Key result
SGLT2 inhibitors reduce HFpEF hospitalizations and symptoms while GLP-1 agonists show promise for concurrent obesity.
Why the study?
Heart failure with preserved ejection fraction presents significant diagnostic and therapeutic challenges due to its heterogeneous etiology and pathophysiology.
What is the efficacy and clinical utility of current and emerging pharmacological therapies for HFpEF?
What is the efficacy and clinical utility of current and emerging pharmacological therapies for HFpEF?
SGLT2 inhibitors and GLP-1 agonists are emerging as promising therapies for HFpEF, highlighting the need for personalized treatment approaches.
May inform personalized HFpEF therapy selection; leaves open definitive GLP-1 roles pending randomized trials.
Heart failure with preserved ejection fraction (HFpEF) is a complex clinical syndrome characterized by diastolic dysfunction and high morbidity. It presents significant challenges in diagnosis and treatment due to its heterogeneous etiology and pathophysiology. This review evaluates the efficacy and clinical utility of current and emerging pharmacological therapies for HFpEF, emphasizing personalized approaches to improve patient outcomes. A comprehensive analysis of literature was conducted to assess the role of established treatments, such as diuretics, RAAS inhibitors, and beta-blockers, alongside emerging therapies, including sodium-glucose cotransporter-2 (SGLT2) inhibitors, glucagon-like peptide-1 (GLP-1) agonists, and novel agents like mavacamten. SGLT2 inhibitors have demonstrated significant reductions in heart failure hospitalizations and symptom burden, while GLP-1 agonists show promise in managing HFpEF with obesity or metabolic syndrome. Mineralocorticoid receptor antagonists provide benefits in selecting patients, although broader therapeutic options remain limited. Other novel agents, such as nitrates and PDE-5 inhibitors, require further validation through clinical trials. HFpEF management demands a multifaceted approach combining lifestyle interventions, optimized pharmacotherapy, and emerging therapeutic strategies. Personalized treatment plans and continued research are vital for addressing the complexities of this syndrome and improving patient outcomes.
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Agrawal et al. (2025) conducted a review in Heart failure with preserved ejection fraction (HFpEF). Pharmacological therapies (SGLT2 inhibitors, GLP-1 agonists, mavacamten) was evaluated. SGLT2 inhibitors reduce heart failure hospitalizations and symptom burden in HFpEF, while GLP-1 agonists show promise in managing patients with concurrent obesity or metabolic syndrome.
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