine, Columbia University Vagelos College of Physicians & Surgeons, New York, NY, USA.

Department of Biostatistics & Epidemiology, Rutgers School of Public Health, Piscataway, NY, USA.

出版信息

J Bone Miner Res. 2023 Jan;38(1):35-47. doi: 10.1002/jbmr.4739. Epub 2022 Nov 24.

Abstract

Premenopausal women with idiopathic osteoporosis (PreMenIOP) have marked deficits in skeletal microstructure. We have reported that sequential treatment with teriparatide and denosumab improves central skeletal bone mineral density (BMD) by dual-energy X-ray absorptiometry and central QCT in PreMenIOP. We conducted preplanned analyses of high-resolution peripheral quantitative computed tomography (HR-pQCT) scans from teriparatide and denosumab extension studies to measure effects on volumetric BMD (vBMD), microarchitecture, and estimated strength at the distal radius and tibia. Of 41 women enrolled in the parent teriparatide study (20 mcg daily), 34 enrolled in the HR-pQCT study. HR-pQCT participants initially received teriparatide (N = 24) or placebo (N = 10) for 6 months; all then received teriparatide for 24 months. After teriparatide, 26 enrolled in the phase 2B denosumab extension (60 mg q6M) for 24 months. Primary outcomes were percentage change in vBMD, microstructure, and stiffness after teriparatide and after denosumab. Changes after sequential teriparatide and denosumab were secondary outcomes. After teriparatide, significant improvements were seen in tibial trabecular number (3.3%, p = 0.01), cortical area and thickness (both 2.7%, p < 0.001), and radial trabecular microarchitecture (number: 6.8%, thickness: 2.2%, separation: -5.1%, all p < 0.02). Despite increases in cortical porosity and decreases in cortical density, whole-bone stiffness and failure load increased at both sites. After denosumab, increases in total (3.5%, p < 0.001 and 3.3%, p = 0.02) and cortical vBMD (1.7% and 3.2%; both p < 0.01), and failure load (1.1% and 3.6%; both p < 0.05) were seen at tibia and radius, respectively. Trabecular density (3.5%, p < 0.001) and number (2.4%, p = 0.03) increased at the tibia, while thickness (3.0%, p = 0.02) increased at the radius. After 48 months of sequential treatment, significant increases in total vBMD (tibia: p < 0.001; radius: p = 0.01), trabecular microstructure (p < 0.05), cortical thickness (tibia: p < 0.001; radius: p = 0.02), and whole bone strength (p < 0.02) were seen at both sites. Significant increases in total vBMD and bone strength parameters after sequential treatment with teriparatide followed by denosumab support the use of this regimen in PreMenIOP. © 2022 American Society for Bone and Mineral Research (ASBMR).

摘要

患有特发性骨质疏松症的绝经前女性(PreMenIOP)在骨骼微结构方面存在明显缺陷。我们曾报道,特立帕肽和地诺单抗序贯治疗可通过双能X线吸收法和容积CT改善PreMenIOP患者的脊柱骨密度(BMD)。我们对来自特立帕肽和地诺单抗扩展研究的高分辨率外周定量计算机断层扫描(HR-pQCT)进行了预先计划的分析,以测量对桡骨远端和胫骨的骨体积密度(vBMD)、微结构及估计强度的影响。在最初参与特立帕肽研究(每日20μg)的41名女性中,有34名参与了HR-pQCT研究。HR-pQCT参与者最初接受特立帕肽(N = 24)或安慰剂(N = 10)治疗6个月;之后全部接受特立帕肽治疗24个月。特立帕肽治疗后,26名参与者进入2B期地诺单抗扩展研究(每6个月60mg),为期24个月。主要结局指标为特立帕肽治疗后及地诺单抗治疗后的vBMD、微结构及刚度的百分比变化。特立帕肽和地诺单抗序贯治疗后的变化为次要结局指标。特立帕肽治疗后,胫骨小梁数量显著增加(3.3%,p = 0.01),皮质面积和厚度均增加(均为2.7%,p < 0.001),桡骨小梁微结构也有改善(数量:6.8%,厚度:2.2%,间距:-5.1%,均p < 0.02)。尽管皮质孔隙率增加且皮质密度降低,但两个部位的全骨刚度和破坏载荷均增加。地诺单抗治疗后,胫骨和桡骨的总vBMD(分别为3.5%,p < 0.001和3.3%,p = 0.02)和皮质vBMD(分别为1.7%和3.2%;均p < 0.01)以及破坏载荷(分别为1.1%和3.6%;均p < 0.05)均增加。胫骨的小梁密度(3.5%,p < 0.001)和数量(2.4%,p = 0.03)增加,桡骨的小梁厚度(3.0%,p = 0.02)增加。序贯治疗48个月后,两个部位的总vBMD(胫骨:p < 0.001;桡骨:p = 0.01)、小梁微结构(p < 0.05)、皮质厚度(胫骨:p < 0.001;桡骨:p = 0.02)和全骨强度(p < 0.02)均显著增加。特立帕肽后序贯地诺单抗治疗后总vBMD和骨强度参数显著增加,支持该方案在PreMenIOP中的应用。© 2022美国骨与矿物研究学会(ASBMR)

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