Preprint Review Version 1 Preserved in Portico This version is not peer-reviewed

Sodium Glucose Co-transporter 2 in Heart Failure: Current Evidence in Special Populations

Version 1 : Received: 21 April 2023 / Approved: 23 April 2023 / Online: 23 April 2023 (03:13:59 CEST)

A peer-reviewed article of this Preprint also exists.

Moady, G.; Ben Gal, T.; Atar, S. Sodium-Glucose Co-Transporter 2 Inhibitors in Heart Failure—Current Evidence in Special Populations. Life 2023, 13, 1256. Moady, G.; Ben Gal, T.; Atar, S. Sodium-Glucose Co-Transporter 2 Inhibitors in Heart Failure—Current Evidence in Special Populations. Life 2023, 13, 1256.

Abstract

Sodium-glucose co-transporter 2 (SGLT2) inhibitors, originally used for diabetes mellitus, are gaining more popularity for other indications owing to their positive cardiovascular and renal effects. Initially, SGLT2 inhibitors were shown to reduce heart failure (HF) hospitalization and improve cardiovascular outcomes in patients with type 2 diabetes. Later, SGLT2 inhibitors were evaluated in patients with HF with reduced ejection fraction (HFREF) and had beneficial effects independent of the presence of diabetes. Recently, reduction in cardiovascular outcomes were also observed in patients with HF with preserved ejection fraction (HFPEF). SGLT2 inhibitors also reduced renal outcomes in patients with chronic kidney disease. Overall, these drugs have an excellent safety profile with a negligible risk of genitourinary tract infections and ketoacidosis. In this review, we discuss the current data regarding SGLT2 inhibitors in special populations including acute myocardial infarction, acute HF, right ventricular (RV) failure, patients with left ventricular assist device (LVAD), and patients with type1 diabetes. We also discuss the potential mechanisms behind the cardiovascular benefits of these drugs.

Keywords

Heart failure; Sodium-glucose co-transporter; diabetes; cardiovascular outcomes.

Subject

Medicine and Pharmacology, Cardiac and Cardiovascular Systems

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