Literature DB >> 26604122

Genetic Testing in Thoracic Aortic Disease--When, Why, and How?

Sarah C Bowdin1, Anne-Marie Laberge2, Aline Verstraeten3, Bart L Loeys4.   

Abstract

Advances in genetic technology over the past 10 years have revealed the polygenic basis of thoracic aortic aneurysm and thoracic aortic acute dissection (TAAD) in a subset of patients. There is mounting evidence to show that clinical risk stratification for aneurysmal dilatation and acute dissection can be based on genotype for some of the known genes, allowing individualized medical and surgical management with the aim of reducing morbidity and mortality. This evidence has led to a recommendation by the American College of Cardiology Foundation and the American Heart Association that the underlying genetic mutation should dictate the timing of aortic repair. Other benefits of identifying a specific genetic cause include prediction of multisystem involvement in syndromic forms of TAAD and cascade screening for other at-risk family members. Mutation analysis for genes associated with TAAD in a clinical setting is typically ordered by geneticists or cardiologists with an interest or expertise in cardiac genetics. We present an approach to assist cardiologists and vascular surgeons in recognizing which patients would benefit from genetic testing, provide justification for such testing, and outline a practical approach to ordering the tests.
Copyright © 2016 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 26604122     DOI: 10.1016/j.cjca.2015.09.018

Source DB:  PubMed          Journal:  Can J Cardiol        ISSN: 0828-282X            Impact factor:   5.223


  5 in total

1.  Postmortem genetic testing should be recommended in sudden cardiac death cases due to thoracic aortic dissection.

Authors:  Marina Gago-Díaz; Eva Ramos-Luis; Silvia Zoppis; Esther Zorio; Pilar Molina; Aitana Braza-Boïls; Juan Giner; Beatriz Sobrino; Jorge Amigo; Alejandro Blanco-Verea; Ángel Carracedo; María Brion
Journal:  Int J Legal Med       Date:  2017-04-08       Impact factor: 2.686

2.  Confirmation of the role of pathogenic SMAD6 variants in bicuspid aortic valve-related aortopathy.

Authors:  Ilse Luyckx; Gretchen MacCarrick; Marlies Kempers; Josephina Meester; Céline Geryl; Olivier Rombouts; Nils Peeters; Charlotte Claes; Nele Boeckx; Natzi Sakalihasan; Adeline Jacquinet; Alexander Hoischen; Geert Vandeweyer; Sarah Van Lent; Johan Saenen; Emeline Van Craenenbroeck; Janneke Timmermans; Anthonie Duijnhouwer; Harry Dietz; Lut Van Laer; Bart Loeys; Aline Verstraeten
Journal:  Eur J Hum Genet       Date:  2019-02-22       Impact factor: 4.246

3.  Genetic screening in heritable thoracic aortic disease-rationale, potentials and pitfalls.

Authors:  Metesh Acharya; Daniele Maselli; Giovanni Mariscalco
Journal:  Indian J Thorac Cardiovasc Surg       Date:  2021-03-02

4.  Vascular Deformation Mapping (VDM) of Thoracic Aortic Enlargement in Aneurysmal Disease and Dissection.

Authors:  Nicholas S Burris; Benjamin A Hoff; Ella A Kazerooni; Brian D Ross
Journal:  Tomography       Date:  2017-09

5.  Familial aortic disease and a large duplication in chromosome 16p13.1.

Authors:  Philipp Erhart; Tobias Brandt; Beate K Straub; Ingrid Hausser; Sabine Hentze; Dittmar Böckler; Caspar Grond-Ginsbach
Journal:  Mol Genet Genomic Med       Date:  2018-02-14       Impact factor: 2.183

  5 in total

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