Institute for Translational Medicine and Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Division of Pharmacotherapy and Experimental Therapeutics, Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina, USA.
Clin Pharmacol Ther. 2020 Aug;108(2):191-200. doi: 10.1002/cpt.1830. Epub 2020 Apr 28.
Nonsteroidal anti-inflammatory drugs (NSAIDs) are among the most commonly used analgesics due to their lack of addictive potential. However, NSAIDs have the potential to cause serious gastrointestinal, renal, and cardiovascular adverse events. CYP2C9 polymorphisms influence metabolism and clearance of several drugs in this class, thereby affecting drug exposure and potentially safety. We summarize evidence from the published literature supporting these associations and provide therapeutic recommendations for NSAIDs based on CYP2C9 genotype (updates at www.cpicpgx.org).
非甾体抗炎药(NSAIDs)由于缺乏成瘾性而成为最常用的镇痛药之一。然而,NSAIDs 有可能引起严重的胃肠道、肾脏和心血管不良事件。CYP2C9 多态性影响该类药物的代谢和清除,从而影响药物暴露和潜在的安全性。我们总结了来自已发表文献的证据,支持这些关联,并根据 CYP2C9 基因型为 NSAIDs 提供治疗建议(www.cpicpgx.org 更新)。