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.

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