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首页> 外文期刊>Osteoarthritis and cartilage >Depth-wise progression of osteoarthritis in human articular cartilage: investigation of composition, structure and biomechanics.
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Depth-wise progression of osteoarthritis in human articular cartilage: investigation of composition, structure and biomechanics.

机译:人关节软骨中骨关节炎的深度进展:组成,结构和生物力学研究。

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OBJECTIVE: Osteoarthritis (OA) is characterized by the changes in structure and composition of articular cartilage. However, it is not fully known, what is the depth-wise change in two major components of the cartilage solid matrix, i.e., collagen and proteoglycans (PGs), during OA progression. Further, it is unknown how the depth-wise changes affect local tissue strains during compression. Our aim was to address these issues. METHODS: Data from the previous microscopic and biochemical measurements of the collagen content, distribution and orientation, PG content and distribution, water content and histological grade of normal and degenerated human patellar articular cartilage (n=73) were reanalyzed in a depth-wise manner. Using this information, a composition-based finite element (FE) model was used to estimate tissue function solely based on its composition and structure. RESULTS: The orientation angle of collagen fibrils in the superficial zone of cartilage was significantly less parallel to the surface (P<0.05) in samples with early degeneration than in healthy samples. Similarly, PG content was reduced in the superficial zone in early OA (P<0.05). However, collagen content decreased significantly only at the advanced stage of OA (P<0.05). The composition-based FE model showed that under a constant stress, local tissue strains increased as OA progressed. CONCLUSION: For the first time, depth-wise point-by-point statistical comparisons of structure and composition of human articular cartilage were conducted. The present results indicated that early OA is primarily characterized by the changes in collagen orientation and PG content in the superficial zone, while collagen content does not change until OA has progressed to its late stage. Our simulation results suggest that impact loads in OA joint could create a risk for tissue failure and cell death.
机译:目的:骨关节炎(OA)的特征是关节软骨的结构和组成发生变化。然而,尚不完全清楚在OA进展过程中,软骨固体基质的两个主要成分即胶原蛋白和蛋白聚糖(PGs)的深度变化是什么。此外,未知深度方向的变化如何在压缩期间影响局部组织应变。我们的目的是解决这些问题。方法:从以前的显微镜和生化测量中,对正常和退化的人pa骨关节软骨(n = 73)的胶原蛋白含量,分布和方向,PG含量和分布,水含量和组织学等级的显微和生化测量数据进行了深度分析。 。使用此信息,仅基于组织的组成和结构,可以使用基于组成的有限元(FE)模型来估计组织功能。结果:与健康样品相比,具有早期变性的样品中胶原纤维在软骨表层的取向角与表面的平行性显着降低(P <0.05)。同样,在早期OA中浅表区的PG含量降低(P <0.05)。然而,胶原蛋白含量仅在OA晚期才显着下降(P <0.05)。基于成分的有限元模型表明,在恒定应力下,局部组织应变随着OA的发展而增加。结论:首次进行了逐点统计的人体关节软骨结构和组成的统计比较。目前的结果表明,早期OA的主要特征是表层区域胶原蛋白取向和PG含量的变化,而胶原蛋白的含量直到OA进展到晚期才发生变化。我们的模拟结果表明,OA关节的冲击负荷可能会导致组织衰竭和细胞死亡的风险。

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