Gaedigk Andrea, Dinh Jean C, Jeong Hyunyoung, Prasad Bhagwat, Leeder J Steven
Division of Clinical Pharmacology, Toxicology & Therapeutic Innovation, Children's Mercy Kansas City, 2401 Gillham Rd, Kanas City, MO 64108, USA.
School of Medicine, University of Missouri-Kansas City, Kansas City, MO 64108, USA.
J Pers Med. 2018 Apr 17;8(2):15. doi: 10.3390/jpm8020015.
The seminal paper on the CYP2D6 Activity Score (AS) was first published ten years ago and, since its introduction in 2008, it has been widely accepted in the field of pharmacogenetics. This scoring system facilitates the translation of highly complex diplotype data into a patient’s phenotype to guide drug therapy and is at the core of all gene/drug pair guidelines issued by the Clinical Pharmacogenetics Implementation Consortium (CPIC). The AS, however, only explains a portion of the variability observed among individuals and ethnicities. In this review, we provide an overview of sources in addition to genotype that contribute to the variability in CYP2D6-mediated drug metabolism and discuss other factors, genetic and non-genetic, that likely contribute to the observed variability in CYP2D6 enzymatic activity.
关于CYP2D6活性评分(AS)的开创性论文于十年前首次发表,自2008年引入以来,它在药物遗传学领域已被广泛接受。这种评分系统有助于将高度复杂的双倍型数据转化为患者的表型,以指导药物治疗,并且是临床药物遗传学实施联盟(CPIC)发布的所有基因/药物对指南的核心。然而,AS仅解释了个体和种族间观察到的部分变异性。在本综述中,我们除了概述导致CYP2D6介导的药物代谢变异性的基因型来源外,还讨论了其他可能导致观察到的CYP2D6酶活性变异性的遗传和非遗传因素。