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High resolution quantitative computed tomography-based assessment of trabecular microstructure and strength estimates by finite-element analysis of the spine, but not DXA, reflects vertebral fracture status in men with glucocorticoid-induced osteoporosis

机译:高分辨率定量计算的基于分层的脊柱细胞微观结构和强度估算的评估,但不是DXA,反映了糖皮质激素诱导的骨质疏松症的男性椎骨骨折状态

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摘要

The current gold-standard for the diagnosis of osteoporosis, dual x-ray absorptiometry (DXA), measures areal projected bone mineral density (aBMD). Besides including projection artifacts, DXA does not allow assessment of the spatial distribution of BMD within the bone or aspects of bone quality, such as trabecular microstructure. Although the WHO definition of osteoporosis based on DXA correlates well with fracture risk in women with postmenopausal osteoporosis , the majority of fractures occur in women who are not classified as osteoporotic by this criterion . Absolute fracture risk models that capture a number of independent risk factors, such as prevalent fractures or age, show that DXA has limitations in assessing bone strength and the corresponding fracture risk.
机译:目前的核对骨质疏松症诊断的金标准,双X射线吸收测量(DXA),测量面积突出的骨密度(ABMD)。 此外,除了包括投影伪影之外,DXA不允许评估BMD在骨骼质量的骨骼或方面内的空间分布,例如小梁微观结构。 尽管基于DXA的骨质疏松症的定义与患有绝经后骨质疏松症的女性的骨折风险相比,但大多数骨折发生在未被本标准被疏松疏松症的女性发生。 绝对骨折风险模型,捕获许多独立风险因素,例如普遍的骨折或年龄,表明DXA具有评估骨骼强度和相应的骨折风险的局限性。

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