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骨关节炎是一种异质性疾病,可以分为亚组吗?

Is osteoarthritis a heterogeneous disease that can be stratified into subsets?

机构信息

Department of Kinesiology, Temple University, 002 Pearson Hall, 1800 N. Broad Street, Philadelphia, PA 19122, USA.

出版信息

Clin Rheumatol. 2010 Feb;29(2):123-31. doi: 10.1007/s10067-009-1301-1. Epub 2009 Nov 19.

DOI:10.1007/s10067-009-1301-1
PMID:19924499
Abstract

Osteoarthritis is a heterogeneous disease characterized by variable clinical features, biochemical/genetic characteristics, and responses to treatments. To optimize palliative effects of current treatments and develop efficacious disease-modifying interventions, treatments may need to be tailored to the individual or a subset of osteoarthritic joints. The purpose of this review is to explore the current literature on the clinical and physiological variability in osteoarthritis and potential for stratifying patients. Several stratifications have been reported, including mechanism of onset, stage of disease progression, involved joints, inflammatory levels, and effusion. Most of these methods revealed two to three unique subsets of osteoarthritis. Osteoarthritic joints may be stratified by an array of variables, some transient and others consistent throughout the disease process. Future research needs to continue to explore stratification techniques since these may be the key to optimizing palliative interventions and developing disease-modifying interventions for subsets within this heterogeneous disease.

摘要

骨关节炎是一种异质性疾病,其临床特征、生化/遗传特征和对治疗的反应各不相同。为了优化现有治疗的姑息效果并开发有效的疾病修饰干预措施,可能需要根据个体或亚组的骨关节炎关节来调整治疗方法。本文旨在探讨骨关节炎的临床和生理变异性以及分层患者的潜力的现有文献。已经报道了几种分层方法,包括发病机制、疾病进展阶段、受累关节、炎症水平和渗出液。这些方法中的大多数揭示了骨关节炎的两个到三个独特亚组。可以通过一系列变量对骨关节炎关节进行分层,其中一些是短暂的,而另一些则在整个疾病过程中保持不变。未来的研究需要继续探索分层技术,因为这些技术可能是优化姑息干预措施和开发针对这种异质性疾病亚组的疾病修饰干预措施的关键。

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Long-Acting Extracellular Vesicle-Based Biologics in Osteoarthritis Immunotherapy.用于骨关节炎免疫治疗的长效细胞外囊泡生物制剂
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本文引用的文献

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Association between interleukin 1 gene cluster polymorphisms and bilateral distal interphalangeal osteoarthritis.白细胞介素1基因簇多态性与双侧远端指间关节骨关节炎之间的关联。
J Rheumatol. 2009 Sep;36(9):1977-86. doi: 10.3899/jrheum.081238. Epub 2009 Aug 14.
2
Identification of progressors in osteoarthritis by combining biochemical and MRI-based markers.通过结合生化指标和基于磁共振成像的指标来识别骨关节炎的进展者
Arthritis Res Ther. 2009;11(4):R115. doi: 10.1186/ar2774. Epub 2009 Jul 24.
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Primary osteoarthritis no longer primary: three subsets with distinct etiological, clinical, and therapeutic characteristics.
对批量和单细胞RNA测序数据的综合分析揭示了骨关节炎软骨细胞中花生四烯酸代谢增加。
Front Med (Lausanne). 2025 May 9;12:1552029. doi: 10.3389/fmed.2025.1552029. eCollection 2025.
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Multifaceted imaging strategies for clinical trials of knee osteoarthritis-a tightly interlinked value and precision chain.膝关节骨关节炎临床试验的多维度成像策略——一个紧密相连的价值与精准链条。
Skeletal Radiol. 2025 Apr 1. doi: 10.1007/s00256-025-04919-0.
5
Development of methodology to support molecular endotype discovery from synovial fluid of individuals with knee osteoarthritis: The STEpUP OA consortium.从膝骨关节炎患者的滑液中开发支持分子内表型发现的方法学: STEpUPOA 联盟。
PLoS One. 2024 Nov 18;19(11):e0309677. doi: 10.1371/journal.pone.0309677. eCollection 2024.
6
Phenotypes of osteoarthritis-related knee pain and their transition over time: data from the osteoarthritis initiative.骨关节炎相关膝关节疼痛的表型及其随时间的变化:来自骨关节炎倡议的数据。
BMC Musculoskelet Disord. 2024 Feb 24;25(1):173. doi: 10.1186/s12891-024-07286-4.
7
"You don't put it down to arthritis": A qualitative study of the first symptoms recalled by individuals with knee osteoarthritis.“你不会将其归因于关节炎”:一项关于膝骨关节炎患者回忆的首发症状的定性研究。
Osteoarthr Cartil Open. 2023 Dec 16;6(1):100428. doi: 10.1016/j.ocarto.2023.100428. eCollection 2024 Mar.
8
Identifying multivariate disease trajectories and potential phenotypes of early knee osteoarthritis in the CHECK cohort.在 CHECK 队列中识别早期膝骨关节炎的多变量疾病轨迹和潜在表型。
PLoS One. 2023 Jul 14;18(7):e0283717. doi: 10.1371/journal.pone.0283717. eCollection 2023.
9
Early pain in females is linked to late pathological features in murine experimental osteoarthritis.女性早期疼痛与小鼠实验性骨关节炎后期的病理特征有关。
PeerJ. 2023 Jun 22;11:e15482. doi: 10.7717/peerj.15482. eCollection 2023.
10
Mesenchymal progenitor cells from non-inflamed versus inflamed synovium post-ACL injury present with distinct phenotypes and cartilage regeneration capacity.非炎症性与炎症性 ACL 损伤后滑膜间充质祖细胞表现出不同的表型和软骨再生能力。
Stem Cell Res Ther. 2023 Jun 25;14(1):168. doi: 10.1186/s13287-023-03396-3.
原发性骨关节炎不再“原发”:具有不同病因、临床和治疗特征的三个亚组。
Semin Arthritis Rheum. 2009 Oct;39(2):71-80. doi: 10.1016/j.semarthrit.2009.03.006. Epub 2009 Jul 9.
4
Relationship of compartment-specific structural knee status at baseline with change in cartilage morphology: a prospective observational study using data from the osteoarthritis initiative.基线时特定腔室结构膝关节状态与软骨形态变化的关系:一项使用来自骨关节炎倡议的数据的前瞻性观察研究。
Arthritis Res Ther. 2009;11(3):R90. doi: 10.1186/ar2732. Epub 2009 Jun 17.
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Local cytokine profiles in knee osteoarthritis: elevated synovial fluid interleukin-15 differentiates early from end-stage disease.膝关节骨关节炎的局部细胞因子谱:升高的滑液白细胞介素-15 可将早期与终末期疾病区分开来。
Osteoarthritis Cartilage. 2009 Aug;17(8):1040-8. doi: 10.1016/j.joca.2009.02.011. Epub 2009 Mar 6.
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Confirmation of two major polyarticular osteoarthritis (POA) phenotypes--differentiation on the basis of joint topography.两种主要的多关节型骨关节炎(POA)表型的确认——基于关节部位的区分。
Osteoarthritis Cartilage. 2009 Jul;17(7):891-5. doi: 10.1016/j.joca.2009.01.003. Epub 2009 Jan 21.
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Correlation of plasma and synovial fluid osteopontin with disease severity in knee osteoarthritis.血浆和滑液骨桥蛋白与膝关节骨关节炎疾病严重程度的相关性
Clin Biochem. 2009 Jun;42(9):808-12. doi: 10.1016/j.clinbiochem.2009.02.002. Epub 2009 Feb 13.
8
Inflammatory response in patients with active and inactive osteoarthritis.活动期和非活动期骨关节炎患者的炎症反应。
Rheumatol Int. 2009 Aug;29(10):1197-203. doi: 10.1007/s00296-009-0864-0. Epub 2009 Jan 30.
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The genetic influence on radiographic osteoarthritis is site specific at the hand, hip and knee.基因对手部、髋部和膝部的影像学骨关节炎的影响具有部位特异性。
Rheumatology (Oxford). 2009 Mar;48(3):277-80. doi: 10.1093/rheumatology/ken475. Epub 2009 Jan 19.
10
Quadriceps strength and the risk of cartilage loss and symptom progression in knee osteoarthritis.股四头肌力量与膝关节骨关节炎软骨损伤及症状进展风险
Arthritis Rheum. 2009 Jan;60(1):189-98. doi: 10.1002/art.24182.