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μFEA 成功地在整个椎体的微损伤区域表现出更高的应力和应变。

μFEA successfully exhibits higher stresses and strains in microdamaged regions of whole vertebrae.

机构信息

Orthopaedic Biomechanics Laboratory, Sunnybrook Research Institute, 2075 Bayview Avenue, S620, Toronto, ON, Canada, M4N3M5.

出版信息

J Orthop Res. 2013 Oct;31(10):1653-60. doi: 10.1002/jor.22392. Epub 2013 Jun 4.

Abstract

Micro-finite element (μFE) modeling has shown promise in evaluating the structural integrity of trabecular bone. Histologic microcrack analyses have been compared to μFE models of trabecular bone cores to demonstrate the potential of this technique. To date this has not been achieved in whole bone structures, and comparisons of histologic microcrack and μFE results have been limited due to challenges in alignment of 2D sections with 3D data sets. The goal of this study was to ascertain if image registration can facilitate determination of a relationship between stresses and strains generated from μFE models of whole vertebrae and histologically identified microdamage. μFE models of three whole vertebrae, stained sequentially with calcein and fuchsin, were generated with accurate integration of element sets representing the histologic sections based on volumetric image registration. Displacement boundary conditions were applied to the μFE models based on registration of loaded and unloaded μCT images. Histologically labeled damaged regions were found to have significantly higher von Mises stresses and principle strains in the μFE models, as compared to undamaged regions. This work provides a new robust method for generating and histologically validating μFE models of whole bones that can represent trabecular damage resulting from complex physiologic loading.

摘要

微有限元(μFE)建模在评估小梁骨的结构完整性方面显示出了潜力。已经对组织学微裂纹分析与小梁骨芯的 μFE 模型进行了比较,以证明该技术的潜力。迄今为止,尚未在整个骨结构中实现这一目标,并且由于二维切片与三维数据集之间的对齐挑战,组织学微裂纹和 μFE 结果的比较受到限制。本研究的目的是确定图像配准是否可以促进确定整个椎体的 μFE 模型和组织学确定的微损伤产生的应力和应变之间的关系。使用基于体积图像配准的组织学切片的元素集的精确集成,生成了三个整个椎体的 μFE 模型,这些椎体用钙黄绿素和品红依次染色。基于加载和未加载 μCT 图像的配准,向 μFE 模型施加位移边界条件。与未损坏区域相比,在 μFE 模型中,组织学标记的受损区域的 von Mises 应力和主应变明显更高。这项工作提供了一种新的强大方法,用于生成和组织学验证整个骨骼的 μFE 模型,这些模型可以代表复杂生理负荷引起的小梁损伤。

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