Rheumatology Department, Hospital Universitario Virgen Macarena, Avda Doctor Fedriani 3, 41011 Sevilla, Spain.
Ann Rheum Dis. 2011 Nov;70(11):1957-62. doi: 10.1136/ard.2011.152017. Epub 2011 Aug 17.
AMELIA (OsteoArthritis Modifying Effects of Long-term Intra-articular Adant) was designed to compare against placebo the efficacy and safety of repeated injections of hyaluronic acid (HA) and its effect on disease progression over 40 months.
A multicentre, randomised, patient and evaluator-blinded, controlled study in 306 patients fulfilling American College of Rheumatology criteria for knee osteoarthritis, radiological grades II-III (Kellgren-Lawrence) and joint space width ≥ 2 mm. Patients received four cycles of five intra-articular HA or placebo injections with a follow-up of 6 months after the first and second cycles, and 1 year after the third and fourth cycles. Osteoarthritis Research Society International (OARSI) 2004 responder criteria were used to assess efficacy. The consumption of rescue medication was a secondary outcome. Adverse events were recorded for safety purposes.
At the 40-month visit significantly more patients responded to HA compared with placebo (OARSI 2004, p=0.004). The number of responders to HA increased through the study, whereas those to placebo did not change. Significant differences were also found in favour of HA for each individual component of the OARSI 2004. No safety problems were recorded.
The results of AMELIA offer pioneer evidence that repeated cycles of intra-articular injections of HA not only improve knee osteoarthritis symptoms during the in-between cycle period but also exert a marked carry-over effect for at least 1 year after the last cycle. In this respect, it is not possible to establish if this carry-over effect reflects true osteoarthritis remission or just a modification of the disease's natural course. ClinicalTrials.gov number, NCT00669032.
AMELIA(骨关节炎长期关节内阿达特的矫形效果)旨在比较透明质酸(HA)重复关节内注射的疗效和安全性以及对 40 个月疾病进展的影响。
这是一项多中心、随机、患者和评估者双盲、对照研究,纳入了 306 名符合美国风湿病学会膝关节骨关节炎标准、影像学分级 II-III(Kellgren-Lawrence)和关节间隙宽度≥2mm 的患者。患者接受 4 个周期的 5 次关节内 HA 或安慰剂注射,在第一和第二周期后进行 6 个月随访,在第三和第四周期后进行 1 年随访。采用骨关节炎研究协会国际(OARSI)2004 年应答标准评估疗效。使用挽救药物的消耗作为次要终点。记录不良事件以评估安全性。
在 40 个月的随访中,接受 HA 治疗的患者与安慰剂组相比,应答者明显更多(OARSI 2004,p=0.004)。接受 HA 治疗的患者应答者数量在研究过程中增加,而接受安慰剂治疗的患者则没有变化。HA 组在 OARSI 2004 的每个单项指标上也表现出显著优势。未发现安全性问题。
AMELIA 的结果提供了开创性的证据,表明重复关节内注射 HA 不仅可以改善关节内注射期间膝关节骨关节炎的症状,而且在最后一个周期后至少 1 年内还具有明显的持续作用。在这方面,无法确定这种持续作用是否反映了真正的骨关节炎缓解,还是仅仅是对疾病自然病程的一种修饰。临床试验编号,NCT00669032。