Controversy over renin–angiotensin–aldosterone system (RAAS) inhibitors treatment in nephrology and cardiovascular diseases

Pub Date : 2020-01-01 DOI:10.5603/AH.A2020.0007
Rafał Donderski, R. Bednarski, J. Manitius
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引用次数: 3

Abstract

Drugs that act by inhibiting the renin–angiotensin–aldosterone system (RAAS), such as angiotensin-converting enzyme inhibitors (ACE-Is) and angiotensin II receptor type 1 (AT1) blockers (ARBs), have been recognized as a basic canon of nephroprotection for years. They are commonly used in monotherapy for glomerulonephritis with proteinuria. At present, they are rarely used in combination therapy in a form of dual blockade of RAAS due to concern about possible side effects. On the other hand, both ACE-Is and ARBs are also wrongly referred to as nephrotoxic drugs. The significance of therapy with these drugs is seen in evoking acute kidney injury (AKI) or acceleration of CKD. The aim of this article was to clarify the opinion on the relationship between ACE-Is or ARBs treatment and AKI occurrence, and to attempt to reassess the role of dual RAAS blockade in the treatment of kidney diseases. The principles of heart failure (HF) therapy with ACE-Is or ARBs and current data on the importance of RAAS dual blockade in hypertension are also discussed.
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肾素-血管紧张素-醛固酮系统(RAAS)抑制剂治疗肾病和心血管疾病的争议
通过抑制肾素-血管紧张素-醛固酮系统(RAAS)起作用的药物,如血管紧张素转换酶抑制剂(ACE-Is)和血管紧张素II受体1型(AT1)阻滞剂(ARBs),多年来一直被认为是肾保护的基本标准。它们通常用于合并蛋白尿的肾小球肾炎的单药治疗。目前,由于担心可能的副作用,它们很少以双重阻断RAAS的形式用于联合治疗。另一方面,ACE-Is和arb也被错误地称为肾毒性药物。这些药物治疗的意义在于引起急性肾损伤(AKI)或加速CKD。本文旨在阐明ACE-Is或ARBs治疗与AKI发生之间的关系,并试图重新评估双重RAAS阻断在肾脏疾病治疗中的作用。本文还讨论了ACE-Is或arb治疗心力衰竭(HF)的原理,以及目前关于RAAS双重阻断在高血压中的重要性的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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