Division of Musculoskeletal Disease, Leeds Institute of Molecular Medicine, University of Leeds, UK.
Rheumatology (Oxford). 2013 May;52(5):888-92. doi: 10.1093/rheumatology/kes386. Epub 2013 Jan 7.
Synovitis is very common in knee OA and associated with pain. This open-label study evaluated an anti-synovitis therapy, MTX, for pain relief in knee OA.
Inclusion criteria included pain visual analogue scale (VAS) >40/100 mm, ACR clinical criteria for knee OA and intolerance/inefficacy of NSAID and opioids. US at baseline and 24 weeks assessed effusion and synovial thickness. Patients received MTX up to 20 mg/week for 24 weeks.
Thirty participants were recruited; mean age 64.5 years, median pain VAS 68 mm. At 24 weeks, 13/30 (43%) achieved ≥30% reduction in pain VAS, 7 (23%) achieved ≥50% reduction and 4 (13%) had worsened. Thirteen achieved Osteoarthritis Research Society International (OARSI) responder criteria. All had effusion/synovitis at baseline. There was no correlation between change in imaging and change in pain scores at 24 weeks.
This open-label trial suggests analgesic efficacy for MTX in OA knee and suggests that a randomized controlled trial is warranted. Trial Registration. Current controlled trials, http://www.controlled-trials.com/, ISRCTN66676866.
关节炎性滑膜炎在膝骨关节炎中非常常见,并与疼痛有关。本开放性研究评估了一种抗关节炎滑膜药物(MTX)治疗膝骨关节炎疼痛的疗效。
纳入标准包括疼痛视觉模拟评分(VAS)>40/100mm、美国风湿病学会(ACR)膝骨关节炎临床标准以及非甾体抗炎药和阿片类药物不耐受/无效。基线和 24 周时进行超声检查,评估关节积液和滑膜厚度。患者接受 MTX 治疗,剂量为每周 20mg,共 24 周。
共招募了 30 名参与者,平均年龄 64.5 岁,中位疼痛 VAS 为 68mm。24 周时,13/30(43%)名患者疼痛 VAS 降低≥30%,7 名(23%)患者降低≥50%,4 名(13%)患者疼痛加重。13 名患者达到骨关节炎研究协会国际(OARSI)的应答标准。所有患者基线时均存在关节积液/滑膜炎。24 周时影像学变化与疼痛评分变化之间无相关性。
本开放性试验表明 MTX 对膝骨关节炎具有镇痛疗效,提示有必要进行随机对照试验。试验注册。当前对照试验,http://www.controlled-trials.com/,ISRCTN66676866。