Clinical Evidence of Kidney Protection Exerted by SGLT2 Inhibitors.

Q1 Pharmacology, Toxicology and Pharmaceutics
Anna Solini, Domenico Tricò
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引用次数: 0

Abstract

Sodium-glucose cotransporter-2 inhibitors (SGLT2i) have become foundational therapies for nephroprotection, transforming the management of chronic kidney disease (CKD) beyond the traditional risk factors. This chapter synthesizes evidence from randomized controlled trials and real-world studies demonstrating that SGLT2i consistently reduce albuminuria, slow estimated glomerular filtration rate (eGFR) decline, and lower the risk of hard renal endpoints, including progression to end-stage kidney disease. Early cardiovascular outcome trials first signalled renal benefit as secondary outcomes, which was subsequently confirmed in dedicated renal trials such as CREDENCE, DAPA-CKD, and EMPA-KIDNEY, establishing kidney protection in patients with and without type 2 diabetes and across a broad spectrum of eGFR and albuminuria. Heart failure trials further support renal preservation in high cardiorenal-risk populations. Complementary real-world evidence across multiple health systems corroborates trial findings, extending effectiveness to heterogeneous populations, including older adults and nondiabetic CKD. The chapter also reviews emerging data on combination strategies with GLP-1 receptor agonists or finerenone, long-term treatment considerations, and projections suggesting substantial delays in kidney failure with earlier initiation. Collectively, these data support broad implementation of SGLT2i as core disease-modifying therapy in CKD, while highlighting priority areas for future research in underrepresented populations and optimized combination regimens.

SGLT2抑制剂对肾脏保护作用的临床证据
钠-葡萄糖共转运蛋白-2抑制剂(SGLT2i)已经成为肾脏保护的基础疗法,改变了慢性肾脏疾病(CKD)的管理,超越了传统的危险因素。本章综合了来自随机对照试验和现实世界研究的证据,证明SGLT2i持续降低蛋白尿,减缓肾小球滤过率(eGFR)的估计下降,降低硬肾终点的风险,包括进展为终末期肾脏疾病。早期心血管结局试验首先将肾脏益处作为次要结局,随后在专门的肾脏试验(如CREDENCE、DAPA-CKD和EMPA-KIDNEY)中得到证实,在有2型糖尿病和无2型糖尿病患者以及广泛的eGFR和蛋白尿患者中建立肾脏保护。心力衰竭试验进一步支持在高危人群中保留肾脏。来自多个卫生系统的补充性真实证据证实了试验结果,将有效性扩展到异质人群,包括老年人和非糖尿病性CKD。本章还回顾了GLP-1受体激动剂或芬尼酮联合策略的新数据,长期治疗的考虑,以及提示早期肾衰竭的实质性延迟的预测。总的来说,这些数据支持SGLT2i作为CKD核心疾病改善疗法的广泛实施,同时强调了未来研究的优先领域,即在代表性不足的人群和优化的联合方案中。
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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来源期刊
Handbook of experimental pharmacology
Handbook of experimental pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
5.20
自引率
0.00%
发文量
54
期刊介绍: The Handbook of Experimental Pharmacology is one of the most authoritative and influential book series in pharmacology. It provides critical and comprehensive discussions of the most significant areas of pharmacological research, written by leading international authorities. Each volume in the series represents the most informative and contemporary account of its subject available, making it an unrivalled reference source.
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