Effect of trabecular architectures on the mechanical response in osteoporotic and healthy human bone

被引:5
|
作者
Bregoli, Chiara [1 ,2 ]
Biffi, Carlo Alberto [1 ]
Tuissi, Ausonio [1 ]
Buccino, Federica [2 ,3 ]
机构
[1] CNR, CNR ICMTE, Lecce, Italy
[2] Politecn Milan, Mech Engn Dept, Milan, Italy
[3] IRCCS Ist Ortoped Galeazzi, Milan, Italy
关键词
Human trabecular bone; Morphometric parameters; Mutual relationships; Bone mechanical behaviour; Computational mesoscale models; CANCELLOUS BONE; ELASTIC PROPERTIES; QUANTIFICATION; FEMUR;
D O I
10.1007/s11517-024-03134-8
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
Research at the mesoscale bone trabeculae arrangement yields intriguing results that, due to their clinical resolution, can be applied in clinical field, contributing significantly to the diagnosis of bone-related diseases. While the literature offers quantitative morphometric parameters for a thorough characterization of the mesoscale bone network, there is a gap in understanding relationships among them, particularly in the context of various bone pathologies. This research aims to bridge these gaps by offering a quantitative evaluation of the interplay among morphometric parameters and mechanical response at mesoscale in osteoporotic and non-osteoporotic bones. Bone mechanical response, dependent on trabecular arrangement, is defined by apparent stiffness, computationally calculated using the Gibson-Ashby model. Key findings indicate that: (i) in addition to bone density, measured using X-ray absorptiometry, trabecular connectivity density, trabecular spacing and degree of anisotropy are crucial parameters for characterize osteoporosis state; (ii) apparent stiffness values exhibit strong correlations with bone density and connectivity density; (iii) connectivity density and degree of anisotropy result the best predictors of mechanical response. Despite the inherent heterogeneity in bone structure, suggesting the potential benefit of a larger sample size in the future, this approach presents a valuable method to enhance discrimination between osteoporotic and non-osteoporotic samples.
引用
收藏
页码:3263 / 3281
页数:19
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