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Updated: Jun 14, 2025

Evaluation of Cardiac Contractility Modulation Therapy in 2D Human Stem Cell-Derived Cardiomyocytes
Published on: December 16, 2022
[Current Use of Sodium Glucose Co-transporter 2 Inhibitors in Heart Failure Therapy]
Yüksel Çavuşoğlu1, Hakan Altay2, Ahmet Çelik3
1Department of Cardiology, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Türkiye.
Abstract:
Sodium-glucose cotransporter-2 inhibitors (SGLT2i) inhibit urinary glucose and sodium reabsorption in the proximal tubule of the nephron and result in glucosuria, natriuresis and diuresis. In patients with T2DM who have atherosclerotic cardiovascular (CV) disease or CV risk factors, SGLT2is have been shown to reduce major CV events and heart failure (HF) hospitalization. The greatest and most consistent effect of SGLT2is in these trials was found to be reduction in HF hospitalization, which raised the possibility of clinical benefit of SGLT2i in HF patients. In DAPA-HF and EMPEROR-Reduced trials in HFrEF patients with or without T2DM, SGLT2is, dapagliflozin and empagliflozin treatment on top of standard HF therapy has been shown to have clear clinical benefit in reducing primary endpoint of CV mortality or HF hospitalization and improving quality of life. Recently published EMPEROR-Preserved and DELIVER trials showed that SGLT2is were also very effective in the treatment of HFpEF (EF >40%). Furthermore, SGLT2is have also been shown to have potential in improving clinical outcomes in hospitalized acute HF patients in EMPULSE and DICTATE-AHF trials. All of this evidence has changed guidelines recommended therapies, not only for HFrEF but also for HFpEF treatment. The aim of this article is to provide a comprehensive overview focused on the role of SGLT2i in the treatment of HF based on the recent evidence.
Insights
Sodium-glucose cotransporter-2 inhibitors (SGLT2i) offer significant benefits for heart failure (HF) patients, reducing hospitalizations and improving quality of life. These findings have led to updated treatment guidelines for HF, including HF with reduced ejection fraction (HFrEF) and HF with preserved ejection fraction (HFpEF).
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Sodium-glucose cotransporter-2 inhibitors (SGLT2i) are known for their glucose-lowering effects in type 2 diabetes mellitus (T2DM).
- Previous studies indicated SGLT2i reduce cardiovascular events and heart failure (HF) hospitalizations in T2DM patients with cardiovascular disease or risk factors.
- A notable reduction in HF hospitalizations suggested potential benefits for HF patients.
Purpose of the Study:
- To provide a comprehensive overview of the role of SGLT2 inhibitors in treating heart failure.
- To synthesize recent evidence on SGLT2i efficacy across different HF populations.
Main Methods:
- Review of clinical trial data, including DAPA-HF, EMPEROR-Reduced, EMPEROR-Preserved, DELIVER, EMPULSE, and DICTATE-AHF.
- Analysis of SGLT2i effects on cardiovascular mortality, HF hospitalizations, and quality of life in HFrEF, HFpEF, and acute HF patients.
Main Results:
- SGLT2 inhibitors demonstrated clear clinical benefits in HFrEF patients, reducing HF hospitalizations and improving quality of life.
- Recent trials confirmed SGLT2i efficacy in HFpEF patients (EMPEROR-Preserved, DELIVER).
- Evidence also supports SGLT2i use in hospitalized acute HF patients (EMPULSE, DICTATE-AHF).
Conclusions:
- SGLT2 inhibitors are now a cornerstone therapy for heart failure, impacting treatment guidelines for both HFrEF and HFpEF.
- The evidence supports the expanded use of SGLT2 inhibitors beyond diabetes management into HF treatment.
- SGLT2 inhibitors represent a significant advancement in managing diverse forms of heart failure.
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