Faculty of Pharmacy and Pharmaceutical Sciences, University of Alberta, Katz Group Centre for Pharmacy and Health Research, Room 3-142D, 11361-87 Avenue, Edmonton, AB, T6G 2E1, Canada.
Clin Pharmacokinet. 2023 Feb;62(2):157-207. doi: 10.1007/s40262-023-01212-y. Epub 2023 Feb 27.
Corticosteroids (steroids) are commonly used concurrently with mycophenolic acid (MPA) as the first-line immunosuppression therapy for the prevention of rejection in solid organ transplantations. Steroids are also commonly administered with MPA in various autoimmune disorders such as systemic lupus erythematosus and idiopathic nephrotic syndrome. Despite various review articles having suggested the presence of pharmacokinetic interactions between MPA and steroids, definitive data have not yet been demonstrated. The aim of this Current Opinion is to critically evaluate the available clinical data and propose the optimal study design for characterising the MPA-steroid pharmacokinetic interactions. The PubMed and Embase databases were searched for relevant clinical articles in English as of September 29, 2022, where a total of 8 papers have been identified as supporting and 22 as non-supporting the purported drug interaction. To objectively evaluate the data, novel assessment criteria to effectively diagnose the interaction based on known MPA pharmacology were formulated, including the availability of independent control groups, prednisolone concentrations, MPA metabolite data, unbound MPA concentrations, and the characterisations of entero-hepatic recirculation and MPA renal clearance. Overall, the majority of the identified corticosteroid data were pertaining to prednisone or prednisolone. Our assessment indicated that no conclusive mechanistic data supporting the interaction are available in the current clinical literature, and further studies are required to quantify the effects/mechanisms of steroid-tapering or withdrawal on MPA pharmacokinetics. This current opinion provides justification for further translational investigations, as this particular drug interaction has the potential to exert significant adverse outcomes in patients prescribed MPA.
皮质类固醇(类固醇)常与霉酚酸(MPA)联合用于预防实体器官移植中的排斥反应,作为一线免疫抑制治疗。类固醇也常与 MPA 联合用于各种自身免疫性疾病,如系统性红斑狼疮和特发性肾病综合征。尽管有各种综述文章表明 MPA 和类固醇之间存在药代动力学相互作用,但尚未证实明确的数据。本综述旨在批判性地评估现有临床数据,并提出最佳研究设计,以确定 MPA-类固醇药代动力学相互作用。截至 2022 年 9 月 29 日,检索了英文相关临床文献,共确定 8 篇文章支持,22 篇文章不支持所谓的药物相互作用。为了客观评估数据,根据已知的 MPA 药理学制定了新的评估标准,以有效诊断基于已知 MPA 药理学的相互作用,包括独立对照组的可用性、泼尼松龙浓度、MPA 代谢物数据、游离 MPA 浓度以及肠肝再循环和 MPA 肾清除率的特征。总体而言,大多数已确定的皮质类固醇数据与泼尼松或泼尼松龙有关。我们的评估表明,目前的临床文献中没有支持相互作用的明确机制数据,需要进一步研究来量化类固醇减量或停药对 MPA 药代动力学的影响/机制。本综述提供了进一步转化研究的理由,因为这种特定的药物相互作用有可能对服用 MPA 的患者产生重大不良后果。