Heart Failure With Preserved Ejection Fraction: Is Ischemia Due to Coronary Microvascular Dysfunction a Mechanistic Factor?

Islam Y. Elgendy, Carl J. Pepine

Research output: Contribution to journalReview articlepeer-review

50 Scopus citations

Abstract

Heart failure with preserved ejection fraction (HFpEF) is increasing in prevalence and has no guideline-recommended therapy, related in part to a lack of mechanism. Traditionally, HFpEF was thought to be secondary to afterload overload due to systemic hypertension; however, accumulating evidence suggests that HFpEF continues to worsen despite adequate control of blood pressure. Emerging data support the suggestion that myocardial ischemia secondary to coronary microvascular dysfunction could be the new paradigm pathophysiology. Several prospective, observational cohort studies indicate that the outcomes of patients with microvascular dysfunction, after an interval of several years, are dominated by HFpEF hospitalizations. Further, the most prevalent clinical phenotype (eg older women with multiple comorbidities) of patients with HFpEF resembles those with coronary microvascular dysfunction, albeit older. In this review, we provide in-depth insight about this emerging HFpEF paradigm, discuss potential therapeutic implications of this pathophysiology, and summarize some important knowledge gaps.

Original languageEnglish
Pages (from-to)692-697
Number of pages6
JournalAmerican Journal of Medicine
Volume132
Issue number6
DOIs
StatePublished - Jun 2019

Bibliographical note

Publisher Copyright:
© 2019 Elsevier Inc.

Funding

Funding: CJP receives support from the National Institutes of Health (NIH), National Heart, Lung and Blood Institute HL087366; HL033610, HL132448, HL130163; the United States Department of Defense PR161603; the Gatorade Trust through funds distributed by the University of Florida Department of Medicine; NIH NCATS—University of Florida Clinical and Translational Science UL1TR001427; and PCORnet-OneFlorida Clinical Research Consortium CDRN-1501-26692.

FundersFunder number
Gatorade Trust
PCORnet-OneFlorida Clinical Research ConsortiumCDRN-1501-26692
University of Florida Department of Medicine
National Institutes of Health (NIH)
U.S. Department of DefensePR161603
National Heart, Lung, and Blood Institute (NHLBI)HL130163, HL087366, HL132448
National Center for Advancing Translational Sciences (NCATS)UL1TR001427
Clinical and Translational Science Institute, University of Florida

    Keywords

    • Coronary artery disease
    • Heart failure
    • Ischemia
    • Microvascular dysfunction
    • Preserved ejection fraction

    ASJC Scopus subject areas

    • General Medicine

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