Pistoia W, van Rietbergen B, Rüegsegger P
Institute for Biomedical Engineering, University of Zürich and Swiss Federal Institute of Technology (ETH), Moussonstrasse 18, CH-8044 Zürich, Switzerland.
Bone. 2003 Dec;33(6):937-45. doi: 10.1016/j.bone.2003.06.003.
Metabolic bone diseases such as osteoporosis usually cause a decrease in bone mass and a deterioration of bone microarchitecture leading to a decline in bone strength. Methods to predict bone strength in patients are currently based on bone mass only. It has been suggested that an improved prediction of bone strength might be possible if structural changes are taken into account as well. In this study we evaluated which structural parameters (other than bone mass) are the best predictors for changes in bone mechanical properties of the human radius after different bone atrophy scenarios and whether the original strength of the affected bone can be recovered if bone loss is restored by thickening of the remaining structures. To answer these questions, a human radius was measured with a microcomputer tomography scanner to extract the full three-dimensional architecture of the distal radius at an isotropic resolution of 80 microm. Eight models with modified bone architecture were created and the mechanical variations due to these modifications were studied using microfinite element (micro-FE) simulations. In four models mass was lowered by 20%, either by reducing cortical thickness, trabecular thickness, or number of trabeculae or by overall thinning of structures. In the other four models bone mass was restored to the original value using a trabecular bone thickening procedure. The micro-FE analyses revealed that most load was carried by the cortical bone. For this reason, bone strength was affected most in the reduced cortical thickness model. For the same reason, the trabecular bone atrophy scenarios, all of which affected bone strength in a very similar way, resulted in less dramatic bone strength reduction. The restoration of bone mass did not recover the original bone strength. These findings demonstrate that the importance of different parameters for the prediction of bone strength also depends on the mechanical loading. This could explain why results of earlier studies on the importance of structural parameters can be inconsistent and site-dependent.
骨质疏松症等代谢性骨病通常会导致骨量减少和骨微结构恶化,进而导致骨强度下降。目前,预测患者骨强度的方法仅基于骨量。有人提出,如果同时考虑结构变化,可能会更好地预测骨强度。在本研究中,我们评估了哪些结构参数(除骨量外)是不同骨萎缩情况后人桡骨骨力学性能变化的最佳预测指标,以及如果通过增厚剩余结构来恢复骨丢失,受影响骨骼的原始强度是否能够恢复。为了回答这些问题,我们使用微型计算机断层扫描仪对人桡骨进行测量,以80微米的各向同性分辨率提取桡骨远端的完整三维结构。创建了八个具有修改后骨结构的模型,并使用微观有限元(micro-FE)模拟研究了这些修改导致的力学变化。在四个模型中,通过减少皮质厚度、小梁厚度或小梁数量或整体结构变薄,使骨量降低20%。在另外四个模型中,使用小梁骨增厚程序将骨量恢复到原始值。微观有限元分析表明,大部分载荷由皮质骨承担。因此,在皮质厚度减少的模型中,骨强度受影响最大。出于同样的原因,小梁骨萎缩情况虽然都以非常相似的方式影响骨强度,但导致的骨强度降低幅度较小。骨量的恢复并没有恢复原始骨强度。这些发现表明,不同参数对骨强度预测的重要性也取决于机械载荷。这可以解释为什么早期关于结构参数重要性的研究结果可能不一致且因部位而异。