Literature DB >> 35463717

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

Metesh Acharya1, Daniele Maselli2, Giovanni Mariscalco1.   

Abstract

Thoracic aortic aneurysms are silent yet deadly clinical entities which may elude detection until an acutely life-threatening aortic dissection or rupture occurs. Approximately 20% of patients with thoracic aortic aneurysms or dissection have a positive family history, indicating a strong genetic component to the aetiology. Genetic screening in such hereditary thoracic aortic disease (HTAD) may thus be beneficial in detecting causative genetic mutations in affected patients, identifying asymptomatic family members who may be at risk, and in guiding the optimal timing of preventative surgery in those with confirmed genetic aortopathy. Genetic screening can facilitate personalised aortic care tailored to an individual's specific genetic abnormality, with the aim of mitigating the significant morbidity burden and premature mortality associated with HTAD. This review examines the rationale for genetic screening in HTAD, its potential applications, current limitations and potential future directions. © Indian Association of Cardiovascular-Thoracic Surgeons 2021.

Entities:  

Keywords:  Genetic testing; Non-syndromic thoracic aortic aneurysm; Screening; Syndromic thoracic aortic aneurysm; Thoracic aortic disease

Year:  2021        PMID: 35463717      PMCID: PMC8980988          DOI: 10.1007/s12055-020-01124-7

Source DB:  PubMed          Journal:  Indian J Thorac Cardiovasc Surg        ISSN: 0970-9134


  59 in total

1.  A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.

Authors:  Bart L Loeys; Junji Chen; Enid R Neptune; Daniel P Judge; Megan Podowski; Tammy Holm; Jennifer Meyers; Carmen C Leitch; Nicholas Katsanis; Neda Sharifi; F Lauren Xu; Loretha A Myers; Philip J Spevak; Duke E Cameron; Julie De Backer; Jan Hellemans; Yan Chen; Elaine C Davis; Catherine L Webb; Wolfram Kress; Paul Coucke; Daniel B Rifkin; Anne M De Paepe; Harry C Dietz
Journal:  Nat Genet       Date:  2005-01-30       Impact factor: 38.330

2.  Do Familial Aortic Dissections Tend to Occur at the Same Age?

Authors:  Alan S Chou; Wei-Guo Ma; Salvior C M Mok; Bulat A Ziganshin; Sven Peterss; John A Rizzo; Maryann Tranquilli; John A Elefteriades
Journal:  Ann Thorac Surg       Date:  2016-08-25       Impact factor: 4.330

Review 3.  Thoracic aortic aneurysm clinically pertinent controversies and uncertainties.

Authors:  John A Elefteriades; Emily A Farkas
Journal:  J Am Coll Cardiol       Date:  2010-03-02       Impact factor: 24.094

4.  Aneurysm syndromes caused by mutations in the TGF-beta receptor.

Authors:  Bart L Loeys; Ulrike Schwarze; Tammy Holm; Bert L Callewaert; George H Thomas; Hariyadarshi Pannu; Julie F De Backer; Gretchen L Oswald; Sofie Symoens; Sylvie Manouvrier; Amy E Roberts; Francesca Faravelli; M Alba Greco; Reed E Pyeritz; Dianna M Milewicz; Paul J Coucke; Duke E Cameron; Alan C Braverman; Peter H Byers; Anne M De Paepe; Harry C Dietz
Journal:  N Engl J Med       Date:  2006-08-24       Impact factor: 91.245

5.  Reduced penetrance and variable expressivity of familial thoracic aortic aneurysms/dissections.

Authors:  D M Milewicz; H Chen; E S Park; E M Petty; H Zaghi; G Shashidhar; M Willing; V Patel
Journal:  Am J Cardiol       Date:  1998-08-15       Impact factor: 2.778

6.  Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection.

Authors:  Marjolijn Renard; Catherine Francis; Rajarshi Ghosh; Alan F Scott; P Dane Witmer; Lesley C Adès; Gregor U Andelfinger; Pauline Arnaud; Catherine Boileau; Bert L Callewaert; Dongchuan Guo; Nadine Hanna; Mark E Lindsay; Hiroko Morisaki; Takayuki Morisaki; Nicholas Pachter; Leema Robert; Lut Van Laer; Harry C Dietz; Bart L Loeys; Dianna M Milewicz; Julie De Backer
Journal:  J Am Coll Cardiol       Date:  2018-08-07       Impact factor: 24.094

7.  Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 gene.

Authors:  Chantal Stheneur; Gwenaëlle Collod-Béroud; Laurence Faivre; Jean François Buyck; Laurent Gouya; Jean-Marie Le Parc; Bertrand Moura; Christine Muti; Bernard Grandchamp; Gilles Sultan; Mireille Claustres; Philippe Aegerter; Bertrand Chevallier; Guillaume Jondeau; Catherine Boileau
Journal:  Eur J Hum Genet       Date:  2009-03-18       Impact factor: 4.246

8.  Disclosure of cardiac variants of uncertain significance results in an exome cohort.

Authors:  T A Lawal; K L Lewis; J J Johnston; A R Heidlebaugh; D Ng; F G Gaston-Johansson; W M P Klein; B B Biesecker; L G Biesecker
Journal:  Clin Genet       Date:  2018-03-02       Impact factor: 4.438

Review 9.  New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissections.

Authors:  Laurence Campens; Marjolijn Renard; Bert Callewaert; Paul Coucke; Julie De Backer; Anne De Paepe
Journal:  Pol Arch Med Wewn       Date:  2013-12-16

Review 10.  The Genetics of Aortopathies in Clinical Cardiology.

Authors:  Amit Goyal; Ali R Keramati; Matthew J Czarny; Jon R Resar; Arya Mani
Journal:  Clin Med Insights Cardiol       Date:  2017-05-30
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.