Key result
HFpEF carries a ~35% two-year hospitalization rate and significant mortality.
Why the study?
Cardiometabolic HFpEF lacks evidence-based therapies and its underlying pathophysiological mechanisms remain incompletely understood.
Cardiometabolic HFpEF is driven by metabolic and inflammatory alterations, presenting novel therapeutic targets such as iNOS inhibition and NAD+ repletion for a disease currently lacking effective treatments.
Highlights HFpEF's ongoing clinical burden; leaves open whether cardiometabolic therapies can improve outcomes.
Heart failure with preserved ejection fraction (HFpEF) accounts for at least half of all patients with heart failure (HF) and is projected to be the most common form of HF in the near feature.HFpEF, characterized by high morbidity and mortality, poses an enormous medical and societal burden and lacks evidence-based therapies.Hence, HFpEF has been recognized as the greatest unmet need in cardiovascular medicine.HFpEF is a heterogenous syndrome presenting as several different clinical phenotypes.Among these, metabolic alterationdriven HFpEF-i.e. cardiometabolic HFpEF-is emerging around the globe as the most prevalent form of HFpEF.Pathophysiological mechanisms of cardiometabolic HFpEF are still incompletely understood.However, recent advances in the preclinical modeling of the syndrome, coupled with better definition of its clinical presentations and analysis of human HFpEF myocardial specimens, have unveiled metabolic disturbances and inflammatory burden as 2 key drivers of HFpEF pathophysiology.Here, we summarize evidence in support of a cardiometabolic phenotype of HFpEF and discuss the pivotal biological mechanisms underlying this syndrome in the hope of informing more efficacious therapeutic approaches in the future.
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Schiattarella et al. (2021) studied Heart failure with preserved ejection fraction (HFpEF). null vs. null was evaluated on 2-year rate of HF hospitalization. HFpEF has a 2-year rate of hospitalization of 35% and a 2-year mortality of 14%.
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