CYP2C19 genotype and sodium channel blockers in lacosamide-treated children with epilepsy: two major determinants of trough lacosamide concentration or clinical response.

IF 5.4 3区 材料科学 Q2 CHEMISTRY, PHYSICAL
ACS Applied Energy Materials Pub Date : 2024-09-19 eCollection Date: 2024-01-01 DOI:10.1177/17562864241273087
Yue Li, Hong-Li Guo, Jie Wang, Yuan-Yuan Zhang, Wei-Jun Wang, Jian Huang, Lin Fan, Ya-Hui Hu, Xiao-Peng Lu, Feng Chen
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引用次数: 0

Abstract

Background: The widespread clinical use of lacosamide (LCM) has revealed significant individual differences in clinical response, with various reported influencing factors. However, it remains unclear how genetic factors related to the disposition and clinical response of LCM, as well as drug-drug interactions (DDIs), exert their influence on pediatric patients with epilepsy.

Objectives: To evaluate the impact of genetic variations and DDIs on plasma LCM concentrations and clinical response.

Design: Patients with epilepsy treated with LCM from June 2021 to March 2023 in the Children's Hospital of Nanjing Medical University were included in the analysis.

Methods: The demographic information and laboratory examination data were obtained from the hospital information system. For the pharmacogenetic study, the left-over blood specimens, collected for routine plasma LCM concentration monitoring, were used to perform genotyping analysis for the selected 26 single nucleotide polymorphisms from 14 genes. The trough concentration/daily dose (C 0/D) ratio and efficacy outcomes were compared.

Results: Patients achieved 90.1% and 68.9% responder rates in LCM mono- and add-on therapy, respectively. The genetic variant in the CYP2C19 *2 (rs4244285) was associated with a better responsive treatment outcome (odds ratio: 1.82; 95% confidence interval: 1.05-3.15; p = 0.031). In monotherapy, 36% of patients were CYP2C19 normal metabolizers (NMs), 49% were intermediate metabolizers (IMs), and 15% were poor metabolizers (PMs) carrying CYP2C19 *2 or *3. Of note, the C 0/D ratios of IMs and PMs were 9.1% and 39.6% higher than those of NMs, respectively. Similar results were in the add-on therapy group, and we also observed a substantial decrease in the C 0/D ratio when patients were concomitant with sodium channel blockers (SCBs).

Conclusion: This study was the first to confirm that CYP2C19 *2 or *3 variants impact the disposition and treatment response of LCM in children with epilepsy. Moreover, concomitant with SCBs, particularly oxcarbazepine, also decreased plasma LCM concentration.

接受拉科酰胺治疗的癫痫患儿的CYP2C19基因型和钠通道阻滞剂:拉科酰胺谷浓度或临床反应的两个主要决定因素。
背景:拉科酰胺(LCM)在临床上的广泛应用表明,临床反应存在显著的个体差异,据报道影响因素多种多样。然而,与LCM的处置和临床反应有关的遗传因素以及药物间相互作用(DDIs)如何对儿科癫痫患者产生影响仍不清楚:评估基因变异和 DDI 对血浆 LCM 浓度和临床反应的影响:分析对象为2021年6月至2023年3月在南京医科大学附属儿童医院接受LCM治疗的癫痫患者:人口统计学信息和实验室检查数据来自医院信息系统。在药物遗传学研究中,使用常规血浆 LCM 浓度监测所采集的剩余血液标本,对所选的 14 个基因中的 26 个单核苷酸多态性进行基因分型分析。对谷浓度/日剂量(C 0/D)比值和疗效进行了比较:结果:在 LCM 单药治疗和附加治疗中,患者的应答率分别为 90.1%和 68.9%。CYP2C19 *2的基因变异(rs4244285)与更好的疗效反应相关(几率比:1.82;95% 置信区间:1.05-3.15;p = 0.031)。在单药治疗中,36% 的患者为 CYP2C19 正常代谢者(NMs),49% 为中等代谢者(IMs),15% 为携带 CYP2C19 *2 或 *3 的不良代谢者(PMs)。值得注意的是,IMs 和 PMs 的 C 0/D 比率分别比 NMs 高 9.1% 和 39.6%。我们还观察到,当患者同时使用钠通道阻滞剂(SCBs)时,C 0/D 比值大幅下降:本研究首次证实,CYP2C19 *2或*3变体会影响癫痫患儿对LCM的处置和治疗反应。此外,同时使用钠通道阻滞剂(尤其是奥卡西平)也会降低血浆中 LCM 的浓度。
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来源期刊
ACS Applied Energy Materials
ACS Applied Energy Materials Materials Science-Materials Chemistry
CiteScore
10.30
自引率
6.20%
发文量
1368
期刊介绍: ACS Applied Energy Materials is an interdisciplinary journal publishing original research covering all aspects of materials, engineering, chemistry, physics and biology relevant to energy conversion and storage. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrate knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important energy applications.
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