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环氧化酶抑制:疼痛、炎症与心血管系统。

Cyclooxygenase Inhibition: Pain, Inflammation, and the Cardiovascular System.

机构信息

Institute for Translational Medicine and Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

出版信息

Clin Pharmacol Ther. 2017 Oct;102(4):611-622. doi: 10.1002/cpt.794. Epub 2017 Aug 17.

Abstract

Inhibitors of the cyclooxygenases (COXs), the nonsteroidal antiinflammatory drugs (NSAIDs), relieve inflammatory pain, but are associated with gastrointestinal and cardiovascular complications. Given the widespread use of NSAIDs, there has been a longstanding interest in optimizing their risk-benefit ratio, for example by reducing their gastrointestinal risk. More recently, the focus has shifted toward the cardiovascular complications of NSAIDs and very large prospective studies have been performed to compare cardiovascular risk across distinct NSAIDs. Surprisingly, much less attention has been paid to the efficacy side of the risk-benefit ratio. There is marked variability in the degree of pain relief by NSAIDs due to the complex interplay of molecular mechanisms contributing to the pain sensation, variability in the disposition of NSAIDs, and imprecision in the quantification of human pain. Here we discuss how NSAIDs relieve pain, how molecular mechanisms relate to clinical efficacy, and how this may inform our interpretation of clinical trials.

摘要

环氧化酶 (COX) 抑制剂,即非甾体类抗炎药 (NSAIDs),可以缓解炎症性疼痛,但与胃肠道和心血管并发症相关。鉴于 NSAIDs 的广泛应用,人们长期以来一直致力于优化其风险效益比,例如降低胃肠道风险。最近,人们的关注点转向了 NSAIDs 的心血管并发症,并且进行了非常大型的前瞻性研究来比较不同 NSAIDs 的心血管风险。令人惊讶的是,对于风险效益比的疗效方面,关注得要少得多。由于导致疼痛感觉的分子机制的复杂相互作用、NSAIDs 处置的变异性以及人类疼痛量化的不精确性,NSAIDs 的止痛效果存在明显差异。在这里,我们讨论 NSAIDs 如何缓解疼痛,分子机制如何与临床疗效相关,以及这如何帮助我们解释临床试验。

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