Myocardial perfusion reserve and peripheral endothelial function in patients with idiopathic dilated cardiomyopathy

Kira Q Stolen1, Jukka Kemppainen, Kari K Kalliokoski

  • 1Turku PET Centre, Turku, Finland.

Insights

Patients with idiopathic dilated cardiomyopathy (IDC) show impaired myocardial perfusion reserve, but their peripheral endothelial function remains normal. Peripheral endothelial function and heart function do not correlate in IDC patients.

Area of Science:

  • Cardiology
  • Vascular Biology
  • Medical Imaging

Background:

  • Idiopathic dilated cardiomyopathy (IDC) is a common cause of heart failure.
  • Peripheral endothelial dysfunction is often observed in heart failure patients.
  • The relationship between peripheral endothelial function and myocardial perfusion reserve in mild IDC is not well understood.

Purpose of the Study:

  • To investigate the association between peripheral endothelial function and myocardial perfusion reserve in patients with mild IDC.
  • To compare these parameters between IDC patients and healthy controls.

Main Methods:

  • Positron emission tomography (PET) with oxygen-15-labeled water was used to measure myocardial perfusion at rest and during pharmacologic hyperemia (dipyridamole).
  • Perfusion reserve was calculated as the ratio of hyperemic to resting perfusion.
  • Brachial artery flow-mediated dilation (FMD) was assessed to evaluate peripheral endothelial function.

Main Results:

  • Patients with IDC exhibited significantly lower hyperemic myocardial perfusion and perfusion reserve compared to healthy subjects.
  • Brachial artery FMD was comparable between IDC patients and healthy controls.
  • No correlation was found between FMD and myocardial perfusion reserve in IDC patients, unlike in healthy subjects.

Conclusions:

  • Abnormal myocardial perfusion reserve is a characteristic finding in patients with mild IDC.
  • Peripheral endothelial function and myocardial perfusion reserve do not run in parallel in patients with IDC.
  • These findings suggest distinct pathophysiological mechanisms affecting central and peripheral vasculature in IDC.