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Updated: May 4, 2026

Impact of Intracardiac Neurons on Cardiac Electrophysiology and Arrhythmogenesis in an Ex Vivo Langendorff System
Published on: May 22, 2018
Neurologic complications of cardiomyopathies and other myocardial disorders
1Division of Cardiology, Loyola University Medical Center, Maywood, IL, USA.
Insights
Cardiomyopathies can lead to myocardial dysfunction and increase stroke risk, particularly from atrial fibrillation. Anticoagulation therapy can reduce thrombotic events, but risks must be carefully evaluated.
Area of Science:
- Cardiology
- Neurology
- Genetics
Background:
- Cardiomyopathies, stemming from diverse causes like infections and genetic factors, frequently lead to myocardial dysfunction and congestive heart failure.
- A significant link exists between heart disease, specifically myocardial dysfunction, and neurological complications, primarily embolic stroke.
- Reduced left ventricular ejection fraction and mural thrombus formation are key indicators associated with increased embolic stroke risk.
Purpose of the Study:
- To explore the relationship between cardiomyopathies, myocardial dysfunction, and the incidence of embolic strokes.
- To highlight the role of atrial fibrillation as a primary source of thrombi and its impact on stroke risk.
- To discuss the implications of patent foramen ovale in cryptogenic strokes and the utility of anticoagulation.
Main Methods:
- Review of existing literature on cardiomyopathies, myocardial dysfunction, and cerebrovascular events.
- Analysis of the association between left ventricular ejection fraction, mural thrombus, and embolic stroke prevalence.
- Examination of the contribution of atrial fibrillation and patent foramen ovale to stroke risk.
Main Results:
- Left ventricular dysfunction in cardiomyopathies is linked to mural thrombi, with embolic stroke prevalence ranging from 3% to 50%.
- Atrial fibrillation, especially nonvalvular, significantly elevates stroke risk (4-7 times higher than normal sinus rhythm).
- Clinically silent cerebral infarctions are detectable in dilated cardiomyopathy patients via advanced imaging.
Conclusions:
- Myocardial dysfunction from cardiomyopathies necessitates careful evaluation for embolic stroke risk, with atrial fibrillation being a major contributor.
- Anticoagulation is crucial for reducing thrombotic events but requires risk-benefit assessment using validated scores.
- Genetic factors are increasingly important in understanding dilated cardiomyopathies, underscoring the need for thorough clinical assessment.
Abstract:
Cardiomyopathies have a variety of causes: infectious, genetic, valvular heart disease, coronary artery disease, hypertension, and tachycardias. All can result in myocardial dysfunction and often congestive heart failure. The main interaction between a diagnosis of heart disease and the brain is via embolic stroke. The focus here is on myocardial dysfunction. Thrombus is associated with myocardial dysfunction and depressed left ventricular ejection fractions. Reduced left ventricular ejection fractions and mural thrombus are associated with embolic strokes. Atrial fibrillation is a primary source of thrombi. Anticoagulation can significantly reduce the incidence of thrombotic problems. Patent foramen ovale has created interest in those patients with cryptogenic strokes. Cryptogenic strokes are associated with patent foramen ovales, although not all cryptogenic strokes are associated with paradoxical emboli. Clinically silent cerebral infarctions occur in patients with dilated cardiomyopathy as detected by multidetector computed tomography or magnetic resonance imaging studies. Left ventricular dysfunction from cardiomyopathies is associated with mural thrombi, but the prevalence of embolic stroke varies widely from 3% to 50%; as many as half of embolic strokes are related to atrial fibrillation. Nonvalvular atrial fibrillation can increase the risk of stroke by a factor four to seven times when compared to normal sinus rhythm. Stroke risks and bleeding risks with anticoagulation can be estimated by scores. Genetic abnormalities are increasing in importance in helping to find the etiology and inheritance of some dilated cardiomyopathies. Careful clinical evaluation remains important.
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