Ryu S, Park S, Lee J H, Kim Y R, Na H S, Lim H S, Choi H Y, Hwang I Y, Lee J G, Park Z W, Oh W Y, Kim J M, Choi S E
Clinical Research Division, National Institute of Food and Drug Safety, Ministry of Food and Drug Safety, Republic of Korea.
Department of Clinical Pharmacology and Therapeutics, College of Medicine, University of Ulsan, Asan Medical Center, Republic of Korea.
Clin Transl Sci. 2017 Mar;10(2):93-101. doi: 10.1111/cts.12451. Epub 2017 Mar 14.
We performed a double-blinded, genotype-based stratification study to explore the pharmacokinetics and pharmacodynamics of amitriptyline according to CYP2C19 and CYP2D6 genotype in Korean subjects. Twenty-four healthy adults were grouped by genotype of CYP2C19 and CYP2D6. After a single dose of 25 mg of amitriptyline, blood samples were collected and anticholinergic effects were measured. The extent of N-demethylation of amitriptyline significantly decreased in subjects carrying two nonfunctional alleles of CYP2C19. The extent of hydroxylation of amitriptyline or nortriptyline was significantly reduced in subjects carrying two CYP2D6 decreased functional alleles compared with those with no or one decreased functional allele. The overall metabolic pathway of amitriptyline was more likely to be dominated by CYP2C19 than CYP2D6. The gene variations of CYP2C19 and CYP2D6 did not change the pharmacodynamic effect. The findings of this study will provide useful information on individualized drug treatment with amitriptyline considering both CYP2D6 and CYP2C19 gene variations.
我们进行了一项双盲、基于基因型分层的研究,以探讨在韩国受试者中,根据CYP2C19和CYP2D6基因型,阿米替林的药代动力学和药效学情况。24名健康成年人按CYP2C19和CYP2D6基因型分组。单次服用25毫克阿米替林后,采集血样并测量抗胆碱能效应。携带两个CYP2C19无功能等位基因的受试者中,阿米替林的N-去甲基化程度显著降低。与携带零个或一个功能降低等位基因的受试者相比,携带两个CYP2D6功能降低等位基因的受试者中,阿米替林或去甲替林的羟基化程度显著降低。阿米替林的总体代谢途径更可能由CYP2C19而非CYP2D6主导。CYP2C19和CYP2D6的基因变异并未改变药效学效应。本研究结果将为考虑CYP2D6和CYP2C19基因变异的阿米替林个体化药物治疗提供有用信息。