Department of Diagnostic and Interventional Radiology, Aachen University Hospital, Aachen, Germany.
Medical Faculty, Department of Diagnostic and Interventional Radiology, University Hospital Düsseldorf, Moorenstraße 5, 40225, Dusseldorf, Germany.
Sci Rep. 2020 Sep 15;10(1):15106. doi: 10.1038/s41598-020-72208-y.
Water, collagen, and proteoglycans determine articular cartilage functionality. If altered, susceptibility to premature degeneration is increased. This study investigated the effects of enzymatic proteoglycan depletion on cartilage functionality as assessed by advanced Magnetic Resonance Imaging (MRI) techniques under standardized loading. Lateral femoral condylar cartilage-bone samples from patients undergoing knee replacement (n = 29) were serially imaged by Proton Density-weighted and T1, T1ρ, T2, and T2* mapping sequences on a clinical 3.0 T MRI scanner (Achieva, Philips). Using pressure-controlled indentation loading, samples were imaged unloaded and quasi-statically loaded to 15.1 N and 28.6 N, and both before and after exposure to low-concentrated (LT, 0.1 mg/mL, n = 10) or high-concentrated trypsin (HT, 1.0 mg/mL, n = 10). Controls were not treated (n = 9). Responses to loading were assessed for the entire sample and regionally, i.e. sub- and peri-pistonally, and zonally, i.e. upper and lower sample halves. Trypsin effects were quantified as relative changes (Δ), analysed using appropriate statistical tests, and referenced histologically. Histological proteoglycan depletion was reflected by significant sub-pistonal decreases in T1 (p = 0.003) and T2 (p = 0.008) after HT exposure. Loading-induced changes in T1ρ and T2* were not related. In conclusion, proteoglycan depletion alters cartilage functionality and may be assessed using serial T1 and T2 mapping under loading.
水、胶原蛋白和蛋白聚糖决定了关节软骨的功能。如果发生改变,软骨过早退化的易感性将会增加。本研究采用先进的磁共振成像(MRI)技术,在标准化加载条件下,研究了酶解蛋白聚糖耗竭对软骨功能的影响。对 29 例行膝关节置换术患者的股骨外侧髁软骨-骨样本进行连续 MRI 成像,采用质子密度加权和 T1、T1ρ、T2 和 T2成像序列,使用压力控制的压痕加载,在临床 3.0T MRI 扫描仪(Achieva,Philips)上对样本进行未加载和准静态加载至 15.1N 和 28.6N,以及在暴露于低浓度(LT,0.1mg/mL,n=10)或高浓度(HT,1.0mg/mL,n=10)胰蛋白酶前后进行成像。对照组未进行处理(n=9)。评估整个样本和亚区、即亚活塞区和活塞周围区以及分区、即上下样本半区的加载响应。采用适当的统计检验分析相对变化(Δ),并参考组织学进行定量分析。HT 暴露后,T1(p=0.003)和 T2(p=0.008)的亚活塞下明显减少反映了组织学上的蛋白聚糖耗竭。T1ρ和 T2的加载诱导变化之间没有相关性。总之,蛋白聚糖耗竭改变了软骨功能,并且可以通过在加载下进行连续 T1 和 T2 映射来评估。