Prevalence of Coronary Artery Disease and Coronary Microvascular Dysfunction in Patients With Heart Failure With

Christopher J Rush1,2, Colin Berry1,2, Keith G Oldroyd1,2

  • 1British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom.

JAMA Cardiology
|June 23, 2021
PubMed

Insights

Coronary artery disease (CAD) and coronary microvascular dysfunction (CMD) are highly prevalent in heart failure with preserved ejection fraction (HFpEF) patients, often unrecognized. These conditions may represent key therapeutic targets for improving HFpEF outcomes.

Area of Science:

  • Cardiology
  • Heart Failure Research
  • Vascular Biology

Background:

  • Coronary artery disease (CAD) and coronary microvascular dysfunction (CMD) are implicated in heart failure with preserved ejection fraction (HFpEF).
  • The prevalence of CAD and CMD in HFpEF patients remains understudied.

Purpose of the Study:

  • To determine the prevalence of obstructive epicardial CAD and CMD in hospitalized patients diagnosed with HFpEF.
  • To investigate the association between these conditions and clinical outcomes.

Main Methods:

  • Prospective, multicenter cohort study of 106 HFpEF patients.
  • Coronary angiography with fractional flow reserve and coronary flow reserve assessment.
  • Cardiac magnetic resonance imaging for myocardial perfusion and fibrosis evaluation.

Main Results:

  • Obstructive epicardial CAD was found in 51% of patients; 50% of these had no prior CAD diagnosis.
  • Coronary microvascular dysfunction (CMD) was present in 66% (endothelium-independent) and 24% (endothelium-dependent).
  • 81% of patients without obstructive CAD had CMD, and 91% of all patients had evidence of either CAD, CMD, or both.

Conclusions:

  • Obstructive epicardial CAD and CMD are highly prevalent and frequently undiagnosed in hospitalized HFpEF patients.
  • CMD is common even in the absence of obstructive epicardial CAD.
  • These findings suggest that CAD and CMD are significant contributors to HFpEF pathophysiology and potential therapeutic targets.
Abstract

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