Prevalence and Clinical Correlates of Aortic Dilation in Hypertrophic Cardiomyopathy

Jeffrey B Geske1, Benjamin D Nordhues1, Nicholas M Orme2

  • 1Department of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota.

Insights

Aortic dilation is common in hypertrophic cardiomyopathy (HCM), affecting 18% of patients. Systemic hypertension is a key factor associated with this aortic enlargement, warranting further investigation into its clinical impact.

Area of Science:

  • Cardiology
  • Cardiovascular Imaging
  • Aortic Diseases

Background:

  • Aortic dilation is linked to cardiac conditions, but its prevalence and correlates in hypertrophic cardiomyopathy (HCM) are not well-defined.
  • Understanding aortic dilation in HCM is crucial for risk stratification and management.

Purpose of the Study:

  • To determine the prevalence of ascending aortic dilation in a large HCM patient cohort.
  • To identify clinical and echocardiographic factors associated with aortic dilation in HCM.

Main Methods:

  • Echocardiographic measurements of the ascending aorta in 1,698 HCM patients.
  • Aortic dilation defined by indexed dimensions (>19 mm/m²) and adjusted norms.
  • Correlation analysis between aortic size and clinical/echocardiographic parameters.

Main Results:

  • 18% of HCM patients (303/1698) had tubular ascending aortic dilation >19 mm/m².
  • Systemic hypertension was significantly associated with aortic enlargement (24.1% vs 10.5%).
  • Obstructive physiology and paroxysmal atrial fibrillation were also linked to aortic dilation.

Conclusions:

  • Aortic dilation is a frequent finding in hypertrophic cardiomyopathy.
  • Systemic hypertension is a primary correlate of aortic dilation in HCM.
  • Further research is needed to understand the clinical implications of aortic dilation in HCM patients.
Abstract

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