Prevalence of cardiovascular manifestations in patients with hypermobile Ehlers‐Danlos syndrome at the University of Miami

Author:

Pietri‐Toro Jariselle M.1,Gardner Olivia K.2,Leuchter Jessica D.2,DiBartolomeo Gabrielle2,Hunter Juanita A.12,Forghani Irman3ORCID

Affiliation:

1. Department of Pediatrics Holtz Children's Hospital/Jackson Health System Miami Florida USA

2. Miller School of Medicine University of Miami Coral Gables Florida USA

3. Miller School of Medicine, Department of Human Genetics University of Miami Coral Gables Florida USA

Abstract

AbstractCardiovascular system involvements have been frequently reported in hypermobile Ehlers‐Danlos Syndrome (hEDS). Mitral valve prolapse (MVP) and aortic root dilatation are included in the 2017 international classification criteria for hEDS. Different studies have found conflicting results regarding the significance of cardiac involvement in hEDS patients. We conducted a retrospective review of cardiac involvement in patients diagnosed with hEDS based on the 2017 International diagnostic criteria to provide further evidence toward more defined and reliable diagnostic criteria and recommended cardiac surveillance. A total of 75 hEDS patients with at least one diagnostic cardiac evaluation were included in the study. The most common reported cardiovascular complaints were lightheadedness (80.6%), followed by palpitations (77.6%), fainting (44.8%), and chest pain (32.8%). Of the 62 echocardiogram reports, 57 (91.9%) showed trace/trivial to mild valvular insufficiency, and 13 (21%) had additional abnormalities such as grade I diastolic dysfunction, mild aortic sclerosis, and trivial or small pericardial effusion. Of the 60 electrocardiograms (ECG) reports, 39 (65%) were normal, and 21 (35%) reported minor abnormalities or normal variants. Even though many hEDS patients in our cohort experienced cardiac symptoms, the presence of a significant cardiac abnormality was very low.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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