Joint and Soft Tissue Unit, Department of Clinical Sciences Malmö, Lund University, Department of Orthopaedics, Skåne University Hospital, Malmö, SE-20502 Malmö, Sweden.
Joint and Soft Tissue Unit, Department of Clinical Sciences Malmö, Lund University, Department of Orthopaedics, Skåne University Hospital, Malmö, SE-20502 Malmö, Sweden; Department of Diagnostic Radiology, Oulu University Hospital, POB 50, FI-90029 OYS, Oulu, Finland.
Osteoarthritis Cartilage. 2012 May;20(5):396-404. doi: 10.1016/j.joca.2012.01.015. Epub 2012 Feb 11.
This study investigates sulphated glycosaminoglycans (sGAG) content changes in early osteoarthritis (OA), and whether contrast-enhanced magnetic resonance imaging (MRI) of cartilage in vitro may identify early event of OA pathology.
Osteochondral plugs from patients with hip OA or femoral neck fracture (reference group) were collected and analysed by 1.5 T MRI with ΔR1 as a measure of cartilage contrast concentration. Cartilage hydration, contents of sGAG, cartilage oligomeric matrix protein (COMP), hydroxyproline, denatured collagen, and aggrecan TEGE(392) neoepitope were determined and histological grading was performed.
sGAG content correlated to ΔR1, although no difference in either of these parameters was detectable between OA and reference cartilage at 4 h of contrast equilibration. In contrast, biochemical analysis of other cartilage matrix constituents showed distinct alterations typical for early cartilage degradation in OA cartilage and with clear evidence for increased aggrecan turnover.
In the present in vitro study, cartilage sGAG content could not distinguish between early OA cartilage and reference cartilage. Given, that delayed gadolinium enhanced MRI of cartilage (dGEMRIC) indicates early events in the pathogenesis of OA in vivo, our results from the in vitro studies imply other, additional factors than cartilage sGAG content, e.g., alterations in diffusion or increased supply of contrast agent in the diseased joint. Alternatively, an altered dGEMRIC reflects later stages of OA, when sGAG content decreases. Further investigations are warranted, to understand variations in sGAG content in pathology, an essential background for interpreting dGEMRIC measurements.
本研究旨在探讨早期骨关节炎(OA)中硫酸化糖胺聚糖(sGAG)含量的变化,以及体外对比增强磁共振成像(MRI)能否识别 OA 病理的早期事件。
从髋 OA 或股骨颈骨折患者(参照组)中采集骨软骨栓,并通过 1.5T MRI 进行分析,以 ΔR1 作为软骨对比浓度的衡量标准。测定软骨水合作用、sGAG 含量、软骨寡聚基质蛋白(COMP)、羟脯氨酸、变性胶原和聚集蛋白 TEGE(392)新表位,并进行组织学分级。
sGAG 含量与 ΔR1 相关,但在对比平衡 4 小时时,OA 软骨和参照软骨之间在这些参数中均未检测到差异。相比之下,其他软骨基质成分的生化分析显示,OA 软骨中存在典型的早期软骨降解,并有明确证据表明聚集蛋白周转率增加,这表明存在明显的改变。
在本体外研究中,软骨 sGAG 含量无法区分早期 OA 软骨和参照软骨。鉴于体内延迟钆增强 MRI 软骨(dGEMRIC)可指示 OA 发病机制的早期事件,我们的体外研究结果表明,除了软骨 sGAG 含量外,还有其他因素(如扩散改变或病变关节中对比剂供应增加)会导致这种情况。或者,dGEMRIC 反映了 OA 的后期阶段,此时 sGAG 含量降低。需要进一步研究,以了解病理学中 sGAG 含量的变化,这是解释 dGEMRIC 测量结果的必要背景。