Impact of CYP2D6, CYP3A5, and ABCB1 Polymorphisms on Plasma Concentrations of Donepezil and Its Metabolite in Patients With Alzheimer Disease
- PMID: 33065613
- DOI: 10.1097/FTD.0000000000000823
Impact of CYP2D6, CYP3A5, and ABCB1 Polymorphisms on Plasma Concentrations of Donepezil and Its Metabolite in Patients With Alzheimer Disease
Abstract
Background: Donepezil is one of the most commonly prescribed drugs for the treatment of Alzheimer disease. It is predominantly metabolized through CYP2D6 and to a lesser extent by CYP3A4/5. There are conflicting reports regarding the influence of CYP2D6, CYP3A5, and ABCB1 polymorphisms on the plasma concentration of donepezil. This study investigated the influence of these polymorphisms and sex on the plasma concentrations of donepezil and its active metabolite, 6-O-desmethyl donepezil (6ODD), in 47 patients with Alzheimer disease.
Methods: Plasma donepezil and 6ODD concentrations were measured using liquid chromatography tandem mass spectrometry. Sex, the concomitant use of psychotropics, and CYP2D6, CYP3A5, and ABCB1 polymorphisms were analyzed as possible influencers.
Results: The mean plasma concentrations of donepezil and 6ODD were well correlated (R2 = 0.418). The mean plasma concentration ratio of donepezil to 6ODD (metabolic ratio) was significantly lower in intermediate metabolizers of CYP2D6 than in extensive metabolizers. The metabolic ratio in patients receiving psychotropics was significantly lower than in those not receiving psychotropics. Among intermediate metabolizers, patients positive for CYP3A5 *3/*3 showed a significant increase in plasma mean 6ODD concentrations when compared with those who did not express this gene (CYP3A5 *1/*1 or *1/*3).
Conclusions: Results indicate that the mean plasma concentration ratio of donepezil to 6ODD is associated with CYP2D6 polymorphism and the concomitant use of psychotropics in patients with Alzheimer disease. In intermediate metabolizers, CYP3A5 may play a significant role in the metabolism of donepezil.
Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved.
Conflict of interest statement
The authors declare no conflict of interest.
Similar articles
-
Influence of CYP2D6, CYP3A4, CYP3A5 and ABCB1 Polymorphisms on Pharmacokinetics and Safety of Aripiprazole in Healthy Volunteers.Basic Clin Pharmacol Toxicol. 2018 Jun;122(6):596-605. doi: 10.1111/bcpt.12960. Epub 2018 Feb 22. Basic Clin Pharmacol Toxicol. 2018. PMID: 29325225
-
Effects of genetic polymorphisms of CYP2D6, CYP3A5, and ABCB1 on the steady-state plasma concentrations of aripiprazole and its active metabolite, dehydroaripiprazole, in Japanese patients with schizophrenia.Ther Drug Monit. 2014 Oct;36(5):651-5. doi: 10.1097/FTD.0000000000000070. Ther Drug Monit. 2014. PMID: 24682161
-
Do CYP3A and ABCB1 genotypes influence the plasma concentration and clinical outcome of donepezil treatment?Eur J Clin Pharmacol. 2011 Jan;67(1):47-54. doi: 10.1007/s00228-010-0883-5. Epub 2010 Oct 8. Eur J Clin Pharmacol. 2011. PMID: 20931330
-
Effect of CYP3A and ABCB1 single nucleotide polymorphisms on the pharmacokinetics and pharmacodynamics of calcineurin inhibitors: Part I.Clin Pharmacokinet. 2010 Mar;49(3):141-75. doi: 10.2165/11317350-000000000-00000. Clin Pharmacokinet. 2010. PMID: 20170205 Review.
-
Pharmacogenetic aspects of therapy with cholinesterase inhibitors: the role of CYP2D6 in Alzheimer's disease pharmacogenetics.Curr Alzheimer Res. 2007 Sep;4(4):479-500. doi: 10.2174/156720507781788846. Curr Alzheimer Res. 2007. PMID: 17908053 Review.
Cited by
-
Revisiting the Metabolism of Donepezil in Rats Using Non-Targeted Metabolomics and Molecular Networking.Pharmaceutics. 2025 Jan 15;17(1):115. doi: 10.3390/pharmaceutics17010115. Pharmaceutics. 2025. PMID: 39861762 Free PMC article.
-
Pharmacogenetics of Donepezil and Memantine in Healthy Subjects.J Pers Med. 2022 May 13;12(5):788. doi: 10.3390/jpm12050788. J Pers Med. 2022. PMID: 35629210 Free PMC article.
-
Impact of Plasma Donepezil Concentration on Behavioral and Psychological Symptoms of Dementia in Patients with Alzheimer's Disease.Dement Geriatr Cogn Dis Extra. 2021 Dec 2;11(3):264-272. doi: 10.1159/000516938. eCollection 2021 Sep-Dec. Dement Geriatr Cogn Dis Extra. 2021. PMID: 35082823 Free PMC article.
-
The impact of CYP2D6 on donepezil concentration and its lack of effect on the treatment response and adverse effect in Korean patients with Alzheimer's disease.Korean J Physiol Pharmacol. 2025 Mar 1;29(2):227-233. doi: 10.4196/kjpp.24.239. Epub 2024 Nov 14. Korean J Physiol Pharmacol. 2025. PMID: 39539179 Free PMC article.
-
Pregnancy Increases CYP3A Enzymes Activity as Measured by the 4β-Hydroxycholesterol/Cholesterol Ratio.Int J Mol Sci. 2022 Dec 2;23(23):15168. doi: 10.3390/ijms232315168. Int J Mol Sci. 2022. PMID: 36499500 Free PMC article.
References
-
- Alzheimer's Association. 2016 Alzheimer's disease facts and figures. Alzheimers Dement. 2016;12:459–509.
-
- Barner EL, Gray SL. Donepezil use in Alzheimer disease. Ann Pharmacother. 1998;32:70–77.
-
- Coin A, Pamio MV, Alexopoulos C, et al. Donepezil plasma concentrations, CYP2D6 and CYP3A4 phenotypes, and cognitive outcome in Alzheimer's disease. Eur J Clin Pharmacol. 2016;72:711–717.
-
- Matsui K, Mishima M, Nagai Y, et al. Absorption, distribution, metabolism, and excretion of donepezil (aricept) after a single oral administration to rat. Drug Metab Dispos. 1999;27:1406–1414.
-
- Magliulo L, Dahl ML, Lombardi G, et al. Do CYP3A and ABCB1 genotypes influence the plasma concentration and clinical outcome of donepezil treatment? Eur J Clin Pharmacol. 2011;67:47–54.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical