Mengle-Gaw Laurel J, Schwartz Benjamin D
The Camden Group, 19 Oak Park Drive, St. Louis, MO 63141, USA.
Mediators Inflamm. 2002 Oct;11(5):275-86. doi: 10.1080/09629350290000041.
The discovery of two isoforms of the cyclooxygenase enzyme, COX-1 and COX-2, and the development of COX-2-specific inhibitors as anti-inflammatories and analgesics have offered great promise that the therapeutic benefits of NSAIDs could be optimized through inhibition of COX-2, while minimizing their adverse side effect profile associated with inhibition of COX-1. While COX-2 specific inhibitors have proven to be efficacious in a variety of inflammatory conditions, exposure of large numbers of patients to these drugs in postmarketing studies have uncovered potential safety concerns that raise questions about the benefit/risk ratio of COX-2-specific NSAIDs compared to conventional NSAIDs. This article reviews the efficacy and safety profiles of COX-2-specific inhibitors, comparing them with conventional NSDAIDs.
环氧化酶(COX)两种同工型COX-1和COX-2的发现,以及作为抗炎药和镇痛药的COX-2特异性抑制剂的研发,带来了巨大的希望,即通过抑制COX-2可以优化非甾体抗炎药(NSAIDs)的治疗益处,同时将与抑制COX-1相关的不良副作用降至最低。虽然COX-2特异性抑制剂已被证明在多种炎症性疾病中有效,但在上市后研究中大量患者使用这些药物后发现了潜在的安全问题,这引发了关于COX-2特异性NSAIDs与传统NSAIDs相比的效益/风险比的疑问。本文综述了COX-2特异性抑制剂的疗效和安全性,并将它们与传统NSAIDs进行比较。