Orthopaedics, Royal Liverpool and Broadgreen University Hospital, Liverpool , UK.
Expert Opin Investig Drugs. 2013 Apr;22(4):423-41. doi: 10.1517/13543784.2013.770837. Epub 2013 Feb 14.
Osteoarthritis is a disabling affliction, and disease-modifying osteoarthritis drugs (DMOADs) would be highly desirable adjuncts to symptomatic relief as they may delay the disease process.
This study is a comprehensive review of the recent literature on the efficacy of DMOADs in the treatment of OA. In vitro and in vivo evidence was collected using MEDLINE® (1950 to November 2012) and EMBASE (1980 to November 2012) databases. Several drugs have demonstrated DMOAD effects in OA. They can be divided into three groups based on their predominant mode of action: those targeting cartilage, inflammatory pathways and subchondral bone. OARSI guidelines recommend glucosamine and chondroitin sulphates and diacerein as DMOADS, and NICE will recommend glucosamine sulphate in the next update of guidelines. Exploration of improved outcome measures and identification of subgroups of patients most likely to benefit from different DMOADs are likely to be the most important areas of development over the coming years.
It is expected that a wider range of prospective clinical studies will be embarked upon in the coming years. Trials including MRI as well as joint space narrowing (JSN) should be designed in a systematic manner, powered with sufficient numbers to demonstrate clinical benefit at different stages of disease.
骨关节炎是一种使人丧失能力的疾病,作为缓解症状的辅助疗法,疾病修饰性骨关节炎药物(DMOADs)非常有吸引力,因为它们可能延缓疾病进程。
本研究对 DMOADs 治疗 OA 的近期文献进行了全面综述。使用 MEDLINE®(1950 年至 2012 年 11 月)和 EMBASE(1980 年至 2012 年 11 月)数据库收集了体外和体内证据。几种药物已证明对 OA 具有 DMOAD 作用。根据其主要作用模式,它们可分为三组:靶向软骨、炎症途径和软骨下骨的药物。OARSI 指南建议将氨基葡萄糖和硫酸软骨素以及双醋瑞因作为 DMOADs,NICE 将在指南的下一次更新中建议使用氨基葡萄糖硫酸盐。探索改善的疗效指标和确定最有可能从不同 DMOAD 中获益的患者亚组可能是未来几年最重要的发展领域。
预计未来几年将开展更广泛的前瞻性临床研究。应系统地设计包括 MRI 以及关节间隙变窄(JSN)的试验,并具有足够的数量,以在疾病的不同阶段证明临床获益。