Steinmeyer Jürgen, Konttinen Yrjö T
Clinic and Policlinic of Orthopaedics and Orthopaedic Surgery, University Hospital Giessen and Marburg GmbH, Paul-Meimberg-Strasse 3, D-35385 Giessen, Germany.
Adv Drug Deliv Rev. 2006 May 20;58(2):168-211. doi: 10.1016/j.addr.2006.01.007. Epub 2006 Apr 17.
Alleviation of pain and inhibition of inflammation are the primary goals of pharmacotherapy of osteoarthritis (OA). These therapeutic goals can almost always be accomplished by the use of analgesics and nonsteroidal anti-inflammatory drugs (NSAID). One of the main problems of NSAIDs is their gastrointestinal toxicity, for which a prophylactic medication should be considered particularly amongst risk groups. Recent studies have shown that COX-2-selective and maybe also non-selective NSAIDs increase the cardiovascular risk so that their application is getting now drastically restricted. Pharmacological results published until now suggest that a clinically relevant minor analgesic and/or anti-inflammatory effect can be attained with the use of some of the SYmptomatic Slow Acting Drugs in OA (SYSADOAs). However, no clinical studies exist, which can positively confirm prevention, slowing down or reversal of any advanced joint cartilage destruction by any individual medication. Disease modifying therapy is still in its infancy; discovery and development of novel therapeutic targets and agents are an extremely difficult task, currently challenging many pharmaceutical companies and academic institutions.
减轻疼痛和抑制炎症是骨关节炎(OA)药物治疗的主要目标。这些治疗目标几乎总能通过使用镇痛药和非甾体抗炎药(NSAID)来实现。NSAIDs的主要问题之一是其胃肠道毒性,对于高危人群尤其应考虑预防性用药。最近的研究表明,COX-2选择性NSAIDs以及可能的非选择性NSAIDs会增加心血管风险,因此它们的应用目前受到极大限制。迄今为止发表的药理学研究结果表明,使用某些骨关节炎症状性缓解慢作用药物(SYSADOAs)可获得具有临床意义的轻微镇痛和/或抗炎效果。然而,尚无临床研究能够确切证实任何单一药物可预防、减缓或逆转晚期关节软骨破坏。疾病改善疗法仍处于起步阶段;发现和开发新的治疗靶点及药物是一项极其艰巨的任务,目前正挑战着许多制药公司和学术机构。