Why the study?
Following proven cardiovascular and renal benefits of SGLT2 inhibitors in diabetes and heart failure, current evidence warranted discussion in special populations.
This review summarizes the current evidence and potential mechanisms for the cardiovascular benefits of SGLT2 inhibitors in special populations such as acute MI, acute HF, RV failure, LVAD, and type 1 diabetes.
Cautions against routine SGLT2 inhibitor use in acute MI, HF, or type 1 diabetes; leaves open need for dedicated RCTs.
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.
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Moady et al. (2023) studied this question.
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