Ural Ani, Vashishth Deepak
Department of Biomedical Engineering, Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, 110 8th Street, Troy, New York 12180, USA.
J Biomech Eng. 2007 Oct;129(5):625-31. doi: 10.1115/1.2768377.
The extent to which increased intracortical porosity affects the fracture properties of aging and osteoporotic bone is unknown. Here, we report the development and application of a microcomputed tomography based finite element approach that allows determining the effects of intracortical porosity on bone fracture by blocking all other age-related changes in bone. Previously tested compact tension specimens from human tibiae were scanned using microcomputed tomography and converted to finite element meshes containing three-dimensional cohesive finite elements in the direction of the crack growth. Simulations were run incorporating age-related increase in intracortical porosity but keeping cohesive parameters representing other age-related effects constant. Additional simulations were performed with reduced cohesive parameters. The results showed a 6% decrease in initiation toughness and a 62% decrease in propagation toughness with a 4% increase in porosity. The reduction in toughnesses became even more pronounced when other age-related effects in addition to porosity were introduced. The initiation and propagation toughness decreased by 51% and 83%, respectively, with the combined effect of 4% increase in porosity and decrease in the cohesive properties reflecting other age-related changes in bone. These results show that intracortical porosity is a significant contributor to the fracture toughness of the cortical bone and that the combination of computational modeling with advanced imaging improves the prediction of the fracture properties of the aged and the osteoporotic cortical bone.
皮质内孔隙增加对衰老和骨质疏松性骨骨折特性的影响程度尚不清楚。在此,我们报告了一种基于微计算机断层扫描的有限元方法的开发与应用,该方法通过阻断骨中所有其他与年龄相关的变化来确定皮质内孔隙对骨折的影响。使用微计算机断层扫描对先前测试的来自人类胫骨的紧凑拉伸试样进行扫描,并转换为在裂纹扩展方向包含三维内聚有限元的有限元网格。进行模拟时纳入了与年龄相关的皮质内孔隙增加,但保持代表其他与年龄相关效应的内聚参数不变。使用降低的内聚参数进行了额外的模拟。结果显示,孔隙率增加4%时,起始韧性降低6%,扩展韧性降低62%。当除孔隙率外引入其他与年龄相关的效应时,韧性的降低变得更加明显。孔隙率增加4%与反映骨中其他与年龄相关变化的内聚性能降低的综合作用下,起始韧性和扩展韧性分别降低了51%和83%。这些结果表明,皮质内孔隙是皮质骨断裂韧性的重要贡献因素,并且计算建模与先进成像的结合改善了对衰老和骨质疏松性皮质骨骨折特性的预测。