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When and How to Use Sodium-Glucose Cotransporter 2 Inhibitors in Patients With Heart Failure With Reduced Ejection
Eileen O'Meara1, Subodh Verma2
1Department of Cardiology, Montréal Heart Institute, Université de Montréal, Montréal, Québec, Canada.
Abstract:
The role of sodium-glucose cotransporter 2 (SGLT2) inhibitors in preventing heart failure (HF) in people with type 2 diabetes (T2DM) is now part of current treatment recommendations. Two large clinical trials (DAPA-HF and EMPEROR-Reduced) have recently highlighted the important impact of SGLT2 inhibitors in patients with HF and a reduced ejection fraction (HFrEF), with significant outcome benefits on HF hospitalisations and cardiovascular mortality, and similar effects in patients with and without T2DM. These benefits were observed on top of excellent background HF therapy, and there were no treatment interactions between SGLT2 inhibitors and background HF therapy. There were no increases in adverse events of interest in the SGLT2 inhibitor arm, including volume depletion, adverse renal events, hypoglycemia, amputation, and ketoacidosis, demonstrating the favourable safety profile of this treatment in HFrEF. Approximately 40%-50% of patients with HFrEF have chronic kidney disease (CKD), and the recently reported results of the DAPA-CKD trial indicate that dapagliflozin can prevent renal and cardiovascular outcomes in patients with established CKD, whether diabetes is present or not. Although the mechanisms of action of SGLT2 inhibitors are not fully understood, the hypotheses that have been proposed for their HF outcome benefits include a reduction of preload via osmotic diuresis, lowering of afterload, reduction in myocardial mass, alteration of myocardial energy substrate toward a more efficient glucose metabolism, modulation of renal sympathetic afferent tone, and increased erythropoiesis. We here present a summary of the evidence as well as a practical perspective on prescribing SGLT2 inhibitors in patients with HFrEF, with or without diabetes.
Insights
Sodium-glucose cotransporter 2 (SGLT2) inhibitors significantly reduce heart failure hospitalizations and cardiovascular mortality in patients with heart failure with reduced ejection fraction (HFrEF). These drugs offer a favorable safety profile, even in patients with chronic kidney disease.
Area of Science:
- Cardiology
- Endocrinology
- Nephrology
Background:
- Sodium-glucose cotransporter 2 (SGLT2) inhibitors are recommended for type 2 diabetes (T2DM) and have shown benefits in heart failure (HF).
- Recent trials like DAPA-HF and EMPEROR-Reduced confirm SGLT2 inhibitors' efficacy in heart failure with reduced ejection fraction (HFrEF).
- These benefits extend to patients with or without T2DM and do not interact with existing HF therapies.
Purpose of the Study:
- To summarize evidence on SGLT2 inhibitors for HFrEF.
- To provide a practical guide for prescribing SGLT2 inhibitors in HFrEF patients.
- To discuss the safety and efficacy of SGLT2 inhibitors in HFrEF, including those with chronic kidney disease (CKD).
Main Methods:
- Review of major clinical trials (DAPA-HF, EMPEROR-Reduced, DAPA-CKD).
- Analysis of outcome benefits on HF hospitalizations and cardiovascular mortality.
- Assessment of safety profile and adverse events.
Main Results:
- SGLT2 inhibitors significantly reduce HF hospitalizations and cardiovascular mortality in HFrEF.
- Benefits are consistent across patients with and without T2DM.
- Favorable safety profile observed, with no increased adverse events of concern.
- Dapagliflozin shows renal and cardiovascular benefits in CKD patients, irrespective of diabetes status.
Conclusions:
- SGLT2 inhibitors are crucial for managing HFrEF, offering significant outcome improvements.
- The favorable safety profile supports their use in a broad HFrEF population, including those with CKD.
- Understanding proposed mechanisms of action may further optimize SGLT2 inhibitor therapy in cardiovascular and renal disease.
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