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Treatment of HFpEF beyond the SGLT2-Is: Does the Addition of GLP-1 RA Improve Cardiometabolic Risk and Outcomes in Diabetic Patients?

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MDPI
DOI: 10.3390/ijms232314598

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heart failure with preserved ejection fraction; phenotypes; SGLT2 inhibitors; GLP1 receptor agonists

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Heart failure with preserved ejection fraction (HFpEF) is a common clinical syndrome, and its incidence is increasing due to an ageing population and the increasing incidence of various diseases. The complexity of HFpEF has made it difficult to identify specific therapies, although some antidiabetic drugs have shown positive effects. There is limited evidence regarding the potential benefits of combined therapy with SGLT2-Is and GLP-1 RAs in HFpEF patients.
Heart failure with preserved ejection fraction (HFpEF) is a common clinical syndrome frequently seen in elderly patients, the incidence of which is steadily increasing due to an ageing population and the increasing incidence of diseases, such as diabetes, hypertension, obesity, chronic renal failure, and so on. It is a multifactorial disease with different phenotypic aspects that share left ventricular diastolic dysfunction, and is the cause of about 50% of hospitalizations for heart failure in the Western world. Due to the complexity of the disease, no specific therapies have been identified for a long time. Sodium-Glucose Co-Transporter 2 Inhibitors (SGLT2-Is) and Glucagon-Like Peptide Receptor Agonists (GLP-1 RAs) are antidiabetic drugs that have been shown to positively affect heart and kidney diseases. For SGLT2-Is, there are precise data on their potential benefits in heart failure with reduced ejection fraction (HFrEF) as well as in HFpEF; however, insufficient evidence is available for GLP-1 RAs. This review addresses the current knowledge on the cardiac effects and potential benefits of combined therapy with SGLT2-Is and GLP-1RAs in patients with HFpEF.

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