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Coronary microvascular dysfunction, arrythmias, and sudden cardiac death: A literature review
Razan Dankar1, Jad Wehbi1, Mohamad Montaser Atasi1
1Division of Cardiology, Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
Insights
Coronary microvascular dysfunction (CMD) affects half of angina patients, increasing risks for atrial fibrillation, ventricular issues, and sudden cardiac arrest. Understanding CMD
Area of Science:
- Cardiology
- Vascular Biology
- Cardiac Electrophysiology
Background:
- The coronary vascular system's structure adapts to myocardial demand, with a network from epicardial arteries to microcirculation.
- Myocardial ischemia, resulting from unmet demand, leads to angina and adverse outcomes.
- Coronary microvascular dysfunction (CMD) is prevalent, affecting 66% of angina patients with non-obstructive coronary disease.
Purpose of the Study:
- To elucidate the impact of CMD on cardiac function and patient outcomes.
- To explore the association between CMD and conditions like atrial fibrillation and ventricular repolarization abnormalities.
- To identify the underlying pathogenesis of CMD.
Main Methods:
- Analysis of existing literature and patient data concerning coronary microvascular function.
- Review of studies linking CMD to atrial fibrillation and ventricular electrical properties.
- Examination of etiological factors including oxidative stress and structural changes.
Main Results:
- CMD is independently associated with atrial fibrillation and increased ventricular electrical inhomogeneity.
- CMD contributes to the progression of cardiac disease and increases mortality risk.
- Pathogenesis involves oxidative stress, impaired vasoactivity, and structural disorders like fibrosis.
Conclusions:
- CMD significantly impacts atrial and ventricular function, increasing risks for arrhythmias and sudden cardiac arrest.
- Distorted ventricular repolarization parameters (e.g., QT dispersion) in CMD can promote ventricular arrhythmias.
- CMD represents a critical, independent risk factor for adverse cardiovascular events and mortality.
Abstract:
The coronary vascular system has a unique structure and function that is adaptive to myocardial demand. It is composed of a continuous network of vessels receding in size from epicardial arteries to the microvascular circulation. Failure to meet myocardial demand results in ischemia, angina, and adverse myocardial outcomes. It is evident that 50 % of patients with angina have a non-obstructive coronary disease and 66 % of these patients have coronary microvascular dysfunction (CMD). The impact of CMD on the atria and ventricles is exhibited through its association with atrial fibrillation and distortion of ventricular repolarization. Ultimately, this influence increases the risk of mortality, morbidity, and sudden cardiac arrest. CMD serves as an independent risk for atrial fibrillation, increases ventricular electrical inhomogeneity, and contributes to the progression of cardiac disease. The underlying pathogenesis may be attributed to oxidative stress evident through reactive oxygen species, impaired vasoactive function, and structural disorders such as fibrotic changes. Myocardial ischemia, brought about by a demand-supply mismatch in CMD, may create a milieu for ventricular arrythmia and sudden cardiac arrest through distortion of ventricular repolarization parameters such as QT dispersion and corrected QT dispersion.
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