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Quantifying Changes in the Bone Microarchitecture using Minkowski-Functionals and Scaling Vectors: a Comparative Study

机译:使用Minkowski-computionals和Scaling vectors量化骨微架构的变化:比较研究

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Osteoporosis is a metabolic bone disease leading to de-mineralization and increased risk of fracture. The two major factors that determine the biomechanical competence of bone are the degree of mineralization and the micro-architectural integrity. Today, modern imaging modalities exist that allow to depict structural details of trabecular bone tissue. Recently, non-linear techniques in 2D and 3D based on the scaling vector method (SVM) and the Minkowski functionals (MF) have been introduced, which show excellent performance in predicting bone strength and fracture risk. However, little is known about the performance of the various parameters with respect to monitoring structural changes due to progression of osteoporosis or as a result of medical treatment. We test and compare the two methodologies using realistic two-dimensional simulations of bone structures, which model the effect of osteoblasts and osteoclasts on the local change of relative bone density. The partial differential equations involved in the model are solved numerically using cellular automata (CA). Different realizations with slightly varying control parameters are considered. Our results show that even small changes in the trabecular structures, which are induced by variation of a control parameter of the system, become discernible by applying both the MF and the locally adapted scaling vector method. The results obtained with SVM are superior to those obtained with the Minkowski functionals. An additive combination of both measures drastically increases the sensitivity to slight changes in bone structures. These findings may be especially important for monitoring the treatment of patients, where the early recognition of (drug-induced) changes in the trabecular structure is crucial.
机译:骨质疏松症是一种代谢骨病,导致脱矿化和骨折风险增加。确定骨骼生物力学能力的两个主要因素是矿化程度和微观建筑完整性。如今,存在现代成像模式,其允许描绘小梁骨组织的结构细节。最近,已经介绍了基于缩放载体方法(SVM)和Minkowski功能(MF)的2D和3D中的非线性技术,这在预测骨强度和断裂风险方面具有出色的性能。然而,对于由于骨质疏松症的进展或药物治疗而导致的各种参数的性能几乎熟知。我们使用骨结构的现实二维模拟测试和比较两种方法,该方法模拟了成骨细胞和骨细胞对相对骨密度的局部变化的影响。模型中涉及的部分微分方程使用蜂窝自动机(CA)数值求解。考虑具有略微变化的控制参数的不同实现。我们的结果表明,通过系统的控制参数的变化引起的小梁结构的甚至小的变化也可以通过应用MF和本地适应的缩放矢量方法来辨别。用SVM获得的结果优于用Minkowski功能获得的结果。两种措施的添加剂组合大大增加了对骨结构微小变化的敏感性。这些发现对于监测患者的治疗可能尤为重要,其中患有小梁结构的早期识别(药物诱导的)变化至关重要。

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