Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Unidad de Investigación UNAM-INC, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Expert Opin Investig Drugs. 2021 Nov;30(11):1141-1157. doi: 10.1080/13543784.2021.2002844. Epub 2021 Dec 6.
Mineralocorticoid receptor (MR) antagonists (MRAs) provide cardiorenal protection. However steroidal MRAs might induce hyperkalemia and sex hormone-related adverse effects. Several novel non-steroidal MRAs are being developed that are highly selective for the MR and may have an improved safety profile.
This narrative review summarizes data from head-to-head comparisons of emerging non-steroidal MRAs with older steroidal MRAs, including pharmacological characteristics, pharmacokinetic properties, clinical outcomes, and safety, and highlights similarities and differences between emerging agents and established steroidal MRAs.
Head-to-head comparisons in phase 2 trials suggest that the new non-steroidal MRAs exhibit at least equivalent efficacy to steroidal MRAs but may have a better safety profile in patients with heart failure and/or kidney disease. When also taking into account data from recent phase 3 placebo-controlled trials, these novel non-steroidal MRAs have the potential to provide a cardiorenal benefit above that of current optimized standard-of-care treatment in a high-risk population with reduced renal function, and with a lower risk of hyperkalemia. To optimize therapy, further research is needed to clarify the molecular differences in the mode of action of non-steroidal MRAs versus steroidal MRAs, and biomarkers that are predictive of MRA response need to be identified and validated.
盐皮质激素受体 (MR) 拮抗剂 (MRA) 可提供心脏肾脏保护。然而,甾体 MRA 可能引起高钾血症和与性激素相关的不良反应。目前正在开发几种新型非甾体 MRA,它们对 MR 具有高度选择性,可能具有改善的安全性特征。
本综述性文章总结了新型非甾体 MRA 与较老的甾体 MRA 进行头对头比较的研究数据,包括药理学特征、药代动力学特性、临床结局和安全性,并强调了新型药物与已确立的甾体 MRA 之间的相似性和差异性。
2 期试验的头对头比较表明,新型非甾体 MRA 至少与甾体 MRA 具有等效疗效,但在心力衰竭和/或肾病患者中可能具有更好的安全性特征。当同时考虑到最近的 3 期安慰剂对照试验数据时,这些新型非甾体 MRA 有可能在心肾高危人群中,在降低肾功能的情况下,提供优于当前最佳标准治疗的心脏肾脏获益,并且低钾血症风险较低。为了优化治疗,需要进一步研究以阐明非甾体 MRA 与甾体 MRA 的作用模式的分子差异,并需要确定和验证可预测 MRA 反应的生物标志物。