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Review Article

Arrhythmias and Coronary Slow Flow: A Potential Pathogenic Link

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DOI:

10.3791/71474

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May 29th, 2026

In This Article

Summary

This review summarizes Coronary Slow Flow (CSF) as a multifactorial syndrome associated with microvascular dysfunction, inflammation, and arrhythmias, highlighting the need for further research into its mechanisms and therapeutic strategies.

Abstract

Coronary slow flow (CSF) is characterized by recurrent resting angina and delayed distal vessel filling, despite the absence of obstructive coronary artery disease on angiography. With the continuous advancement of coronary interventional techniques, cardiologists have increasingly recognized CSF as a distinct phenomenon, and its pathogenesis has become a major research focus. Arrhythmias, common cardiovascular conditions, often present with clinical manifestations similar to those of CSF. Moreover, both conditions share certain pathogenic factors and pathophysiological processes, including endothelial dysfunction, inflammation, autonomic imbalance, and microvascular abnormalities. A clearer understanding of these overlapping mechanisms may help clinicians manage patients with CSF more scientifically and comprehensively. The present review summarizes the proposed pathogenic mechanisms of CSF, including microvascular disorders, endothelial dysfunction, inflammation, arrhythmias, anatomical factors, early atherosclerosis, and genetic polymorphisms. It also discusses the possible association between CSF and arrhythmias, highlights current uncertainties regarding causality, and considers how these mechanisms may broaden future therapeutic perspectives for this disease.

Introduction

The incidence of coronary slow flow (CSF) in patients undergoing coronary angiography (CAG) is reportedly between 1% and 7%1,2,3, a range possibly related to differences in the definition of CSF, study populations, diagnostic criteria, and geographic setting. Clinically, CSF often manifests as precordial discomfort, chest tightness, chest pain, panic, and fatigue—symptoms that are difficult to promptly distinguish from other cardiac conditions and may be associated with poor clinical prognosis. Studies have shown that CSF is associated with adverse cardiovascular events....

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Review and Perspective

Diagnostic
The current diagnostic criteria for coronary slow flow (CSF) are generally described as follows: (1) the presence of at least one non-diseased coronary vessel (i.e., coronary stenosis <40% on angiography); (2) delayed distal contrast filling; and (3) a Thrombolysis in Myocardial Infarction (TIMI) flow grade of 2 or a corrected TIMI frame count (CTFC) >27 frames (at a standard acquisition rate of 30 frames per second), after excluding secondary causes of slow flow, including coronary vasospasm, coronary embolism, coronary artery ectasia, and exogenous vasoconstrictor agents24,

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Conclusions

In recent years, coronary microvascular disorders such as CSF have gained increasing clinical attention. The strongest evidence linking arrhythmias to CSF comes from studies demonstrating that patients with atrial fibrillation (AF) have significantly higher corrected TIMI frame counts and that specific arrhythmic features, such as apical premature beats and prolonged QT dispersion, are associated with reduced coronary flow. Furthermore, systemic inflammation—a central driver of cardiovascular pathophysiology—has emerged .......

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Disclosures

The authors have no conflicts of interest to declare.

Acknowledgements

The researchers wish to express their gratitude to their colleagues at the School of Clinical Medicine of Shandong Second Medical University and the First People's Hospital of Jining City, China. We acknowledge the use of Grammarly [https://grammarly.com] to grammar-check the manuscript at the final stage of preparation. This work did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

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Tags

Cardiac ArrhythmiasEndothelial DysfunctionMicrovascular AbnormalitiesResting AnginaInflammation MechanismsAutonomic ImbalanceEarly AtherosclerosisGenetic PolymorphismsPathogenic Mechanisms