Mogi Masaki
Department of Pharmacology, Ehime University, Graduate School of Medicine, Shitsukawa, Tohon, Ehime, 791-0295, Japan.
Hypertens Res. 2022 Jun;45(6):967-975. doi: 10.1038/s41440-022-00913-4. Epub 2022 Apr 14.
Aldosterone (Aldo) breakthrough is a well-known phenomenon that occurs in patients with long-term renin-angiotensin aldosterone system (RAAS) blockade using inhibitors of renin or angiotensin converting enzyme or angiotensin II type 1 receptor blockers. The blockade of the mineralocorticoid receptor (MR), an Aldo binding receptor, is effective in managing patients with resistant hypertension, defined as uncontrollable blood pressure despite the concurrent use of three antihypertensive drugs. In other words, MR inhibitors are not used as first-line antihypertensive drugs in most guidelines for hypertension management. Aldo breakthrough puts hypertensive patients at higher risk of cardiovascular disease and worsens future outcomes. This review discusses Aldo secretion and the mechanism of Aldo breakthrough, dependent or independent of the RAAS, with consideration of the pharmacological aspects of this phenomenon, as well as hypothetical views.
醛固酮(Aldo)突破是一种众所周知的现象,发生在长期使用肾素抑制剂、血管紧张素转换酶抑制剂或血管紧张素II 1型受体阻滞剂阻断肾素-血管紧张素-醛固酮系统(RAAS)的患者中。盐皮质激素受体(MR)是一种醛固酮结合受体,阻断该受体对治疗顽固性高血压患者有效,顽固性高血压定义为尽管同时使用三种抗高血压药物但血压仍无法控制。换句话说,在大多数高血压管理指南中,MR抑制剂不作为一线抗高血压药物使用。醛固酮突破使高血压患者面临更高的心血管疾病风险,并使未来预后恶化。本综述讨论了醛固酮分泌以及醛固酮突破的机制,该机制是否依赖于RAAS,同时考虑了这一现象的药理学方面以及一些假设观点。