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Cardio-Protective Effects of Sodium-Glucose Co-Transporter 2 Inhibitors: Focus on Heart Failure
Dimos Karangelis1, C David Mazer2, Dimitrios Stakos3
1Department of Cardiac Surgery, Mitera Hospital, 6 Erythrou Stavrou Street, 15123, Marousi, Athens, Greece.
Background:
Type 2 diabetes mellitus (DM) is associated with a considerable risk of cardiovascular and renal diseases, including heart failure. Sodium-glucose co-transporter 2 (SGLT2) inhibitors have demonstrated unprecedented cardiorenal protective effects in large-scale clinical trials of patients with or without diabetes and either established cardiovascular disease (CV) or multiple CV risk factors.
Objective:
Herein we aim to focus on the role of SGLT2 inhibitors regarding the improvement in heart failure outcomes and the proposed mechanisms of action by which these drugs confer their beneficial effect.
Methods:
PubMed, Embase, and Google Scholar databases were searched to identify eligible articles that are comprehensively summarized and discussed in this study.
Results:
The most commonly discussed mechanisms of action are diuresis and natriuresis, reduction in preload, afterload, and ventricular mass, as well as stimulation of erythropoietin production and improved myocardial energetics. SGLT2 inhibitors improve outcomes in patients with established heart failure (HF) and reduce the risk of death and HF admissions in patients with established chronic HF with reduced ejection fraction (HFrEF), either with or without diabetes.
Conclusion:
Potential key mechanisms that may explain the notable cardioprotective benefits of SGLT2 inhibitors have been outlined. These agents have recently received class Ia recommendation in specific groups of people with DM to lower the risk of hospitalization for HF and risk of death, while these benefits may also extend to people without diabetes. It remains to be seen whether they will also emerge as treatment approaches in the acute phase of CV episodes.
Insights
Sodium-glucose co-transporter 2 (SGLT2) inhibitors show significant heart failure benefits for patients with or without type 2 diabetes. These drugs reduce cardiovascular events and hospitalizations through various mechanisms, including diuresis and improved cardiac energetics.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- Type 2 diabetes mellitus (DM) significantly increases cardiovascular and renal disease risk, particularly heart failure.
- Sodium-glucose co-transporter 2 (SGLT2) inhibitors demonstrate remarkable cardiorenal protective effects in diverse patient populations.
- These benefits are observed in patients with or without diabetes, established cardiovascular disease, or multiple cardiovascular risk factors.
Purpose of the Study:
- To review the role of SGLT2 inhibitors in improving heart failure outcomes.
- To elucidate the proposed mechanisms of action behind the beneficial effects of SGLT2 inhibitors.
Main Methods:
- Comprehensive literature search of PubMed, Embase, and Google Scholar databases.
- Identification and summarization of eligible articles discussing SGLT2 inhibitors and heart failure.
- Focus on mechanisms and clinical outcomes.
Main Results:
- Key mechanisms include diuresis, natriuresis, reduced preload/afterload, decreased ventricular mass, erythropoietin stimulation, and enhanced myocardial energetics.
- SGLT2 inhibitors improve outcomes in patients with established heart failure (HF).
- These agents reduce mortality and HF hospitalizations in chronic heart failure with reduced ejection fraction (HFrEF), irrespective of diabetes status.
Conclusions:
- SGLT2 inhibitors offer significant cardioprotective benefits, with potential mechanisms outlined.
- Class Ia recommendations support SGLT2 inhibitors for reducing HF hospitalizations and mortality in specific type 2 diabetes groups.
- The benefits of SGLT2 inhibitors may extend to non-diabetic individuals, with ongoing research into their use in acute cardiovascular episodes.
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