{"title":"Clinical Evidence of Kidney Protection Exerted by SGLT2 Inhibitors.","authors":"Anna Solini, Domenico Tricò","doi":"10.1007/164_2026_847","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":12859,"journal":{"name":"Handbook of experimental pharmacology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2026-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Handbook of experimental pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/164_2026_847","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
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.
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.