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Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection
- Source :
- JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, Journal of the American College of Cardiology
- Publication Year :
- 2018
- Publisher :
- Elsevier BV, 2018.
-
Abstract
- BACKGROUND Thoracic aortic aneurysms progressively enlarge and predispose to acute aortic dissections. Up to 25% of individuals with thoracic aortic disease harbor an underlying Mendelian pathogenic variant. An evidence-based strategy for selection of genes to test in hereditary thoracic aortic aneurysm and dissection (HTAAD) helps inform family screening and intervention to prevent life-threatening thoracic aortic events. OBJECTIVES The purpose of this study was to accurately identify genes that predispose to HTAAD using the Clinical Genome Resource (ClinGen) framework. METHODS We applied the semiquantitative ClinGen framework to assess presumed gene-disease relationships between 53 candidate genes and HTAAD. Genes were classified as causative for HTAAD if they were associated with isolated thoracic aortic disease and were clinically actionable, triggering routine aortic surveillance, intervention, and family cascade screening, All gene-disease assertions were evaluated by a pre-defined curator-expert pair and subsequently discussed with an expert panel. RESULTS Genes were classified based on the strength of association with HTAAD into 5 categories: definitive (n = 9), strong (n = 2), moderate (n = 4), limited (n = 15), and no reported evidence (n = 23). They were further categorized by severity of associated aortic disease and risk of progression. Eleven genes in the definitive and strong groups were designated as "HTAAD genes" (category A). Eight genes were classified as unlikely to be progressive (category B) and 4 as low risk (category C). The remaining genes were recent genes with an uncertain classification or genes with no evidence of association with HTAAD. CONCLUSIONS The ClinGen framework is useful to semiquantitatively assess the strength of gene-disease relationships for HTAAD. Gene categories resulting from the curation may inform clinical laboratories in the development, interpretation, and subsequent clinical implications of genetic testing for patients with aortic disease, (C) 2018 the American College of Cardiology Foundation, Published by Elsevier. Alt rights reserved.
- Subjects :
- ClinGen
0301 basic medicine
Candidate gene
medicine.medical_specialty
DILATION
ARTERIAL ANEURYSMS
FEATURES
thoracic aortic aneurysm
thoracic aortic dissection
Disease
030204 cardiovascular system & hematology
gene curation
Thoracic aortic aneurysm
Genome
Article
DISEASE
03 medical and health sciences
symbols.namesake
0302 clinical medicine
Internal medicine
OF-FUNCTION MUTATIONS
Medicine and Health Sciences
medicine
Humans
gene disease relationship
Gene
SYNDROME TYPE-IV
Genetic testing
Aortic Aneurysm, Thoracic
medicine.diagnostic_test
business.industry
GENOME RESOURCE
DEFECTS
medicine.disease
Aortic Dissection
Phenotype
030104 developmental biology
Clinical validity
Mendelian inheritance
symbols
Human medicine
Cardiology and Cardiovascular Medicine
business
Subjects
Details
- ISSN :
- 07351097
- Volume :
- 72
- Database :
- OpenAIRE
- Journal :
- Journal of the American College of Cardiology
- Accession number :
- edsair.doi.dedup.....8677369fbf1f82df433f5fdab96b3a6b
- Full Text :
- https://doi.org/10.1016/j.jacc.2018.04.089