Literature DB >> 30843294

Sodium glucose cotransporter (SGLT)-2 inhibitors: Do we need them for glucose-lowering, for cardiorenal protection or both?

Rosalie A Scholtes1, Michaël J B van Baar1, Yuliya Lytvyn2, Petter Bjornstad3,4, Max Nieuwdorp1,5, David Z I Cherney2, Daniël H van Raalte1,5.   

Abstract

Sodium glucose cotransporter (SGLT)-2 inhibitors are the newest addition to our treatment armamentarium for the management of hyperglycemia in type 2 diabetes. Glucose-lowering per se reduces the risk of microvascular complications, but not the risk of cardiovascular disease, including heart failure and cardiovascular mortality. Also, even when embedded in optimal cardiovascular prevention, a large residual risk remains with respect to progression of diabetic kidney disease. SGLT-2 inhibitors lower blood glucose levels by inducing glucosuria. Through various proposed mechanisms, among which diuretic and natriuretic effects, SGLT-2 inhibitors decrease heart failure hospitalization, reduce cardiovascular mortality, and mitigate progression of diabetic kidney disease. In this perspective, we will discuss the glucose-lowering and other protective effects of SGLT-2 inhibitors on the cardiorenal axis, both in primary and secondary prevention. By comparing the glycemic and pleiotropic effects of these agents to other glucose-lowering drugs, we will address questions around whether SGLT-2 inhibitors should be considered primarily as glucose-lowering agents, cardiorenal drugs or both.
© 2019 John Wiley & Sons Ltd.

Entities:  

Keywords:  SGLT-2 inhibition; diabetic kidney disease; glycemic control; heart failure; number-needed-to-treat; primary prevention; secondary prevention

Mesh:

Substances:

Year:  2019        PMID: 30843294      PMCID: PMC7045873          DOI: 10.1111/dom.13692

Source DB:  PubMed          Journal:  Diabetes Obes Metab        ISSN: 1462-8902            Impact factor:   6.577


  77 in total

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2.  Long-term effects of intensive glucose lowering on cardiovascular outcomes.

Authors:  Hertzel C Gerstein; Michael E Miller; Saul Genuth; Faramarz Ismail-Beigi; John B Buse; David C Goff; Jeffrey L Probstfield; William C Cushman; Henry N Ginsberg; J Thomas Bigger; Richard H Grimm; Robert P Byington; Yves D Rosenberg; William T Friedewald
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Journal:  Lancet Diabetes Endocrinol       Date:  2018-02-28       Impact factor: 32.069

4.  A sodium-glucose cotransporter 2 inhibitor attenuates renal capillary injury and fibrosis by a vascular endothelial growth factor-dependent pathway after renal injury in mice.

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Journal:  Kidney Int       Date:  2018-07-23       Impact factor: 10.612

5.  Albiglutide and cardiovascular outcomes in patients with type 2 diabetes and cardiovascular disease (Harmony Outcomes): a double-blind, randomised placebo-controlled trial.

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Journal:  Lancet       Date:  2018-10-02       Impact factor: 79.321

6.  Effect of intensive control of glucose on cardiovascular outcomes and death in patients with diabetes mellitus: a meta-analysis of randomised controlled trials.

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Review 9.  New Diabetes Therapies and Diabetic Kidney Disease Progression: the Role of SGLT-2 Inhibitors.

Authors:  Claire C J Dekkers; Ron T Gansevoort; Hiddo J L Heerspink
Journal:  Curr Diab Rep       Date:  2018-03-27       Impact factor: 4.810

Review 10.  Cardiovascular Effects of New Oral Glucose-Lowering Agents: DPP-4 and SGLT-2 Inhibitors.

Authors:  André J Scheen
Journal:  Circ Res       Date:  2018-05-11       Impact factor: 17.367

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  4 in total

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Journal:  PeerJ       Date:  2020-11-17       Impact factor: 2.984

3.  Effects of the sodium-glucose co-transporter-2 inhibitor dapagliflozin on estimated plasma volume in patients with type 2 diabetes.

Authors:  Claire C J Dekkers; C David Sjöström; Peter J Greasley; Valerie Cain; David W Boulton; Hiddo J L Heerspink
Journal:  Diabetes Obes Metab       Date:  2019-09-17       Impact factor: 6.577

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