Physiologically based pharmacokinetic modeling in obesity: applications and challenges.

Ruwei Yang, Qin Ding, Junjie Ding, Liyong Zhu, Qi Pei
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Abstract

Introduction: Rising global obesity rates pose a threat to people's health. Obesity causes a series of pathophysiologic changes, making the response of patients with obesity to drugs different from that of nonobese, thus affecting the treatment efficacy and even leading to adverse events. Therefore, understanding obesity's effects on pharmacokinetics is essential for the rational use of drugs in patients with obesity.

Areas covered: Articles related to physiologically based pharmacokinetic (PBPK) modeling in patients with obesity from inception to October 2023 were searched in PubMed, Embase, Web of Science and the Cochrane Library. This review outlines PBPK modeling applications in exploring factors influencing obesity's effects on pharmacokinetics, guiding clinical drug development and evaluating and optimizing clinical use of drugs in patients with obesity.

Expert opinion: Obesity-induced pathophysiologic alterations impact drug pharmacokinetics and drug-drug interactions (DDIs), altering drug exposure. However, there is a lack of universal body size indices or quantitative pharmacology models to predict the optimal for the patients with obesity. Therefore, dosage regimens for patients with obesity must consider individual physiological and biochemical information, and clinically individualize therapeutic drug monitoring for highly variable drugs to ensure effective drug dosing and avoid adverse effects.

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基于生理学的肥胖症药物动力学模型:应用与挑战。
导言:全球肥胖率不断上升,对人们的健康构成威胁。肥胖会引起一系列病理生理变化,使肥胖患者对药物的反应与非肥胖患者不同,从而影响治疗效果,甚至导致不良反应。因此,了解肥胖对药代动力学的影响对于肥胖患者合理用药至关重要:本综述在 PubMed、Embase、Web of Science 和 Cochrane Library 中检索了从开始到 2023 年 10 月与肥胖症患者基于生理的药代动力学(PBPK)建模相关的文章。本综述概述了 PBPK 模型在探索肥胖对药代动力学的影响因素、指导临床药物开发以及评估和优化肥胖患者临床用药方面的应用:肥胖引起的病理生理改变会影响药物代谢动力学和药物间相互作用(DDI),从而改变药物暴露。然而,目前还缺乏通用的体型指数或定量药理学模型来预测肥胖症患者的最佳用药。因此,肥胖症患者的用药方案必须考虑个体的生理和生化信息,并在临床上对变化较大的药物进行个体化治疗药物监测,以确保有效用药并避免不良反应。
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