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The Genetics of Thoracic Aortic Aneurysms and Dissection: A Clinical Perspective

Thoracic aortic aneurysm and dissection (TAAD) affects many patients globally and has high mortality rates if undetected. Once thought to be solely a degenerative disease that afflicted the aorta due to high pressure and biomechanical stress, extensive investigation of the heritability and natural h...

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Autores principales: Ostberg, Nicolai P., Zafar, Mohammad A., Ziganshin, Bulat A., Elefteriades, John A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072177/
https://www.ncbi.nlm.nih.gov/pubmed/31991693
http://dx.doi.org/10.3390/biom10020182
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author Ostberg, Nicolai P.
Zafar, Mohammad A.
Ziganshin, Bulat A.
Elefteriades, John A.
author_facet Ostberg, Nicolai P.
Zafar, Mohammad A.
Ziganshin, Bulat A.
Elefteriades, John A.
author_sort Ostberg, Nicolai P.
collection PubMed
description Thoracic aortic aneurysm and dissection (TAAD) affects many patients globally and has high mortality rates if undetected. Once thought to be solely a degenerative disease that afflicted the aorta due to high pressure and biomechanical stress, extensive investigation of the heritability and natural history of TAAD has shown a clear genetic basis for the disease. Here, we review both the cellular mechanisms and clinical manifestations of syndromic and non-syndromic TAAD. We particularly focus on genes that have been linked to dissection at diameters <5.0 cm, the current lower bound for surgical intervention. Genetic screening tests to identify patients with TAAD associated mutations that place them at high risk for dissection are also discussed.
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spelling pubmed-70721772020-03-19 The Genetics of Thoracic Aortic Aneurysms and Dissection: A Clinical Perspective Ostberg, Nicolai P. Zafar, Mohammad A. Ziganshin, Bulat A. Elefteriades, John A. Biomolecules Review Thoracic aortic aneurysm and dissection (TAAD) affects many patients globally and has high mortality rates if undetected. Once thought to be solely a degenerative disease that afflicted the aorta due to high pressure and biomechanical stress, extensive investigation of the heritability and natural history of TAAD has shown a clear genetic basis for the disease. Here, we review both the cellular mechanisms and clinical manifestations of syndromic and non-syndromic TAAD. We particularly focus on genes that have been linked to dissection at diameters <5.0 cm, the current lower bound for surgical intervention. Genetic screening tests to identify patients with TAAD associated mutations that place them at high risk for dissection are also discussed. MDPI 2020-01-24 /pmc/articles/PMC7072177/ /pubmed/31991693 http://dx.doi.org/10.3390/biom10020182 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ostberg, Nicolai P.
Zafar, Mohammad A.
Ziganshin, Bulat A.
Elefteriades, John A.
The Genetics of Thoracic Aortic Aneurysms and Dissection: A Clinical Perspective
title The Genetics of Thoracic Aortic Aneurysms and Dissection: A Clinical Perspective
title_full The Genetics of Thoracic Aortic Aneurysms and Dissection: A Clinical Perspective
title_fullStr The Genetics of Thoracic Aortic Aneurysms and Dissection: A Clinical Perspective
title_full_unstemmed The Genetics of Thoracic Aortic Aneurysms and Dissection: A Clinical Perspective
title_short The Genetics of Thoracic Aortic Aneurysms and Dissection: A Clinical Perspective
title_sort genetics of thoracic aortic aneurysms and dissection: a clinical perspective
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072177/
https://www.ncbi.nlm.nih.gov/pubmed/31991693
http://dx.doi.org/10.3390/biom10020182
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