Sodium-glucose cotransporter 2 inhibitors and heart failure: the best timing for the right patient
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Updated: Oct 16, 2025

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Published on: June 11, 2012
Paolo Severino1, Andrea D'Amato2, Silvia Prosperi2
1Department of Clinical, Internal, Anesthesiology and Cardiovascular Sciences, Sapienza University of Rome, Viale del Policlinico, 155, 00161, Rome, Italy. paolo.severino@uniroma1.it.
Insights
Sodium-glucose cotransporter 2 inhibitors (SGLT2i) offer significant cardiovascular benefits, particularly for heart failure (HF) patients. These drugs reduce hospitalizations and mortality, improving quality of life, regardless of diabetes status.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Heart failure (HF) is a complex systemic disease with high mortality.
- Sodium-glucose cotransporter 2 inhibitors (SGLT2i) were initially developed as anti-diabetic drugs.
- SGLT2i demonstrate pleiotropic effects beneficial for cardiovascular health.
Purpose of the Study:
- To review the beneficial effects of SGLT2 inhibitors in heart failure management.
- To highlight the efficacy of SGLT2 inhibitors across various HF stages and patient populations.
Main Methods:
- Review of recent clinical evidence and studies on SGLT2 inhibitors in HF.
- Analysis of data concerning HF hospitalization, mortality, symptoms, and quality of life.
Main Results:
- SGLT2i reduce HF hospitalization and mortality risk in patients with or without diabetes.
- Beneficial effects observed in both chronic HF and acute decompensation.
- Improvements in HF symptoms and quality of life are reported.
Conclusions:
- SGLT2 inhibitors are a valuable therapeutic tool for heart failure.
- Further research is needed to optimize the timing of SGLT2i administration for maximum benefit.
Abstract:
Sodium-glucose cotransporter 2 inhibitors (SGLT2i), initially born as anti-diabetic drugs, have shown many beneficial effects on the cardiovascular system, in particular against heart failure (HF). HF is a complex and multifaceted disease that requires a comprehensive approach. It should not be considered as a simplistic cardiac disease, but a systemic disease that leads to multisystemic organ failure and death. Exploiting their pleiotropic effects, SGLT2i are a very valid tool for HF treatment. Beyond the indication to reduce HF hospitalization and death risk, in patients with diabetes mellitus at high cardiovascular risk or with established cardiovascular event, SGLT2i administration reported beneficial effects regarding the wide spectrum of HF manifestations and stages, independently by diabetes mellitus presence. Recent evidence focuses on HF rehospitalization, cardiac and all-cause death reduction, as well as symptoms and quality of life improvement, in patients with chronic HF or with a recent HF decompensation episode. Given the recent finding about the SGLT2i usefulness in HF patients, further studies are needed to define the best administration timing to maximize the SGLT2i-derived beneficial effects.
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