The relationship between coronary microvascular dysfunction, atrial fibrillation and heart failure with preserved ejection fraction
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Updated: Nov 10, 2025

Estimating Bilateral Atrial Function by Cardiovascular Magnetic Resonance Feature Tracking in Patients with Paroxysmal Atrial Fibrillation
Published on: July 20, 2022
Cevher Ozcan1,2, Tess Allan3, Stephanie A Besser1,2
1Department of Medicine, University of Chicago 5841 S. Maryland Avenue, MC 6080, Chicago, IL 60637, USA.
Insights
Coronary microvascular dysfunction (CMD) is common in patients with atrial fibrillation (AF) and heart failure with preserved ejection fraction (HFpEF). This association predicts poor outcomes, highlighting the need for targeted treatment strategies.
Area of Science:
- Cardiology
- Vascular Medicine
- Electrophysiology
Background:
- Coronary microvascular dysfunction (CMD) is a significant factor in myocardial ischemia and is prevalent in heart failure.
- The relationship between CMD and atrial fibrillation (AF) remains unclear, particularly concerning co-existence with heart failure with preserved ejection fraction (HFpEF).
Purpose of the Study:
- To investigate the association between CMD, AF, and HFpEF.
- To determine if CMD increases susceptibility to the combined presence of AF and HFpEF.
- To assess the clinical outcomes associated with CMD, AF, and HFpEF.
Main Methods:
- Invasive coronary physiology studies were conducted in patients presenting with chest pain or dyspnea.
- Coronary microvascular dysfunction (CMD) was defined by impaired coronary flow reserve (CFR) in the absence of obstructive coronary artery disease.
- Patient data including presence of AF, HFpEF, and clinical outcomes were analyzed.
Main Results:
- Coronary microvascular dysfunction (CMD) was highly prevalent in patients with AF (61%) and HFpEF (62%), with 71% having both conditions.
- CMD was a significant predictor of AF with concomitant HFpEF (OR 4.38, P=0.02).
- Patients with CMD, AF, or HFpEF experienced reduced survival free of HF hospitalization; AF was a strong predictor of CMD (OR 5.5, P=0.02).
Conclusions:
- Coronary microvascular dysfunction (CMD) is highly prevalent in patients with atrial fibrillation (AF), with or without heart failure with preserved ejection fraction (HFpEF).
- CMD is linked to adverse clinical outcomes, including the co-occurrence of AF and HFpEF.
- Understanding the CMD-AF association is crucial for effective treatment strategies and risk stratification in cardiovascular disease prevention.
Objective:
Coronary microvascular dysfunction (CMD) is a new frontier in cardiovascular disease and an important contributor to myocardial ischemia. A high prevalence of CMD is shown in heart failure, however, the cause-and-effect relationship between CMD and atrial fibrillation (AF) is unknown. We hypothesize that CMD is associated with AF and increases susceptibility to the co-existence of AF and heart failure with preserved ejection fraction (HFpEF).
Methods:
Our study examined the relationship between CMD, AF, and HFpEF in all patients who underwent invasive coronary physiology studies for assessment of chest pain or dyspnea. CMD was defined as impaired coronary flow reserve (CFR) without obstructive coronary disease.
Results:
A total of 80 patients (mean age 60±12 years, 68.8% female, median follow up of 2.2 years) were studied. Patients with AF (61%) or HFpEF (62%), or both (71%) were more likely to have CMD than those patients without these conditions. Of the patients with AF and abnormal CFR, 91% had HFpEF. CMD was a predictor of AF with concomitant HFpEF (OR 4.38, P=0.02). Our clinical outcome analysis demonstrated that patients with CMD, AF or HFpEF had lower survival free of HF hospitalization than those patients without (P<0.05). AF (OR 5.5, P=0.02), diabetes, older age, female gender, and higher heart rate were predictors of CMD.
Conclusion:
CMD is highly prevalent in patients with AF with or without HFpEF. CMD is associated with poor clinical outcomes and the co-existence of AF and HFpEF. Understanding of the association between CMD and AF is important for developing an effective treatment strategy and the risk stratification for the prevention of AF in patients with CMD and vice versa.
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