Department of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands.
Osteoarthritis Cartilage. 2013 Feb;21(2):331-8. doi: 10.1016/j.joca.2012.10.013. Epub 2012 Nov 7.
OBJECTIVE: Osteoarthritis (OA) is characterized by loss of cartilage and alterations in subchondral bone architecture. Changes in cartilage and bone tissue occur simultaneously and are spatially correlated, indicating that they are probably related. We investigated two hypotheses regarding this relationship. According to the first hypothesis, both wear and tear changes in cartilage, and remodeling changes in bone are a result of abnormal loading conditions. According to the second hypothesis, loss of cartilage and changes in bone architecture result from endochondral ossification. DESIGN: With an established bone adaptation model, we simulated adaptation to high load and endochondral ossification, and investigated whether alterations in bone architecture between these conditions were different. In addition, we analyzed bone structure differences between human bone samples with increasing degrees of OA, and compared these data to the simulation results. RESULTS: The simulation of endochondral ossification led to a more refined structure, with a higher number of trabeculae in agreement with the finding of a higher trabecular number in osteochondral plugs with severe OA. Furthermore, endochondral ossification could explain the presence of a "double subchondral plate" which we found in some human bone samples. However, endochondral ossification could not explain the increase in bone volume fraction that we observed, whereas adaptation to high loading could. CONCLUSION: Based on the simulation and experimental data, we postulate that both endochondral ossification and adaptation to high load may contribute to OA bone structural changes, while both wear and tear and the replacement of mineralized cartilage with bone tissue may contribute cartilage thinning.
目的:骨关节炎(OA)的特征是软骨丧失和软骨下骨结构改变。软骨和骨组织的变化同时发生且具有空间相关性,表明它们可能相关。我们研究了这一关系的两个假设。根据第一个假设,软骨的磨损和撕裂变化以及骨的重塑变化都是异常负荷条件的结果。根据第二个假设,软骨的丧失和骨结构的改变是由软骨内成骨引起的。
设计:我们利用已建立的骨适应模型,模拟了高负荷和软骨内成骨的适应过程,并研究了这两种情况下骨结构的改变是否不同。此外,我们分析了不同程度 OA 的人骨样本之间的骨结构差异,并将这些数据与模拟结果进行比较。
结果:软骨内成骨的模拟导致了更精细的结构,具有更多的小梁,与严重 OA 的骨软骨塞中较高的小梁数一致。此外,软骨内成骨可以解释我们在一些人骨样本中发现的“双层软骨下板”的存在。然而,软骨内成骨不能解释我们观察到的骨体积分数的增加,而高负荷适应可以。
结论:基于模拟和实验数据,我们假设软骨内成骨和高负荷适应都可能导致 OA 骨结构变化,而磨损和撕裂以及矿化软骨被骨组织替代可能导致软骨变薄。
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