Ovejero-Benito María C, Ochoa Dolores, Enrique-Benedito Teresa, Del Peso-Casado Miriam, Zubiaur Pablo, Navares Marcos, Román Manuel, Abad-Santos Francisco
Clinical Pharmacology Department, Instituto de Investigación Sanitaria La Princesa (IP), Hospital Universitario de La Princesa, 28006 Madrid, Spain.
Faculty of Medicine, Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain.
J Pers Med. 2022 May 13;12(5):788. doi: 10.3390/jpm12050788.
Donepezil and memantine are the most common drugs used for Alzheimer's disease. Their low effectiveness could partly be explained by genetic factors. Thus, we aim to identify Single Nucleotide Polymorphisms (SNPs) associated with pharmacokinetics, pharmacodynamics, and the safety of donepezil and memantine. For this regard, 25 volunteers enrolled in a bioequivalence clinical trial were genotyped for 67 SNPs in 21 genes with a ThermoFisher QuantStudio 12K Flex OpenArray. The statistical strategy included a univariate analysis that analyzed the association of these SNPs with pharmacokinetic parameters or the development of adverse drug reactions (ADRs) followed by a Bonferroni-corrected multivariate regression. Statistical analyses were performed with SPSS software v.21 and R commander (version v3.6.3). In the univariate analysis, fourteen and sixteen SNPs showed a significant association with memantine's and donepezil's pharmacokinetic parameters, respectively. Rs20417 () was associated with the development of at least one ADR. However, none of these associations reached the significance threshold in the Bonferroni-corrected multivariate analysis. In conclusion, we did not observe any significant association of the SNPs analyzed with memantine and donepezil pharmacokinetics or ADRs. Current evidence on memantine and donepezil pharmacogenetics does not justify their inclusion in pharmacogenetic guidelines.
多奈哌齐和美金刚是治疗阿尔茨海默病最常用的药物。它们疗效欠佳的部分原因可能是遗传因素。因此,我们旨在确定与多奈哌齐和美金刚的药代动力学、药效学及安全性相关的单核苷酸多态性(SNP)。为此,使用ThermoFisher QuantStudio 12K Flex OpenArray对25名参与生物等效性临床试验的志愿者的21个基因中的67个SNP进行基因分型。统计策略包括单变量分析,该分析先分析这些SNP与药代动力学参数或药物不良反应(ADR)发生情况之间的关联,然后进行Bonferroni校正的多变量回归分析。使用SPSS软件v.21和R commander(版本v3.6.3)进行统计分析。在单变量分析中,分别有14个和16个SNP与美金刚和多奈哌齐的药代动力学参数显著相关。Rs20417()与至少一种ADR的发生有关。然而,在Bonferroni校正的多变量分析中,这些关联均未达到显著性阈值。总之,我们未观察到所分析的SNP与美金刚和多奈哌齐的药代动力学或ADR之间存在任何显著关联。目前关于美金刚和多奈哌齐药物遗传学的证据并不支持将它们纳入药物遗传学指南。