Physiologically based pharmacokinetic models for predicting lamotrigine exposure and dose optimization in pediatric patients receiving combination therapy with carbamazepine or valproic acid.

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Pharmacotherapy Pub Date : 2024-08-29 DOI:10.1002/phar.4603
Zhiwei Liu, Wenxin Shao, Xingwen Wang, Kuo Geng, Wenhui Wang, Yiming Li, Youjun Chen, Haitang Xie
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引用次数: 0

Abstract

Introduction: Lamotrigine (LTG) is an antiepileptic drug that has been used in pediatric epilepsy as a combination therapy or monotherapy after stabilization in recent years. However, there are significant drug-drug interactions (DDI) between LTG and combined drugs such as carbamazepine (CBZ) and valproic acid (VPA). It is particularly important to consider the risk of DDI in combination therapy for intractable epilepsy in pediatric patients. Therefore, it is necessary to adjust the dosage of LTG accordingly. The aim of this study was to establish and validate a pediatric physiologically based pharmacokinetic (PBPK) model for predicting LTG exposure. The model is designed to explore the potential for quantifying pharmacokinetic (PK) DDI of LTG when administered concurrently with CBZ or VPA in pediatric patients.

Method: Adult and pediatric PBPK models for LTG and VPA were developed using PK-Sim® software in combination with physiological information and drug-specific parameters, and a DDI model was developed in combination with the published CBZ model. The models were validated against available PK data.

Results: Predictive and observational results in adults, children, and the DDI model were in good agreement. The recommended doses of LTG for preschool children (2-6 years) and school-aged children (6-12 years) in the absence of drug interactions were 1.47 and 1.2 times higher than those for adults, respectively; 3.1 and 2.6 times higher than those for adults in combination with CBZ; and 0.67 and 0.57 times lower than those for adults in combination with VPA. In addition, plasma exposures in adolescents (12-18 years) were similar to those in adults at the same doses.

Conclusion: We have successfully developed PBPK models and DDI models for LTG in adults and children, which provide a reference for rational drug use in the pediatric population.

基于生理学的药代动力学模型,用于预测接受卡马西平或丙戊酸联合治疗的儿科患者的拉莫三嗪暴露量和剂量优化。
简介拉莫三嗪(LTG)是一种抗癫痫药物,近年来被用于小儿癫痫的联合治疗或病情稳定后的单药治疗。然而,LTG 与卡马西平(CBZ)和丙戊酸(VPA)等联合用药之间存在严重的药物相互作用(DDI)。在对儿童患者的顽固性癫痫进行联合治疗时,考虑 DDI 风险尤为重要。因此,有必要相应地调整 LTG 的剂量。本研究旨在建立并验证一个儿科生理药代动力学(PBPK)模型,用于预测LTG的暴露量。该模型旨在探索在儿科患者中,当LTG与CBZ或VPA同时给药时,量化药代动力学(PK)DDI的可能性:方法:结合生理信息和药物特异性参数,使用 PK-Sim® 软件开发了 LTG 和 VPA 的成人和儿科 PBPK 模型,并结合已发表的 CBZ 模型开发了 DDI 模型。根据现有的 PK 数据对这些模型进行了验证:结果:成人、儿童的预测结果和观察结果与 DDI 模型非常吻合。在没有药物相互作用的情况下,学龄前儿童(2-6 岁)和学龄儿童(6-12 岁)的 LTG 推荐剂量分别是成人的 1.47 倍和 1.2 倍;是成人与 CBZ 联用时的 3.1 倍和 2.6 倍;是成人与 VPA 联用时的 0.67 倍和 0.57 倍。此外,在相同剂量下,青少年(12-18 岁)的血浆暴露量与成人相似:我们成功建立了LTG在成人和儿童中的PBPK模型和DDI模型,为儿科人群的合理用药提供了参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmacotherapy
Pharmacotherapy 医学-药学
CiteScore
7.80
自引率
2.40%
发文量
93
审稿时长
4-8 weeks
期刊介绍: Pharmacotherapy is devoted to publication of original research articles on all aspects of human pharmacology and review articles on drugs and drug therapy. The Editors and Editorial Board invite original research reports on pharmacokinetic, bioavailability, and drug interaction studies, clinical trials, investigations of specific pharmacological properties of drugs, and related topics.
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