Leskinen Henri P P, Tuppurainen Juuso, Jäntti Jiri, Mäkelä Janne T A, Nippolainen Ervin, Afara Isaac O, Töyräs Juha, Nykänen Olli, Nissi Mikko J
Department of Technical Physics, University of Eastern Finland, Yliopistonranta 8, 70210, Kuopio, Finland.
Mikkeli Central Hospital, Mikkeli, Finland.
Ann Biomed Eng. 2025 Jun 17. doi: 10.1007/s10439-025-03774-3.
Quantitative T2 mapping is an important MRI method for assessing degenerative changes in articular cartilage. Recently, in a measurement setup with automated sample re-orientation, it was demonstrated that T2 can be split into its orientation-independent components. This quantitative MRI study aims to assess the diagnostic significance of the automated approach with ex vivo human cartilage.
T2 maps of 30 human osteochondral samples harvested from 5 cadaveric individuals were acquired at 9.4T in 13 orientations, allowing calculation of the T2 components. Additionally, T1, adiabatic T1ρ, and continuous wave T1ρ with two spin-lock frequencies were scanned in a single orientation. For reference, the collagen network anisotropy, proteoglycan content and biomechanical indentation properties were measured. The relationships between quantitative MRI and reference parameters were studied using Mann-Whitney U-test and Spearman's rank correlation. All parameters were compared between healthy and degenerated groups based on OARSI grading.
The anisotropic relaxation rate component of T2 (R2a), and all T1 and T1ρ parameters differed (p < 0.05) between the groups in superficial cartilage. R2a correlated moderately with PLM anisotropy (r = 0.44) and optical density (r = - 0.37) in the deep zone. Isotropic T2 component (R2i) correlated with instantaneous modulus (r = 0.48), and R2a with phase shift between stress and strain during indentation testing (r = - 0.44). T1 and T1ρ parameters correlated with both, instantaneous and dynamic modulus in several zones of cartilage.
The elevation of T2 in degenerated cartilage is primarily driven by the R2a component, whereas the R2i component showed no significant difference between healthy and degenerated human articular cartilage.
定量T2映射是评估关节软骨退变的重要MRI方法。最近,在一个具有自动样本重新定向的测量设置中,已证明T2可分解为其与方向无关的分量。本定量MRI研究旨在评估自动方法对离体人软骨的诊断意义。
从5具尸体个体中采集30个人骨软骨样本的T2映射,在9.4T下于13个方向获取,从而能够计算T2分量。此外,在单个方向上扫描T1、绝热T1ρ以及具有两个自旋锁定频率的连续波T1ρ。作为参考,测量了胶原网络各向异性、蛋白聚糖含量和生物力学压痕特性。使用曼-惠特尼U检验和斯皮尔曼等级相关性研究定量MRI与参考参数之间的关系。基于OARSI分级,比较健康组和退变组之间的所有参数。
表层软骨组间T2的各向异性弛豫率分量(R2a)以及所有T1和T1ρ参数均存在差异(p < 0.05)。在深层区域,R2a与偏振光显微镜(PLM)各向异性(r = 0.44)和光密度(r = -0.37)呈中度相关。各向同性T2分量(R2i)与瞬时模量(r = 0.48)相关,而R2a与压痕测试期间应力和应变之间的相移相关(r = -0.44)。在软骨的几个区域,T1和T1ρ参数与瞬时模量和动态模量均相关。
退变软骨中T2的升高主要由R2a分量驱动,而R2i分量在健康和退变的人关节软骨之间无显著差异。