Department of Physics, University of Kuopio, Kuopio, Finland.
Osteoarthritis Cartilage. 2010 Jan;18(1):73-81. doi: 10.1016/j.joca.2009.08.003. Epub 2009 Aug 29.
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.
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.
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.
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.
骨关节炎(OA)的特征在于关节软骨的结构和组成发生变化。然而,OA 进展过程中软骨固基质的两个主要成分,即胶原和蛋白聚糖(PGs)的深度变化尚不完全清楚。此外,尚不清楚深度变化如何影响压缩过程中的局部组织应变。我们的目的是解决这些问题。
以前对正常和退变人髌骨关节软骨(n=73)的胶原含量、分布和取向、PG 含量和分布、水含量和组织学分级的微观和生化测量数据进行了深度重新分析。使用这些信息,基于组成的有限元(FE)模型仅基于其组成和结构来估计组织功能。
软骨浅层中胶原纤维的取向角与表面明显不平行(P<0.05),早期退变样本比健康样本更明显。同样,早期 OA 中浅层 PG 含量减少(P<0.05)。然而,仅在 OA 的晚期,胶原含量才显著降低(P<0.05)。基于组成的 FE 模型表明,在恒定应力下,随着 OA 的进展,局部组织应变增加。
首次对人关节软骨的结构和组成进行了深度逐点统计比较。目前的结果表明,早期 OA 主要表现为浅层胶原取向和 PG 含量的变化,而胶原含量直到 OA 进展到晚期才发生变化。我们的模拟结果表明,OA 关节中的冲击载荷可能会增加组织失效和细胞死亡的风险。