Department of Pharmacy, The Third XiangyHospital, Central South University, Changsha, Hunan, China.
Center for Tropical Medicine and Global Health, Oxford Medical School, Oxford, UK.
Expert Opin Drug Metab Toxicol. 2024 Aug;20(8):805-816. doi: 10.1080/17425255.2024.2388690. Epub 2024 Aug 12.
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.
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.
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.
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不同于非肥胖患者,从而影响治疗效果,甚至导致不良事件。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。
从最初到 2023 年 10 月,在 PubMed、Embase、Web of Science 和 Cochrane Library 中搜索了与肥胖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 建模在探索影响肥胖对药代动力学影响的因素、指导临床药物开发以及评估和优化肥胖患者药物临床应用中的应用。
肥胖引起的病理生理改变会影响药物的药代动力学和药物-药物相互作用(DDI),从而改变药物暴露量。然而,目前缺乏通用的体型指数或定量药理学模型来预测肥胖患者的最佳用药剂量。因此,肥胖患者的剂量方案必须考虑个体的生理和生化信息,并对高度变异性药物进行临床个体化治疗药物监测,以确保有效给药剂量并避免不良反应。