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

被引:14
作者
Agarwal, Sanchita [1 ,5 ]
Shiau, Stephanie [2 ]
Kamanda-Kosseh, Mafo [1 ]
Bucovsky, Mariana [1 ]
Kil, Nayoung [1 ]
Lappe, Joan M. M. [3 ]
Stubby, Julie [3 ]
Recker, Robert R. R. [3 ]
Guo, X. Edward [4 ]
Shane, Elizabeth [1 ]
Cohen, Adi [1 ]
机构
[1] Columbia Univ, Dept Med, Vagelos Coll Phys & Surg, New York, NY 10032 USA
[2] Rutgers Sch Publ Hlth, Dept Biostat & Epidemiol, Piscataway, NY USA
[3] Creighton Univ, Dept Med, Med Ctr, Omaha, NE USA
[4] Columbia Univ, Dept Biomed Engn, Bone Bioengn Lab, New York, NY 10032 USA
[5] Columbia Univ, Vagelos Coll Phys & Surg, Dept Med, Div Endocrinol, 180 Ft Washington Ave, HP9-910, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
PREMENOPAUSAL OSTEOPOROSIS; TERIPARATIDE; DENOSUMAB; BONE MICROSTRUCTURE; BONE STRENGTH; QUANTITATIVE COMPUTED-TOMOGRAPHY; (ITS)-BASED MORPHOLOGICAL ANALYSIS; DISTAL RADIUS; POSTMENOPAUSAL WOMEN; TRABECULAR BONE; CORTICAL BONE; ELEMENT-ANALYSIS; MECHANICAL-PROPERTIES; FAILURE LOAD; ILIAC CREST;
D O I
10.1002/jbmr.4739
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. (C) 2022 American Society for Bone and Mineral Research (ASBMR).
引用
收藏
页码:35 / 47
页数:13
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