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首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Quantitative computed tomographic assessment of the effects of 24 months of teriparatide treatment on 3D femoral neck bone distribution, geometry, and bone strength: results from the EUROFORS study.
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Quantitative computed tomographic assessment of the effects of 24 months of teriparatide treatment on 3D femoral neck bone distribution, geometry, and bone strength: results from the EUROFORS study.

机译:定量计算机断层扫描评估24个月teriparatide治疗对3D股骨颈骨分布,几何形状和骨强度的影响:EUROFORS研究的结果。

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摘要

We studied the changes in bone distribution, geometry, and bone strength based on 3D quantitative computed tomography (QCT) of the femoral neck (FN) in subjects receiving teriparatide (TPTD). Fifty-two postmenopausal women with severe osteoporosis were analyzed. Patients were divided into three subgroups based on their prior treatment with osteoporosis drugs: treatment-naive (Tx-naive; n = 8), pretreated (pre-Tx; n = 12), and pretreated showing an inadequate response to treatment (inad. pre-Tx; n = 32). QCT scans were performed at baseline and after 6, 12, and 24 months of treatment and were analyzed with Mindways QCT-PRO BIT software. Minimum and maximum section modulus, buckling ratio (BR), and cross-sectional area (CSA) were calculated as measurements of bending strength, risk of buckling, and bone apposition, respectively. After 24 months of TPTD treatment, areal and volumetric FN BMD increased significantly by 4.0% and 3.0%, respectively, compared with baseline. Decreases in cortical volumetric BMD occurred in locations not adversely affecting minimum bending strength indicators. Cortical CSA increased by 4.3%, whereas total CSA remained unchanged over the study duration, indicating that endosteal but no periosteal growth was observed. Strength parameters for buckling did not change at 6 and 12 months but improved significantly at 24 months. Measures of bending strength showed a trend toward improvement. Changes tended to be larger in individuals at higher risk of buckling failure. Prior antiresorptive treatment may delay response to TPTD, but based on the small magnitude of the mostly insignificant changes at 6 months, this does not appear to lead to an interim phase of reduced bone strength. In summary, FN QCT provides a tool for detailed longitudinal investigation of bone strength indices in vivo for different loading modes, yields insight into underlying structural changes, and provides relevant mechanostructural information beyond dual-energy X-ray absorptiometry. Continuous TPTD treatment for 24 months improves FN bone strength parameters.
机译:我们基于接受特立帕肽(TPTD)的受试者的股骨颈(FN)的3D定量计算机断层扫描(QCT)研究了骨骼分布,几何形状和骨骼强度的变化。分析了52名绝经后严重骨质疏松症妇女。根据患者先前使用骨质疏松症药物的治疗方法将其分为三个亚组:未接受过治疗(未接受过Tx; n = 8),已接受过治疗(未接受过Tx; n = 12)和经过预处理对治疗反应不佳的患者(未接受过治疗)。 pre-Tx; n = 32)。 QCT扫描是在基线以及治疗6、12和24个月后进行的,并使用Mindways QCT-PRO BIT软件进行了分析。计算最小和最大截面模量,屈曲比(BR)和横截面积(CSA),分别作为抗弯强度,屈曲风险和骨并置的量度。 TPTD治疗24个月后,与基线相比,面积和体积FN BMD分别显着增加了4.0%和3.0%。皮质体积BMD的降低发生在不会对最小弯曲强度指标产生不利影响的位置。在研究期间,皮质CSA增加了4.3%,而总CSA则保持不变,这表明骨内膜未见骨膜生长。屈曲强度参数在6和12个月时没有变化,但在24个月时显着改善。弯曲强度的测量显示出改善的趋势。具有较高屈曲失败风险的人的变化趋势往往更大。先前的抗吸收治疗可能会延迟对TPTD的反应,但是基于在6个月时几乎无明显变化的小幅度变化,这似乎并未导致骨强度降低的中期阶段。总而言之,FN QCT提供了一种工具,用于详细纵向研究不同负荷模式下的体内骨骼强度指标,深入了解潜在的结构变化,并提供双能量X射线吸收法以外的相关机械结构信息。连续TPTD治疗24个月可改善FN骨强度参数。

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