[不含糖尿病的«糖尿病药物»:SGLT-2抑制剂]。

Q4 Medicine
Praxis Pub Date : 2023-08-01
Danaë Parianos, Matthias Hermann
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引用次数: 0

摘要

引言:在过去的十年里,没有其他类别的药物能像钠-葡萄糖连接转运蛋白2抑制剂(SGLT-2i)或格列吡嗪那样引起如此大的轰动。最近,由于最初作为糖尿病药物开发的SGLT-2i在关键研究中出人意料地也显示出对心脏和肾脏的保护作用,它们现在成了人们谈论的话题。尽管细胞和分子机制尚未完全阐明,但它们已经彻底改变了糖尿病、不依赖于左心室射血分数的心力衰竭和基于现有积极数据的肾病的治疗方法。本文的目的是综述SGLT-2抑制剂的作用和假定的作用机制,特别是在心力衰竭和肾衰竭中,并概述其潜在的风险和副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[«Diabetes Drugs» without Diabetes: SGLT-2 Inhibitors].

Introduction: No other class of drugs has caused as much of a stir in the last decade as sodium-glucose linked transporter 2 inhibitors (SGLT-2i) or gliflozines. At the latest since the SGLT-2i originally developed as a diabetes mellitus drug unexpectedly also showed protective effects for heart and kidney in pivotal studies, they are now the talk of the town. Although the cellular and molecular mechanisms have not yet been clarified in all details, they have revolutionized therapeutic approaches for diabetes mellitus, heart failure independent of left ventricular ejection fraction, and nephropathies based on positive data available. The purpose of this article is to review the effects and postulated mechanisms of action of SGLT-2 inhibitors, particularly in heart failure and renal failure, and to outline their potential risks and side effects.

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来源期刊
Praxis
Praxis Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
146
审稿时长
12 weeks
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