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. 2024 Feb 12;110(5):359-365.
doi: 10.1136/heartjnl-2023-323049.

Rationale and design of the United Kingdom Heart Failure with Preserved Ejection Fraction Registry

Collaborators
Free article

Rationale and design of the United Kingdom Heart Failure with Preserved Ejection Fraction Registry

UK HFpEF Collaborative Group. Heart. .
Free article

Abstract

Objective: Heart failure with preserved ejection fraction (HFpEF) is a common heterogeneous syndrome that remains imprecisely defined and consequently has limited treatment options and poor outcomes.

Methods: The UK Heart Failure with Preserved Ejection Fraction Registry (UK HFpEF) is a prospective data-enabled cohort and platform study. The study will develop a large, highly characterised cohort of patients with HFpEF. A biobank will be established. Deep clinical phenotyping, imaging, multiomics and centrally held national electronic health record data will be integrated at scale, in order to reclassify HFpEF into distinct subgroups, improve understanding of disease mechanisms and identify new biological pathways and molecular targets. Together, these will form the basis for developing diagnostics and targeted therapeutics specific to subgroups. It will be a platform for more effective and efficient trials, focusing on subgroups in whom targeted interventions are expected to be effective, with consent in place to facilitate rapid recruitment, and linkage for follow-up. Patients with a diagnosis of HFpEF made by a heart failure specialist, who have had natriuretic peptide levels measured and a left ventricular ejection fraction >40% are eligible. Patients with an ejection fraction between 40% and 49% will be limited to no more than 25% of the cohort.

Conclusions: UK HFpEF will develop a rich, multimodal data resource to enable the identification of disease endotypes and develop more effective diagnostic strategies, precise risk stratification and targeted therapeutics.

Trial registration number: NCT05441839.

Keywords: Heart failure with preserved ejection fraction.

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Conflict of interest statement

Competing interests: CAM has served on advisory boards for AstraZeneca, Boehringer Ingelheim and Lilly Alliance, Novartis, and PureTech Health; serves as an advisor for HAYA Therapeutics; and has received speaker fees from Boehringer Ingelheim and Novo Nordisk, conference attendance support from AstraZeneca and research support from Amicus Therapeutics, AstraZeneca, Guerbet Laboratories, Roche and Univar Solutions. RTL has received research grants from Pfizer and has provided consultancy for FITFILE and HealthLumen. SEP provides consultancy to Circle Cardiovascular Imaging, Calgary, Alberta, Canada.

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