Myocardial ischemia in asymptomatic adults with repaired aortic coarctation

Stephen C Cook1, Amy K Ferketich, Subha V Raman

  • 1The Adolescent and Young Adult Congenital Heart Disease Program, Ohio State University, Columbus, OH 43210, United States.

Insights

Repaired coarctation of the aorta in young adults is linked to impaired myocardial perfusion reserve, even without coronary artery disease. These findings may explain long-term cardiac issues in this population.

Area of Science:

  • Cardiology
  • Cardiovascular Imaging
  • Medical Diagnostics

Background:

  • Coarctation of the aorta (CoA) is a congenital heart defect leading to hypertension and reduced survival, even after surgical repair.
  • Coronary artery disease (CAD) accounts for a significant portion of deaths in adults with repaired CoA, but the underlying cause remains unclear.
  • Previous studies lacked prospective data to identify the substrate for cardiac events in repaired CoA patients.

Purpose of the Study:

  • To investigate myocardial perfusion abnormalities in asymptomatic adults with repaired CoA using coronary computed tomography angiography (CTA) and cardiac magnetic resonance (CMR).
  • To determine if perfusion deficits exist in the absence of obstructive coronary artery disease in this population.

Main Methods:

  • Prospective enrollment of 27 repaired CoA patients and 10 matched controls.
  • Coronary CTA and CMR imaging were performed on all participants.
  • Myocardial perfusion reserve index (MPRI) was quantified by assessing myocardial signal enhancement during vasodilator stress and rest.

Main Results:

  • No patients exhibited coronary artery atherosclerosis.
  • Significantly impaired endocardial to epicardial perfusion reserve ratio was observed in repaired CoA patients compared to controls (0.72±0.16 vs. 0.91±0.08, p<0.0001).
  • This perfusion deficit remained significant even after excluding patients with recoarctation (p=0.00013).

Conclusions:

  • Adolescent and young adult patients with repaired coarctation of the aorta demonstrate abnormal myocardial perfusion reserve.
  • These perfusion abnormalities occur independently of coronary artery disease.
  • These novel in vivo findings may elucidate the mechanisms behind late-onset cardiac morbidity in repaired CoA patients.
Abstract

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