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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.
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.
Abstract:
Heart failure with preserved ejection fraction (HFpEF) represents an entity with complex pathophysiologic pathways, among which coronary microvascular dysfunction (CMD) is believed to be an important orchestrator. Research in the field of CMD has highlighted impaired vasoreactivity, capillary rarefaction, and inflammation as potential mediators of its development. CMD can be diagnosed via several noninvasive methods including transthoracic echocardiography, cardiac magnetic resonance, and positron emission tomography. Moreover, invasive methods such as coronary flow reserve and index of microcirculatory resistance are commonly employed in the assessment of CMD. As far as the association between CMD and HFpEF is concerned, numerous studies have highlighted the coexistence of CMD in the majority of HFpEF patients. Additionally, patients affected by both conditions may be facing an adverse prognosis. Finally, there is limited evidence suggesting a beneficial effect of renin-angiotensin-aldosterone system blockers, ranolazine, and sodium-glucose cotransporter-2 inhibitors in CMD, with further evidence being awaited regarding the impact of other pharmacotherapies such as anti-inflammatory agents.
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