Medical Therapy for Heart Failure Caused by Ischemic Heart Disease

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146 Scopus citations

Abstract

Patients with heart failure (HF) syndromes have been categorized as those with reduced ejection fraction (EF) or preserved EF (HFpEF), and ischemia plays a key role in both types. HF remains a major cause of morbidity and mortality worldwide, and with the aging of our population this burden continues to rise, predominantly as a result of hospitalizations for HFpEF. Patients with obstructive coronary artery disease more likely have HF with reduced EF, rather than HFpEF, secondary to acute ischemic injury resulting in myocardial infarction, and large outcomes trials of treatments with neurohumoral inhibition have documented reduced adverse outcomes. In contrast, similar treatments in patients with HFpEF have not proven beneficial. This therapeutic dilemma may be attributed, in part, to heterogeneity in the underlying pathophysiology with different systemic and myocardial signaling pathways, despite similar clinical presentations and findings, in patients with HFpEF. Also, emerging evidence indicates that impaired myocardial perfusion and inflammation secondary to multiple comorbidities are key mechanisms in HFpEF. We will thoroughly review the role of ischemic heart disease in the pathogenesis of HF with reduced EF and HFpEF, and discuss the medical management strategies available for these conditions.

Original languageEnglish
Pages (from-to)1520-1535
Number of pages16
JournalCirculation Research
Volume124
Issue number11
DOIs
StatePublished - May 24 2019

Bibliographical note

Publisher Copyright:
© 2019 American Heart Association, Inc.

Funding

C.J. Pepine receives support from the National Institutes of Health (NIH; HL087366, HL132448, HL033610, and HL130163); the US Department of Defense (PR161603—WARRIOR Trial [Women’s Ischemia Trial to Reduce Events in Non-Obstructive CAD]); the Gatorade Trust through funds distributed by the University of Florida Department of Medicine; NIH NCATS (National Center for Advancing Translational Sciences)—University of Florida Clinical and Translational Science UL1TR001427; and PCORnet-OneFlorida Clinical Research Consortium CDRN-1501–26692.

FundersFunder number
Gatorade Trust
NIH NCATS
US Department of DefensePR161603
University of Florida Clinical and Translational Science UL1TR001427CDRN-1501–26692
WARRIOR Trial
National Institutes of Health (NIH)HL130163, HL087366, HL132448
National Heart, Lung, and Blood Institute (NHLBI)R37HL033610
National Center for Advancing Translational Sciences (NCATS)UL1TR001427
Department of Pediatrics, University of Florida

    Keywords

    • coronary artery disease
    • heart failure
    • hospitalization
    • inflammation
    • myocardial ischemia

    ASJC Scopus subject areas

    • Physiology
    • Cardiology and Cardiovascular Medicine

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