Department of Applied Physics, University of Eastern Finland, POB 1627, 70211, Kuopio, Finland.
Research Unit of Medical Imaging, Physics and Technology, Faculty of Medicine, University of Oulu, Oulu, Finland.
Ann Biomed Eng. 2020 Dec;48(12):2887-2900. doi: 10.1007/s10439-020-02559-0. Epub 2020 Jul 9.
Relationships between composition, structure and constituent-specific functional properties of human articular cartilage at different stages of osteoarthritis (OA) are poorly known. We established these relationships by comparison of elastic, viscoelastic and fibril-reinforced poroelastic mechanical properties with microscopic and spectroscopic analysis of structure and composition of healthy and osteoarthritic human tibial cartilage (n = 27). At a low frequency (0.005 Hz), proteoglycan content correlated negatively and collagen content correlated positively with the phase difference (i.e. tissue viscosity). At a high-frequency regime (> 0.05 Hz), proteoglycan content correlated negatively and collagen orientation angle correlated positively with the phase difference. Proteoglycans were lost in the early and advanced OA groups compared to the healthy group, while the superficial collagen orientation angle was greater only in the advanced OA group compared to the healthy group. Simultaneously, the initial fibril network modulus (fibril pretension) was smaller in the early and advanced OA groups compared to the healthy group. These findings suggest different mechanisms contribute to cartilage viscosity in low and high frequencies, and that the loss of superficial collagen pretension during early OA is due to lower tissue swelling (PG loss), while in advanced OA, both collagen disorganization and lower swelling modulate the collagen fibril pretension.
在不同阶段的骨关节炎(OA)中,关节软骨的组成、结构和成分特异性功能特性之间的关系知之甚少。我们通过比较健康和骨关节炎人类胫骨软骨的弹性、粘弹性和纤维增强多孔弹性力学性能,以及结构和组成的微观和光谱分析,建立了这些关系(n = 27)。在低频(0.005 Hz)下,糖胺聚糖含量与相位差(即组织粘度)呈负相关,而胶原蛋白含量与相位差呈正相关。在高频区(> 0.05 Hz),糖胺聚糖含量与相位差呈负相关,胶原蛋白取向角与相位差呈正相关。与健康组相比,早期和晚期 OA 组的糖胺聚糖丢失,而与健康组相比,仅晚期 OA 组的浅层胶原蛋白取向角更大。同时,与健康组相比,早期和晚期 OA 组的初始纤维网络模量(纤维预张力)较小。这些发现表明,在低频和高频下,软骨粘度的产生有不同的机制,并且在早期 OA 中,浅层胶原蛋白预张力的丧失是由于组织肿胀(PG 丢失)所致,而在晚期 OA 中,胶原的紊乱和较低的肿胀都会调节胶原纤维的预张力。