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Improving heart failure outcomes with sodium-glucose cotransporter 2 inhibitors in different patient groups
1BHF Glasgow Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.
Abstract:
Sodium-glucose cotransporter 2 inhibitors (SGLT-2is) were originally developed for the treatment of hyperglycaemia in type 2 diabetes. Because of regulatory requirements to show the safety of this new class of drugs, a large randomized cardiovascular (CV) outcomes trial was completed but this showed that instead of having a neutral effect on heart failure (HF) outcomes, that these drugs could reduce HF outcomes in this population. Subsequent trials with SGLT-2is have shown that HF hospitalizations are reduced by 30% and CV death or HF hospitalization by 21% in patients with type 2 diabetes. These findings have extended to patients with HF with reduced and mildly reduced or preserved ejection fraction in whom further HF hospitalizations are reduced by 28% and CV death or HF hospitalizations reduced by 23%, and that it is becoming a central therapy for the treatment of HF. Moreover, the benefit in patients with HF is observed regardless of the presence or absence of type 2 diabetes. Similarly, in patients with chronic kidney disease and albuminuria, with and without type 2 diabetes, the benefit of SGLT-2is is clearly seen with a 44% reduction in HF hospitalization and 25% reduction in CV death or HF hospitalization. These trials support the use of SGLT-2is in improving HF outcomes in a broad range of patients, from those with type 2 diabetes, chronic kidney disease and those with pre-existing HF regardless of ejection fraction.
Insights
Sodium-glucose cotransporter 2 inhibitors (SGLT-2is) significantly reduce heart failure hospitalizations and cardiovascular events. These benefits apply to patients with type 2 diabetes, heart failure, and chronic kidney disease, regardless of diabetes status.
Area of Science:
- Cardiology
- Nephrology
- Endocrinology
Background:
- Sodium-glucose cotransporter 2 inhibitors (SGLT-2is) were initially developed for type 2 diabetes management.
- Cardiovascular (CV) outcomes trials revealed unexpected benefits for heart failure (HF) beyond glycemic control.
Purpose of the Study:
- To evaluate the efficacy of SGLT-2 inhibitors in reducing HF hospitalizations and CV death.
- To assess the impact of SGLT-2 inhibitors across diverse patient populations, including those with and without type 2 diabetes and chronic kidney disease.
Main Methods:
- Analysis of data from large, randomized CV outcomes trials and subsequent SGLT-2 inhibitor trials.
- Inclusion of patients with type 2 diabetes, HF with varying ejection fractions, and chronic kidney disease with albuminuria.
Main Results:
- SGLT-2is reduced HF hospitalizations by 30% and CV death or HF hospitalization by 21% in type 2 diabetes patients.
- In HF patients (reduced, mildly reduced, or preserved ejection fraction), HF hospitalizations decreased by 28%, and CV death or HF hospitalization by 23%.
- In chronic kidney disease patients with albuminuria, SGLT-2is led to a 44% reduction in HF hospitalization and a 25% reduction in CV death or HF hospitalization.
Conclusions:
- SGLT-2 inhibitors are effective in improving HF outcomes in a broad patient spectrum.
- The benefits of SGLT-2 inhibitors in HF are observed irrespective of the presence or absence of type 2 diabetes.
- SGLT-2 inhibitors are emerging as a central therapy for HF treatment and are supported for use in patients with type 2 diabetes, CKD, and HF.
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