Khan Safeer, Kalam Muhammad Nasir, Khalid Maryam, Mehmood Malik Hassan, Malik Usman Rashid, Ali Syed Muhammad
Faculty of Pharmacy, The University of Lahore, Lahore, Punjab, Pakistan.
Department of Pharmaceutical Sciences, Government College University, Lahore, Pakistan.
Eur J Drug Metab Pharmacokinet. 2025 Sep 27. doi: 10.1007/s13318-025-00967-y.
Cachexia is a complex multi-organ syndrome characterized by systemic alterations that could impact drug pharmacokinetics. This scoping review aims to examine and synthesize existing research on the pathophysiological changes in cachexia that may influence drug pharmacokinetics.
A comprehensive literature search was conducted across five databases from inception to December 2024. Study selection was refined using the population, concept, and context (PCC) framework. The population included humans and animals with cachexia, the concept focused on cachexia-induced pathophysiological changes in relation to drug pharmacokinetics, and the context encompassed any clinical, healthcare setting, or laboratory settings.
Out of 2684 identified studies, 53 met the inclusion criteria: 25 were based on human data, 18 on animal data, and 10 were reviews. The findings suggest that cachexia may impair drug absorption due to reduced skinfold thickness, gut dysbiosis, and structural and functional alterations in the gastrointestinal (GI) tract. Similarly, drug distribution may also be affected by changes in body composition and decreased serum albumin levels.
Pathophysiological changes in cachexia may lead to alterations in drug absorption and distribution, contributing to variability in drug bioavailability. However, the lack of controlled clinical trials directly linking cachexia-induced physiological changes to specific drug pharmacokinetics renders these findings tentative.
恶病质是一种复杂的多器官综合征,其特征是可能影响药物药代动力学的全身改变。本综述旨在审视和综合现有的关于恶病质病理生理变化可能影响药物药代动力学的研究。
从数据库创建到2024年12月,在五个数据库中进行了全面的文献检索。使用人群、概念和背景(PCC)框架对研究选择进行了细化。人群包括患有恶病质的人类和动物,概念聚焦于恶病质引起的与药物药代动力学相关的病理生理变化,背景涵盖任何临床、医疗环境或实验室环境。
在2684项已识别的研究中,53项符合纳入标准:25项基于人类数据,18项基于动物数据,10项为综述。研究结果表明,恶病质可能由于皮褶厚度减少、肠道菌群失调以及胃肠道(GI)结构和功能改变而损害药物吸收。同样,药物分布也可能受到身体成分变化和血清白蛋白水平降低的影响。
恶病质的病理生理变化可能导致药物吸收和分布的改变,从而导致药物生物利用度的变异性。然而,缺乏将恶病质引起的生理变化与特定药物药代动力学直接联系起来的对照临床试验,使得这些发现具有不确定性。