人类小梁骨的亚小梁应变演化和骨折标准

M. Turunen, S. Cann, Erika Tudisco, G. Lovric, A. Patera, S. Hall, H. Isaksson
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引用次数: 0

摘要

要了解骨折背后最有害的特征,关键是要了解局部应变极限及其与局部和全局破坏地点的关系。数字体积相关是一种新兴的研究骨小梁结构在载荷作用下应变的技术。本研究的目的是在不同的图像分辨率下研究骨小梁组织的三维应变分布和骨小梁下水平的损伤判据。人类尸体小梁骨样本在原位压缩直到失效,同时用高分辨率同步辐射x射线断层扫描成像。数字体积相关性用于确定裂纹(即将发生断裂的地方)和非裂纹区域小梁内的应变。骨组织可以承受局部非常高的压缩或拉伸应变(~10%),而不会立即导致骨折。因此,在发展裂缝附近的局部应变高于先前报道的整个小梁结构,与报道的单个孤立小梁相似。目前研究骨折在组织水平的文献似乎低估了在小梁骨的最大应变量级。同样,当我们缩小图像(降低分辨率)时,我们报告了更低的应变;这表明,观察到的菌株依赖于它们被研究的分辨率。此外,裂纹区域的局部应变大小与整体参数(整体屈服应变、平均组织矿物质密度和骨体积分数)相关。小梁的厚度似乎是一个重要的预测结构会在哪里断裂,因为它在最薄弱的环节失效。综上所述,本研究首次以亚小梁分辨率对人骨小梁结构中的局部应变进行了研究,证实了单个小梁在载荷作用下的高应变量级,更重要的是将其推广到整个小梁结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sub-Trabecular Strain Evolution and Fracture Criteria in Human Trabecular Bone
To understand the most detrimental characteristics behind bone fractures, it is key to understand the local strain limits and its relation to failure sites locally and globally. Digital volume correlation is an emerging technique to study strains in the trabecular bone structure under loading. The aim of this study was to investigate the three-dimensional strain distributions as well as damage criterion at the sub-trabecular level in trabecular bone tissue using different image resolutions. Human cadaver trabecular bone samples were compressed in situ until failure, while imaging with high-resolution synchrotron radiation X-ray tomography. Digital volume correlation was used to determine the strains inside the trabeculae in cracking (where fractures are about to occur) and non-cracking regions. Bone tissue was found to withstand locally very high compressive or tensile strains (~10%) without immediately resulting in a fracture. Thus, local strains in close vicinity of developing cracks were higher than previously reported for a whole trabecular structure and similar as reported for single isolated trabeculae. Current literature investigating bone fractures at the tissue level seem to underestimate the maximum strain magnitudes in trabecular bone. We similarly report lower strains when downscaling our images (reducing the resolution); this suggests that the observed strains are dependent on the resolution at which they are investigated. Furthermore, the local strain magnitudes at the crack regions correlate with global parameters (global yield strain, average tissue mineral density and bone volume fraction). The trabecular thickness appears to be an important predictor for where the structure will break, as it fails at the weakest link. In summary, this first study to investigate the local strains in a trabecular structure at sub-trabecula resolution in human bone confirms the high strain magnitudes reported for single trabeculae under loading and more importantly extends the translation to the whole trabecular structure.
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