Malekipour Fatemeh, Oetomo Denny, Lee Peter Vee-Sin
Department of Mechanical Engineering, Melbourne School of Engineering, University of Melbourne, Australia.
Department of Mechanical Engineering, Melbourne School of Engineering, University of Melbourne, Australia.
J Biomech. 2017 Apr 11;55:85-91. doi: 10.1016/j.jbiomech.2017.02.005. Epub 2017 Feb 21.
Subchondral bone (SCB) microdamage is commonly observed in traumatic joint injuries and has been strongly associated with post-traumatic osteoarthritis (PTOA). Knowledge of the three-dimensional stress and strain distribution within the SCB tissue helps to understand the mechanism of SCB failure, and may lead to an improved understanding of mechanisms of PTOA initiation, prevention and treatment. In this study, we used high-resolution micro-computed tomography (µCT)-based finite element (FE) modelling of cartilage-bone to evaluate the failure mechanism and the locations of SCB tissue at high-risk of initial failure under compression. The µCT images of five cartilage-bone specimens with an average SCB thickness of 1.23±0.20mm were used to develop five µCT-based FE models. The FE models were analysed under axial compressions of approximately 30MPa applied to the cartilage surface while the bone edges were constrained. Strain and stress-based failure criteria were then applied to evaluate the failure mechanism of the SCB tissue under excessive compression through articular cartilage. µCT-based FE models predicted two locations in the SCB at high-risk of initial failure: (1) the interface of the calcified-uncalcified cartilage due to excessive tension, and (2) the trabecular bone beneath the subchondral plate due to excessive compression. µCT-based FE models of cartilage-bone enabled us to quantify the distribution of the applied compression which was transferred through the articular cartilage to its underlying SCB, and to investigate the mechanism and the mode of SCB tissue failure. Ultimately, the results will help to understand the mechanism of injury formation in relation to PTOA.
软骨下骨(SCB)微损伤在创伤性关节损伤中很常见,并且与创伤后骨关节炎(PTOA)密切相关。了解SCB组织内的三维应力和应变分布有助于理解SCB破坏的机制,并可能有助于更好地理解PTOA的发病、预防和治疗机制。在本研究中,我们使用基于高分辨率显微计算机断层扫描(µCT)的软骨-骨有限元(FE)模型来评估压缩状态下SCB组织的破坏机制和初始破坏高风险位置。使用五个平均SCB厚度为1.23±0.20mm的软骨-骨标本的µCT图像来建立五个基于µCT的FE模型。在对软骨表面施加约30MPa的轴向压缩且骨边缘受约束的情况下对FE模型进行分析。然后应用基于应变和应力的破坏标准来评估SCB组织在通过关节软骨的过度压缩下的破坏机制。基于µCT的FE模型预测了SCB中两个初始破坏高风险位置:(1)由于过度拉伸导致的钙化-未钙化软骨界面,以及(2)由于过度压缩导致的软骨下板下方的小梁骨。基于µCT的软骨-骨FE模型使我们能够量化通过关节软骨传递到其下方SCB的外加压缩分布,并研究SCB组织的破坏机制和模式。最终,这些结果将有助于理解与PTOA相关的损伤形成机制。