Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, 230032, Anhui, China.
Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, 7000, Australia.
Clin Rheumatol. 2024 Aug;43(8):2417-2433. doi: 10.1007/s10067-024-07042-y. Epub 2024 Jul 3.
The burden of osteoarthritis (OA) is rapidly increasing with population aging, but there are still no approved disease-modifying drugs available. Accumulating evidence has shown that OA is a heterogeneous disease with multiple phenotypes, and it is unlikely to respond to one-size-fits-all treatments. Inflammation is recognized as an important phenotype of OA and is associated with worse pain and joint deterioration. Therefore, it is believed that anti-inflammatory treatments may be more effective for OA with an inflammatory phenotype. In this review, we summarized clinical trials that evaluated anti-inflammatory treatments for OA and discussed whether these treatments are more effective in inflammatory OA phenotypes compared to general OA patients.
骨关节炎(OA)的负担随着人口老龄化迅速增加,但仍没有批准的疾病修饰药物可用。越来越多的证据表明,OA 是一种具有多种表型的异质性疾病,不太可能对一刀切的治疗方法产生反应。炎症被认为是 OA 的一个重要表型,与更严重的疼痛和关节恶化有关。因此,人们认为抗炎治疗可能对具有炎症表型的 OA 更有效。在这篇综述中,我们总结了评估 OA 抗炎治疗的临床试验,并讨论了这些治疗方法在炎症性 OA 表型与普通 OA 患者相比是否更有效。
Rheumatology (Oxford). 2017-6-1
Nat Rev Rheumatol. 2018-11
Expert Opin Emerg Drugs. 2018-12-3
Biochem Pharmacol. 2019-3-1
Immunopharmacol Immunotoxicol. 2019-7-11
Age Ageing. 2013-4-8
Extracell Vesicles Circ Nucl Acids. 2025-4-29
Front Bioeng Biotechnol. 2025-8-6
JAMA. 2023-10-24
Arthritis Care Res (Hoboken). 2023-9