Key result
SGLT2 inhibitors reduce heart failure hospitalizations and serious cardiac events across all LVEF ranges.
Why the study?
The expanding use of SGLT2 inhibitors beyond type 2 diabetes to cardiovascular disease and heart failure requires comprehensive evaluation of their benefits and mechanisms.
Do sodium-glucose cotransporter 2 inhibitors improve outcomes in patients with cardiovascular disease, heart failure, type 2 diabetes, and chronic kidney disease?
Do sodium-glucose cotransporter 2 inhibitors improve outcomes in patients with cardiovascular disease, heart failure, type 2 diabetes, and chronic kidney disease?
This review highlights the multisystem benefits of SGLT2 inhibitors, supporting their indication for the treatment of all spectrums of heart failure, type 2 diabetes, and chronic kidney disease.
May support SGLT2 inhibitor use across HF phenotypes; leaves open optimal implementation and long-term outcomes.
AIMS: The use of sodium-glucose cotransporter 2 inhibitors (SGLT2i) as a new class of drug in treating type 2 diabetes has expanded beyond its original framework. Positive results have been achieved in reducing symptoms in patients with cardiovascular disease (CVD). The aim of this article is to present an in-depth review of the basic principles of this class of medications and how it has brought benefits to patients affected particularly by heart failure. METHODS: Following a thorough PubMed search, this review includes 62 studies published between 2015 and 2023. Keywords searched included 'sodium-glucose cotransporter 2 inhibitors', 'cardiovascular disease', 'heart failure', 'chronic kidney disease', and 'type 2 diabetes'. The most recent and comprehensive data were used. RESULTS: Positive results have been achieved in reducing symptoms in patients with CVD. SGLT2 inhibitors have also been shown to be useful in other contexts such as nonalcoholic fatty liver disease (NAFLD) by reducing liver fat accumulation, kidney benefits by improving body weight and vascular endothelium, improving eGFR, and reducing progression to end stage kidney disease (ESKD). SGLT2 inhibitors are also effective in reducing the need for heart failure hospitalizations and the risk of serious cardiac adverse events, including cardiovascular and all-cause mortality, in patients with reduced or preserved left ventricular (LV) ejection fraction and in acute or decompensated settings. CONCLUSION: SGLT2 inhibitors have evolved into metabolic drugs because of their multisystem action and are indicated for the treatment of all spectrums of heart failure, type 2 diabetes, and chronic kidney disease.
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Khater et al. (2024) conducted a review in Cardiovascular disease. Sodium-glucose cotransporter 2 inhibitors (SGLT2i) was evaluated. SGLT2 inhibitors reduce the need for heart failure hospitalizations and the risk of serious cardiac adverse events in patients with reduced or preserved left ventricular ejection fraction.
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