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Targeting Preclinical Diastolic Dysfunction to Prevent Heart Failure: Contemporary Insights

  • Heart Failure Prevention (W Tang, Section Editor)
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Abstract

Diastolic dysfunction encompasses both those who are asymptomatic and those who have heart failure symptoms. Preclinical diastolic dysfunction (PDD), defined as diastolic dysfunction with preserved ejection fraction (EF) without the presence of heart failure symptoms, is prevalent and may progress to heart failure with preserved EF (HFpEF). While the causative factors of HFpEF are multifactorial, targeting PDD and its associated comorbidities prior to development of symptoms can reduce development of heart failure. Diabetes, coronary artery disease, hypertension, and renal dysfunction are targets of treatment in those with diastolic dysfunction that may decrease the risk of heart failure development. This review will focus on PDD, its epidemiology, pathophysiology, comorbid conditions, and management that may prevent development of heart failure.

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Acknowledgments

Dr. Chen received Research Grants from the National Institutes of Health PO1 HL 76611, R01 HL-84155, and Scios, Inc.; Mayo Clinic has filed patents for chimeric natriuretic peptides; Mayo Clinic has licensed patents to Capricor Therapeutics and Anexon with other patents pending at the US patent office; Dr. Chen received royalties from Capricor Therapeutics, Anexon, Inc., and UpToDate and is the cofounder of Zumbro Discovery, Inc.

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Conflict of Interest

Siu-Hin Wan has no relevant conflicts. Horng Chen has grants from the National Institutes of Health, non-financial support from Mayo Clinic, others from Zumbro Discovery, and grants from Scios, Inc., outside the submitted work. In addition, Dr. Chen has a patent Capricor Therapeutics, Anexon, Inc., and UpToDate with royalties paid.

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Correspondence to Horng H. Chen.

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This article is part of the Topical Collection on Heart Failure Prevention

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Wan, SH., Chen, H.H. Targeting Preclinical Diastolic Dysfunction to Prevent Heart Failure: Contemporary Insights. Curr Cardiovasc Risk Rep 9, 40 (2015). https://doi.org/10.1007/s12170-015-0466-1

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