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Prevalence of aortic dilation in hypertrophic cardiomyopathy
Renuka Jain1, Adam Helms, Sharlene M Day
1Lillehei Heart Institute and Cardiovascular Division, University of Minnesota Medical School Minneapolis, MN, USA.
Insights
Hypertrophic cardiomyopathy (HCM) is not linked to aortic dilation. This study found no increased frequency of aortic dilation in HCM patients compared to the general population.
Area of Science:
- Cardiology
- Cardiovascular Imaging
- Genetics
Background:
- Recent research suggests hypertrophic cardiomyopathy (HCM) correlates with aortic stiffness.
- However, the relationship between HCM and aortic dilation remains unclear.
Purpose of the Study:
- To investigate the prevalence of aortic dilation in patients with hypertrophic cardiomyopathy.
- To determine if aortic dilation is associated with HCM characteristics.
Main Methods:
- Aorta size was measured in 223 HCM patients using echocardiography.
- Aortic dilation was defined using established criteria accounting for body surface area, age, and gender.
- HCM characteristics including hypertrophy pattern, maximum wall thickness, and left ventricular outflow tract (LVOT) gradient were assessed.
Main Results:
- The mean aorta size was 33.0 ± 5.0 mm at the sinuses and 34.0 ± 5.0 mm at the ascending aorta.
- Aortic dilation was observed in 4.5% of the HCM cohort.
- Aortic dilation was associated with gender but not with HCM-specific features like LVOT obstruction or hypertrophy extent.
Conclusions:
- Aortic dilation does not appear to be more frequent in HCM patients than in the general population.
- The study found no association between aortic dilation and the severity of hypertrophy or LVOT obstruction in HCM.
Abstract:
Recent studies have suggested that hypertrophic cardiomyopathy (HCM) is associated with increased stiffness of the aorta. However, a potential relationship between HCM and aortic dilation has not been established. Aorta size was characterized in 223 consecutive patients diagnosed with HCM. Aorta size was measured at the level of the sinuses (n = 223) and ascending aorta (n = 115) using the parasternal long-axis echocardiographic view. Hypertrophy pattern, maximum wall thickness, and left ventricular outflow tract gradient were measured. Aortic dilation was defined using previously published criteria that control for body surface area, age, and gender. Mean aorta size among the HCM cohort was 33.0 ± 5.0 mm at the sinuses and 34.0 ± 5.0 at the tubular aorta. Using the age-based nomogram controlling for body surface area, 10 (4.5%) of the study population had dilated aortas at the sinuses of Valsalva. Only gender (10/10 male in dilated group, 127/213 in non-dilated group, p = 0.008) was associated with dilation, while characteristics of HCM (LVOT obstruction, maximum wall thickness, hypertrophy pattern) were not. Use of other criteria for dilation did not result in an association with HCM characteristics. Aortic dilation in HCM does not seem to occur more frequently than in the general population and is not related to the extent of hypertrophy or LVOT obstruction.
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