A Novel Human Biospecimen Repository for Clinical and Molecular Investigation of Thoracic Aortopathy
Thoracic aortic aneurysm (TAA) is a heritable aortopathy with significant morbidity and mortality, affecting children and adults. Genetic causes, pathobiological mechanisms, and prognostic markers are incompletely understood. In 2015, the Collaborative Human Aortopathy Repository (CHAR) was created...
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Veröffentlicht in: | Cardiogenetics 2021-09, Vol.11 (3), p.148-163 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Thoracic aortic aneurysm (TAA) is a heritable aortopathy with significant morbidity and mortality, affecting children and adults. Genetic causes, pathobiological mechanisms, and prognostic markers are incompletely understood. In 2015, the Collaborative Human Aortopathy Repository (CHAR) was created to address these fundamental gaps. Patients with thoracic aortopathy, associated genetic diagnoses, or aortic valve disease are eligible for prospective enrollment. Family members and controls are also enrolled. Detailed clinical and family data are collected, and blood and aortic tissue biospecimens are processed for broad usage. A total of 1047 participants were enrolled. The mean age in 834 affected participants was 47 ± 22 (range |
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ISSN: | 2035-8253 2035-8148 2035-8148 |
DOI: | 10.3390/cardiogenetics11030017 |