首页> 外文期刊>Current hypertension reports. >Converging indications of aldosterone antagonists (Spironolactone and Eplerenone): A narrative review of safety profiles topical collection on antihypertensive agents: Mechanisms of drug action
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Converging indications of aldosterone antagonists (Spironolactone and Eplerenone): A narrative review of safety profiles topical collection on antihypertensive agents: Mechanisms of drug action

机译:醛固酮拮抗剂(螺内酯和依普利农)的适应症:对降压药局部用药的安全性叙事回顾:药物作用机制

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摘要

The converging clinical effectiveness of mineralocorticoid receptor antagonists (MRAs) Spironolactone and Eplerenone has made their safety profiles/cost-effectiveness key determinants of "agents of choice" across a broad range of clinical indications. The clinical biology of the aldosterone molecule and its range of effects in varied organ systems have been well elucidated from recent mechanistic and systematic studies. Clinical experience with Spironolactone is well established, as is its adverse effects profile. The range of adverse effects experienced with Spironolactone subsequently led to its modification and synthesis of Eplerenone. Recent published reports have confirmed lower prevalence rates of sex-related adverse effects attributable to Eplerenone compared to Spironolactone. There is, however, not much to choose between these agents in regards to other adverse effects including hyperkalemia and kidney failure. As was the experience with Spironolactone, as more robust observational data on Eplerenone accrues, it is possible that the real-life experience of its adverse profile may be discordant with that reported by randomized controlled clinical trials (RCTs). In addition, its metabolism by the vulnerable and highly polymorphic cytochrome dependent pathway also makes it susceptible to various drug interactions. The potential implication of the latter (including morbidity and mortality) may take years to evolve.
机译:盐皮质激素受体拮抗剂(MRA)螺内酯和依普利农的临床疗效融合,已使其安全性/成本效益成为决定各种临床适应症“选择药物”的关键决定因素。最近的机制和系统研究已经很好地阐明了醛固酮分子的临床生物学及其在各种器官系统中的作用范围。螺内酯及其不良反应的临床经验已得到充分确立。螺内酯经历的一系列不良反应随后导致其修饰和合成依普利农。最近发表的报告证实,与螺内酯相比,归因于依普利农的性相关不良反应的患病率较低。但是,就其他副作用(包括高钾血症和肾衰竭)而言,在这些药物之间没有太多选择。与螺内酯的经验一样,随着对依普利农的观察数据的增加,其不良反应的真实生活经验可能与随机对照临床试验(RCT)报道的经验不一致。此外,它通过易受攻击的高度多态性细胞色素依赖性途径代谢也使其易受各种药物相互作用的影响。后者的潜在含义(包括发病率和死亡率)可能需要数年才能演变。

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