Division of Rheumatology, Department of Internal Medicine, Rush University Medical College, Chicago, IL, United States.
University of Pennsylvania School of Engineering and Applied Sciences, Philadelphia, PA 19104, United States.
Osteoarthritis Cartilage. 2024 Oct;32(10):1273-1282. doi: 10.1016/j.joca.2024.05.006. Epub 2024 May 31.
Synovial pathology has been linked to osteoarthritis (OA) pain in patients. Microscopic grading systems for synovial changes in human OA have been described, but a standardized approach for murine models of OA is needed. We sought to develop a reproducible approach and set of minimum recommendations for reporting of synovial histopathology in mouse models of OA.
Coronal and sagittal sections from male mouse knee joints subjected to destabilization of medial meniscus (DMM) or partial meniscectomy (PMX) were collected as part of other studies. Stains included Hematoxylin and Eosin (H&E), Toluidine Blue (T-Blue), and Safranin O/Fast Green (Saf-O). Four blinded readers graded pathological features (hyperplasia, cellularity, and fibrosis) at specific anatomic locations. Inter-reader agreement of each feature score was determined.
There was acceptable to very good agreement when using 3-4 individual readers. After DMM and PMX, expected medial predominant changes in hyperplasia and cellularity were observed, with fibrosis noted at 12 weeks post-PMX. Synovial changes were consistent from section to section in the mid-joint area. When comparing stains, H&E and T-blue resulted in better agreement compared to Saf-O stain.
To account for the pathologic and anatomic variability in synovial pathology and allow for a more standardized evaluation that can be compared across studies, we recommend evaluating a minimum set of 3 pathological features at standardized anatomic areas. Further, we suggest reporting individual feature scores separately before relying on a single summed "synovitis" score. H&E or T-blue are preferred, inter-reader agreement for each feature should be considered.
滑膜病理学与骨关节炎(OA)患者的疼痛有关。已经描述了人类 OA 滑膜变化的微观分级系统,但需要一种标准化的 OA 鼠模型方法。我们试图开发一种可重复的方法,并为 OA 鼠模型滑膜组织病理学报告制定一套最低建议。
作为其他研究的一部分,收集了接受内侧半月板不稳定(DMM)或部分半月板切除术(PMX)的雄性小鼠膝关节的冠状和矢状切片。染色包括苏木精和伊红(H&E)、甲苯胺蓝(T-Blue)和番红 O/固绿(Saf-O)。四名盲法读者对特定解剖部位的病理特征(增生、细胞密度和纤维化)进行分级。确定每个特征评分的读者间一致性。
使用 3-4 名独立读者时,具有可接受至非常好的一致性。在 DMM 和 PMX 之后,观察到预期的内侧增生和细胞密度为主的变化,在 PMX 后 12 周时观察到纤维化。在关节中部区域,滑膜变化在各切片之间具有一致性。在比较染色时,H&E 和 T-blue 比 Saf-O 染色产生更好的一致性。
为了考虑滑膜病理学的病理和解剖变异性,并允许更标准化的评估,以便在研究之间进行比较,我们建议在标准化解剖区域评估至少 3 种病理特征。此外,我们建议在依赖单个综合“滑膜炎”评分之前,分别报告各个特征评分。建议报告单独的特征分数,在评估滑膜病理学时,H&E 或 T-blue 是首选,读者间的一致性也应该被考虑。