Faculty of Pharmacy and Pharmaceutical Sciences, University of Alberta, Edmonton, AB, Canada.
College of Pharmacy, Seoul National University, Seoul, Republic of Korea.
Br J Clin Pharmacol. 2021 Apr;87(4):1730-1757. doi: 10.1111/bcp.14590. Epub 2021 Feb 2.
Mycophenolic acid (MPA) is widely used in paediatric kidney transplant patients and sometimes prescribed for additional indications. Population pharmacokinetic or pharmacodynamic modelling has been frequently used to characterize the fixed, random and covariate effects of MPA in adult patients. However, MPA population pharmacokinetic data in the paediatric population have not been systematically summarized. The objective of this narrative review was to provide an up-to-date critique of currently available paediatric MPA population pharmacokinetic models, with emphases on modelling techniques, pharmacological findings and clinical relevance. PubMed and EMBASE were searched from inception of database to May 2020, where a total of 11 studies have been identified representing kidney transplant (n = 4), liver transplant (n = 1), haematopoietic stem cell transplant (n = 1), idiopathic nephrotic syndrome (n = 2), systemic lupus erythematosus (n = 2), and a combined population consisted of kidney, liver and haematopoietic stem cell transplant patients (n = 1). Critical analyses were provided in the context of MPA absorption, distribution, metabolism, excretion and bioavailability in this paediatric database. Comparisons to adult patients were also provided. With respect to clinical utility, Bayesian estimation models (n = 6) with acceptable accuracy and precision for MPA exposure determination have also been identified and systematically evaluated. Overall, our analyses have identified unique features of MPA clinical pharmacology in the paediatric population, while recognizing several gaps that still warrant further investigations. This review can be used by pharmacologists and clinicians for improving MPA pharmacokinetic-pharmacodynamic modelling and patient care.
麦考酚酸(MPA)广泛用于儿科肾移植患者,有时也用于其他适应证。群体药代动力学或药效动力学模型已被广泛用于描述成人患者 MPA 的固定、随机和协变量效应。然而,儿科人群中 MPA 的群体药代动力学数据尚未得到系统总结。本叙述性综述的目的是提供对当前可用的儿科 MPA 群体药代动力学模型的最新评价,重点介绍建模技术、药理学发现和临床相关性。从数据库建立到 2020 年 5 月,通过 PubMed 和 EMBASE 进行了搜索,共确定了 11 项研究,分别代表肾移植(n = 4)、肝移植(n = 1)、造血干细胞移植(n = 1)、特发性肾病综合征(n = 2)、系统性红斑狼疮(n = 2),以及由肾、肝和造血干细胞移植患者组成的混合人群(n = 1)。在这个儿科数据库中,对 MPA 的吸收、分布、代谢、排泄和生物利用度进行了批判性分析。还提供了与成人患者的比较。就临床实用性而言,还确定并系统评估了具有可接受的 MPA 暴露测定准确性和精密度的贝叶斯估计模型(n = 6)。总体而言,我们的分析确定了儿科人群中 MPA 临床药理学的独特特征,同时也认识到仍需要进一步研究的几个差距。该综述可被药理学家和临床医生用于改进 MPA 药代动力学-药效动力学模型和患者护理。