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膝关节骨关节炎的组织病理学亚组

Histopathological subgroups in knee osteoarthritis.

作者信息

Wyatt L A, Moreton B J, Mapp P I, Wilson D, Hill R, Ferguson E, Scammell B E, Walsh D A

机构信息

Arthritis Research UK Pain Centre, University of Nottingham, Nottingham, NG5 1PB, UK; Division of Rheumatology, Orthopaedics and Dermatology, University of Nottingham, Nottingham, UK.

Arthritis Research UK Pain Centre, University of Nottingham, Nottingham, NG5 1PB, UK; Division of Rehabilitation and Ageing, University of Nottingham, Nottingham, UK.

出版信息

Osteoarthritis Cartilage. 2017 Jan;25(1):14-22. doi: 10.1016/j.joca.2016.09.021. Epub 2016 Oct 6.

Abstract

OBJECTIVE

Osteoarthritis (OA) is a heterogeneous, multi-tissue disease. We hypothesised that different histopathological features characterise different stages during knee OA progression, and that discrete subgroups can be defined based on validated measures of OA histopathological features.

DESIGN

Medial tibial plateaux and synovium were from 343 post-mortem (PM) and 143 OA arthroplasty donations. A 'chondropathy/osteophyte' group (n = 217) was classified as PM cases with osteophytes or macroscopic medial tibiofemoral chondropathy lesions ≥grade 3 to represent pre-surgical (early) OA. 'Non-arthritic' controls (n = 48) were identified from the remaining PM cases. Mankin histopathological scores were subjected to Rasch analysis and supplemented with histopathological scores for subchondral bone marrow replacement and synovitis. Item weightings were derived by principle components analysis (PCA). Histopathological subgroups were sought using latent class analysis (LCA).

RESULTS

Chondropathy, synovitis and osteochondral pathology were each associated with OA at arthroplasty, but each was also identified in some 'non-arthritic' controls. Tidemark breaching in the chondropathy/osteophyte group was greater than in non-arthritic controls. Three histopathological subgroups were identified, characterised as 'mild OA', or 'severe OA' with mild or moderate/severe synovitis.

CONCLUSIONS

Presence and severity of synovitis helps define distinct histopathological OA subgroups. The absence of a discrete 'normal' subgroup indicates a pathological continuum between normality and OA status. Identifying specific pathological processes and their clinical correlates in OA subgroups has potential to accelerate the development of more effective therapies.

摘要

目的

骨关节炎(OA)是一种异质性多组织疾病。我们假设不同的组织病理学特征可表征膝关节OA进展的不同阶段,并且可以基于OA组织病理学特征的有效测量方法来定义不同的亚组。

设计

内侧胫骨平台和滑膜取自343例尸检(PM)和143例OA关节置换标本。“软骨病/骨赘”组(n = 217)被分类为有骨赘或宏观内侧胫股软骨病病变≥3级的PM病例,以代表手术前(早期)OA。从其余PM病例中确定“非关节炎”对照组(n = 48)。对Mankin组织病理学评分进行Rasch分析,并补充软骨下骨髓替代和滑膜炎的组织病理学评分。通过主成分分析(PCA)得出项目权重。使用潜在类别分析(LCA)寻找组织病理学亚组。

结果

软骨病、滑膜炎和骨软骨病理改变在关节置换时均与OA相关,但在一些“非关节炎”对照组中也有发现。软骨病/骨赘组的潮标突破大于非关节炎对照组。确定了三个组织病理学亚组,其特征为“轻度OA”或伴有轻度或中度/重度滑膜炎的“重度OA”。

结论

滑膜炎的存在和严重程度有助于定义不同的组织病理学OA亚组。不存在离散的“正常”亚组表明正常与OA状态之间存在病理连续性。确定OA亚组中的特定病理过程及其临床相关性有可能加速更有效治疗方法的开发。

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