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Automated method to measure trabecular thickness from microcomputed tomographic scans and its application

机译:微型计算机断层扫描自动测量骨小梁厚度的方法及其应用

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Trabeculae form the internal bony mesh work and provide strength to the bone; interconnectivity, overall density, and trabecular thickness are important measures of the integrity of the internal architecture. Such strength is achieved only gradually during ontogeny, whereby an increase in trabecular thickness precedes an increase in mineralization. Loss of bone mass later in life may be compensated for by thickening of the remaining trabeculae. These facts, and the role of trabeculae in mineral homeostasis, highlight the importance of investigating trabecular thickness within and between species. While nondestructive imaging techniques (i.e., mu CT and MRI) are becoming increasingly popular, quantification of trabecular thickness using nondestructive techniques has proved difficult owing to limitations imposed by scanning parameters, uniform thresholding, and partial volume averaging. Here we present a computer application, which aims to overcome these problems. Validation is carried out against a phantom and against trabecular thickness measured in corresponding histological sections. Good agreement was found between these measurements. Furthermore, when trabecular thickness is recorded for modern human fetal ilia, a trend toward trabecular thickness increase is found and is in line with reports of ontogenetic morphometric changes using histological sections. However, there are discrepancies. These may in part be due to partial volume effects of obliquely oriented structures. More crucial, however, are problems inherent in histological sections, e.g., shrinkage and distortion, especially where differences in mineralization are concerned; this may affect biological interpretations.
机译:小梁形成内部的骨网状结构并为骨骼提供强度。互连性,总体密度和小梁厚度是内部体系结构完整性的重要指标。这种强度仅在个体发育过程中逐渐达到,由此骨小梁厚度的增加先于矿化的增加。生命后期的骨量损失可以通过剩余小梁的增厚来补偿。这些事实以及小梁在矿物质体内稳态中的作用,突出了研究物种内和物种间小梁厚度的重要性。尽管无损成像技术(即mu CT和MRI)变得越来越普遍,但由于扫描参数,统一阈值和部分体积平均的限制,使用无损技术对小梁厚度进行量化已证明是困难的。在这里,我们提出了一种计算机应用程序,旨在克服这些问题。针对体模和在相应组织学切片中测量的小梁厚度进行验证。在这些测量之间发现良好的一致性。此外,当记录现代人胎儿fe骨的骨小梁厚度时,发现骨小梁厚度增加的趋势,并且与使用组织学切片的个体形态学形态变化的报道一致。但是,存在差异。这些可能部分是由于倾斜定向结构的部分体积效应引起的。然而,更为关键的是组织学方面固有的问题,例如收缩和变形,特别是在涉及矿化差异方面;这可能会影响生物学解释。

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