Echogenomics: Echocardiography in Heritable Aortopathies

Lyndsey Hunter-Adamson,Seda Tierney

CURRENT CARDIOLOGY REPORTS(2024)

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摘要
Purpose of ReviewThe aim of this article is to review the current echocardiographic considerations in the diagnosis and monitoring of patients with inherited aortopathies.Recent FindingsAortic dilation is a key feature in heritable aortopathies, and dissection is a leading cause of morbidity and mortality. New genetic and histopathologic findings are helpful in better understanding these conditions. Non-invasive imaging modalities, including echocardiogram, computerized tomography, and magnetic resonance imaging, are essential in monitoring these patients, as well as providing new prognostic factors of arterial stiffness that may help with risk stratification in the future.SummaryDiagnosis of heritable aortopathies should be considered with identification of aortic root dilation, particularly in children and young adults, or when there is a family history of aortic disease. Recent adult consensus guidelines highlight the importance of underlying genotype and phenotypic features when considering prophylactic surgical intervention. There are currently no consensus pediatric guidelines.
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关键词
Echogenomics,Aortopathy,Echocardiography,Marfan Syndrome,Loeys Dietz Syndrome,Bicuspid Aortic Valve
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