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Published on: October 20, 2023
Hypertrophic cardiomyopathy with aortic dilation: a novel observation
Rayan Yousefzai1, Anushree Agarwal1, M Fuad Jan1
1Aurora Cardiovascular Services, Aurora Sinai/Aurora St. Luke's Medical Centers, University of Wisconsin School of Medicine and Public Health, 2801 W. Kinnickinnic River Parkway, Ste. 840, Milwaukee, WI, USA.
This study found that 9.0% of patients with hypertrophic cardiomyopathy (HCM) also have aortic dilation. This highlights a potential link between these two cardiovascular conditions that warrants further investigation.
Area of Science:
- Cardiology
- Genetics
- Vascular Medicine
Background:
- Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disease.
- Aortic dilation is a condition that can run in families.
- Data on the prevalence of aortic dilation in HCM patients is limited.
Purpose of the Study:
- To determine the prevalence of aortic dilation in patients diagnosed with hypertrophic cardiomyopathy.
- To investigate the association between aortic dilation and HCM.
Main Methods:
- Observational retrospective study.
- Included 201 patients referred to an HCM center between January 2011 and March 2014.
- Aortic dilation defined using American Society of Echocardiography and European Association of Cardiovascular Imaging guidelines.
Main Results:
- 18 out of 201 (9.0%) HCM patients met the criteria for aortic dilation.
- Patients with aortic dilation were more likely to be male, less likely to be hypertensive, and had larger left ventricle diameter and more aortic valve regurgitation.
- Mean ascending aorta diameter was 4.0 cm in males and 3.8 cm in females; mean sinuses of Valsalva diameter was 4.2 cm in males and 3.8 cm in females.
Conclusions:
- A novel observation of 9.0% prevalence of aortic dilation in HCM patients is reported.
- Further research is needed to understand the genetic and pathophysiological basis of this association.
- Clinical implications of aortic dilation in HCM patients require further study in larger cohorts.
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