Department of Clinical Pharmacology and Therapeutics, Asan Medical Center, Seoul, Korea.
University of Ulsan College of Medicine, Seoul, Korea.
J Clin Pharmacol. 2019 Apr;59(4):532-540. doi: 10.1002/jcph.1344. Epub 2018 Nov 19.
Amitriptyline is a tricyclic antidepressant that is metabolized mainly by CYP2C19 and CYP2D6 enzymes. Higher plasma levels of amitriptyline and its active metabolite, nortriptyline, are associated with an increased risk of adverse events including anticholinergic effects. The aim of this study was to evaluate the effects of CYP2C19 and CYP2D6 genetic polymorphisms on amitriptyline and nortriptyline pharmacokinetics. Twenty-four Korean healthy adult male volunteers were enrolled in the study after stratification by their CYP2C19 and CYP2D6 genotypes. Serial blood draws for pharmacokinetic analysis were made after a single oral 25-mg dose of amitriptyline was administered. Plasma amitriptyline and nortriptyline concentrations were measured by a validated liquid chromatography with tandem mass spectrometry. Population pharmacokinetic modeling analysis was conducted using NONMEM, which evaluated the effects of CYP2C19 and CYP2D6 genotypes on amitriptyline and nortriptyline pharmacokinetics. The biotransformation of amitriptyline into nortriptyline was significantly different between subjects with the CYP2C19*2/*2, *2/*3, and *3/3 genotypes and those with the other genotypes, with an estimated metabolic clearance of 17 and 61.5 L/h, respectively. Clearance of amitriptyline through pathways other than biotransformation into nortriptyline was estimated as 18.8 and 30.6 L/h for subjects with the CYP2D610/*10 and *10/*5 genotypes and those with the other genotypes, respectively. This study demonstrated a quantitative effect of the CYP2C19 and CYP2D6 genotypes on amitriptyline and nortriptyline pharmacokinetics. Production of nortriptyline from amitriptyline was associated with CYP2C19 genotypes, and clearance of amitriptyline through pathways other than biotransformation into nortriptyline was associated with CYP2D6 genotypes. These observations may be useful in developing individualized, optimal therapy with amitriptyline.
阿米替林是一种三环类抗抑郁药,主要通过 CYP2C19 和 CYP2D6 酶代谢。阿米替林和其活性代谢物去甲替林的血浆水平较高与不良反应风险增加相关,包括抗胆碱能作用。本研究旨在评估 CYP2C19 和 CYP2D6 基因多态性对阿米替林和去甲替林药代动力学的影响。24 名韩国健康成年男性志愿者在根据 CYP2C19 和 CYP2D6 基因型分层后被纳入研究。在单次口服 25mg 阿米替林后进行药代动力学分析的系列血样采集。采用液质联用方法测定血浆中阿米替林和去甲替林的浓度。采用 NONMEM 进行群体药代动力学模型分析,评估 CYP2C19 和 CYP2D6 基因型对阿米替林和去甲替林药代动力学的影响。阿米替林转化为去甲替林的生物转化在 CYP2C19*2/*2、*2/3 和3/3 基因型的受试者与其他基因型的受试者之间存在显著差异,估计代谢清除率分别为 17 和 61.5 L/h。通过除转化为去甲替林以外的途径清除阿米替林的估计值分别为 CYP2D610/10 和10/*5 基因型的受试者和其他基因型的受试者的 18.8 和 30.6 L/h。本研究表明 CYP2C19 和 CYP2D6 基因型对阿米替林和去甲替林药代动力学具有定量影响。阿米替林转化为去甲替林与 CYP2C19 基因型相关,而除转化为去甲替林以外的途径清除阿米替林与 CYP2D6 基因型相关。这些观察结果可能有助于开发个体化、最佳的阿米替林治疗方案。