The role of coronary microcirculation in heart failure with preserved ejection fraction: An unceasing odyssey

Kyriakos Dimitriadis1, Panagiotis Theofilis2, Georgios Koutsopoulos2

  • 1First Department of Cardiology, School of Medicine, National and Kapodistrian University of Athens, Hippokration General Hospital, Vasilissis Sofias 114, 11528, Athens, PO, Greece. dimitriadiskyr@yahoo.gr.

Heart Failure Reviews
|October 2, 2024
PubMed

Insights

Coronary microvascular dysfunction (CMD) is a key factor in heart failure with preserved ejection fraction (HFpEF). Diagnosing and treating CMD may improve outcomes for HFpEF patients.

Area of Science:

  • Cardiology
  • Cardiovascular Research

Background:

  • Heart failure with preserved ejection fraction (HFpEF) has complex causes.
  • Coronary microvascular dysfunction (CMD) is increasingly recognized as a significant contributor to HFpEF.
  • CMD involves impaired vasoreactivity, capillary loss, and inflammation.

Purpose of the Study:

  • To explore the role of coronary microvascular dysfunction (CMD) in heart failure with preserved ejection fraction (HFpEF).
  • To review diagnostic methods for CMD in HFpEF patients.
  • To discuss potential therapeutic strategies for CMD in HFpEF.

Main Methods:

  • Review of noninvasive diagnostic techniques for CMD, including echocardiography, cardiac MRI, and PET.
  • Inclusion of invasive assessment methods like coronary flow reserve and index of microcirculatory resistance.
  • Analysis of existing literature on the association between CMD and HFpEF prognosis and treatment.

Main Results:

  • CMD is frequently observed in patients with HFpEF.
  • The presence of both CMD and HFpEF is linked to a worse prognosis.
  • Limited evidence suggests potential benefits from renin-angiotensin-aldosterone system inhibitors, ranolazine, and SGLT2 inhibitors for CMD.

Conclusions:

  • CMD is a critical pathophysiological component of HFpEF.
  • Accurate diagnosis of CMD is essential for managing HFpEF.
  • Further research is needed to establish effective pharmacotherapies for CMD, including anti-inflammatory agents.

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