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临床药物遗传学实施联盟指南:CYP2D6、OPRM1 和 COMT 基因型与选择性阿片类药物治疗。

Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2D6, OPRM1, and COMT Genotypes and Select Opioid Therapy.

机构信息

Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

Department of Emergency Medicine & Colorado Center for Personalized Medicine, University of Colorado School of Medicine, Aurora, Colorado, USA.

出版信息

Clin Pharmacol Ther. 2021 Oct;110(4):888-896. doi: 10.1002/cpt.2149. Epub 2021 Feb 9.

Abstract

Opioids are mainly used to treat both acute and chronic pain. Several opioids are metabolized to some extent by CYP2D6 (codeine, tramadol, hydrocodone, oxycodone, and methadone). Polymorphisms in CYP2D6 have been studied for an association with the clinical effect and safety of these drugs. Other genes that have been studied for their association with opioid clinical effect or adverse events include OPRM1 (mu receptor) and COMT (catechol-O-methyltransferase). This guideline updates and expands the 2014 Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline for CYP2D6 genotype and codeine therapy and includes a summation of the evidence describing the impact of CYP2D6, OPRM1, and COMT on opioid analgesia and adverse events. We provide therapeutic recommendations for the use of CYP2D6 genotype results for prescribing codeine and tramadol and describe the limited and/or weak data for CYP2D6 and hydrocodone, oxycodone, and methadone, and for OPRM1 and COMT for clinical use.

摘要

阿片类药物主要用于治疗急性和慢性疼痛。几种阿片类药物在一定程度上通过 CYP2D6(可待因、曲马多、氢可酮、羟考酮和美沙酮)代谢。已经研究了 CYP2D6 的多态性与这些药物的临床疗效和安全性的关联。其他与阿片类药物临床疗效或不良反应相关的基因包括 OPRM1(mu 受体)和 COMT(儿茶酚-O-甲基转移酶)。本指南更新并扩展了 2014 年临床药物遗传学实施联盟 (CPIC) 关于 CYP2D6 基因型和可待因治疗的指南,并总结了描述 CYP2D6、OPRM1 和 COMT 对阿片类镇痛药和不良反应影响的证据。我们为使用 CYP2D6 基因型结果开处方可待因和曲马多提供治疗建议,并描述了 CYP2D6 和氢可酮、羟考酮和美沙酮以及 OPRM1 和 COMT 用于临床的有限和/或弱数据。

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