Literature DB >> 26798687

Genes in Thoracic Aortic Aneurysms and Dissections - Do they Matter?: Translation and Integration of Research and Modern Genetic Techniques into Daily Clinical Practice.

Julie De Backer, Marjolijn Renard1, Laurence Campens, Katrien François2, Bert Callewaert1, Paul Coucke1, Anne De Paepe1.   

Abstract

Since the identification of the fibrillin-1 gene as the causal gene for Marfan syndrome, our knowledge of molecular genetics and the applicability of genetic testing in clinical practice have expanded dramatically. Several new syndromes related to thoracic aortic aneurysms and dissections (TAAD) have been described and the list of underlying genes in syndromal and nonsyndromal TAAD already includes more than 10 different genes and is rapidly expanding. Based on this knowledge, our insights into the underlying pathophysiology of TAAD have improved significantly, and new opportunities for targeted treatment have emerged. Clinicians involved in the care of TAAD patients require a basic knowledge of the disease entities and need to be informed on the applicability of genetic testing in their patients and families. Gene-tailored treatment and management is indeed no science fiction anymore and should now be considered as part of good clinical practice. We provide a systematic overview of genetic TAAD entities and practical recommendations for genetic testing and patient management.

Entities:  

Keywords:  Aneurysm syndrome; Molecular genetic testing; Thoracic aortic aneurysms and dissections

Year:  2013        PMID: 26798687      PMCID: PMC4682714          DOI: 10.12945/j.aorta.2013.13-024

Source DB:  PubMed          Journal:  Aorta (Stamford)        ISSN: 2325-4637


  59 in total

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Authors:  Sumera N Hasham; Dong-chuan Guo; Dianna M Milewicz
Journal:  Curr Opin Cardiol       Date:  2002-11       Impact factor: 2.161

2.  Phenotypic spectrum of the SMAD3-related aneurysms-osteoarthritis syndrome.

Authors:  Ingrid M B H van de Laar; Denise van der Linde; Edwin H G Oei; Pieter K Bos; Johannes H Bessems; Sita M Bierma-Zeinstra; Belle L van Meer; Gerard Pals; Rogier A Oldenburg; Jos A Bekkers; Adriaan Moelker; Bianca M de Graaf; Gabor Matyas; Ingrid M E Frohn-Mulder; Janneke Timmermans; Yvonne Hilhorst-Hofstee; Jan M Cobben; Hennie T Bruggenwirth; Lut van Laer; Bart Loeys; Julie De Backer; Paul J Coucke; Harry C Dietz; Patrick J Willems; Ben A Oostra; Anne De Paepe; Jolien W Roos-Hesselink; Aida M Bertoli-Avella; Marja W Wessels
Journal:  J Med Genet       Date:  2012-01       Impact factor: 6.318

3.  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

4.  Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene.

Authors:  H C Dietz; G R Cutting; R E Pyeritz; C L Maslen; L Y Sakai; G M Corson; E G Puffenberger; A Hamosh; E J Nanthakumar; S M Curristin
Journal:  Nature       Date:  1991-07-25       Impact factor: 49.962

5.  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

6.  Angiotensin II blockade and aortic-root dilation in Marfan's syndrome.

Authors:  Benjamin S Brooke; Jennifer P Habashi; Daniel P Judge; Nishant Patel; Bart Loeys; Harry C Dietz
Journal:  N Engl J Med       Date:  2008-06-26       Impact factor: 91.245

7.  In-frame mutations in exon 1 of SKI cause dominant Shprintzen-Goldberg syndrome.

Authors:  Virginie Carmignac; Julien Thevenon; Lesley Adès; Bert Callewaert; Sophie Julia; Christel Thauvin-Robinet; Lucie Gueneau; Jean-Benoit Courcet; Estelle Lopez; Katherine Holman; Marjolijn Renard; Henri Plauchu; Ghislaine Plessis; Julie De Backer; Anne Child; Gavin Arno; Laurence Duplomb; Patrick Callier; Bernard Aral; Pierre Vabres; Nadège Gigot; Eloisa Arbustini; Maurizia Grasso; Peter N Robinson; Cyril Goizet; Clarisse Baumann; Maja Di Rocco; Jaime Sanchez Del Pozo; Frédéric Huet; Guillaume Jondeau; Gwenaëlle Collod-Beroud; Christophe Beroud; Jeanne Amiel; Valérie Cormier-Daire; Jean-Baptiste Rivière; Catherine Boileau; Anne De Paepe; Laurence Faivre
Journal:  Am J Hum Genet       Date:  2012-10-25       Impact factor: 11.025

8.  Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome.

Authors:  Paul J Coucke; Andy Willaert; Marja W Wessels; Bert Callewaert; Nicoletta Zoppi; Julie De Backer; Joyce E Fox; Grazia M S Mancini; Marios Kambouris; Rita Gardella; Fabio Facchetti; Patrick J Willems; Ramses Forsyth; Harry C Dietz; Sergio Barlati; Marina Colombi; Bart Loeys; Anne De Paepe
Journal:  Nat Genet       Date:  2006-03-19       Impact factor: 38.330

9.  Analysis of multigenerational families with thoracic aortic aneurysms and dissections due to TGFBR1 or TGFBR2 mutations.

Authors:  V Tran-Fadulu; H Pannu; D H Kim; G W Vick; C M Lonsford; A L Lafont; C Boccalandro; S Smart; K L Peterson; J Zenger Hain; M C Willing; J S Coselli; S A LeMaire; C Ahn; P H Byers; D M Milewicz
Journal:  J Med Genet       Date:  2009-06-18       Impact factor: 6.318

10.  Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD.

Authors:  Marjolijn Renard; Bert Callewaert; Machteld Baetens; Laurence Campens; Kay MacDermot; Jean-Pierre Fryns; Maryse Bonduelle; Harry C Dietz; Isabel Mendes Gaspar; Diogo Cavaco; Eva-Lena Stattin; Constance Schrander-Stumpel; Paul Coucke; Bart Loeys; Anne De Paepe; Julie De Backer
Journal:  Int J Cardiol       Date:  2011-09-19       Impact factor: 4.164

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  2 in total

1.  Functional validation reveals the novel missense V419L variant in TGFBR2 associated with Loeys-Dietz syndrome (LDS) impairs canonical TGF-β signaling.

Authors:  Margot A Cousin; Michael T Zimmermann; Angela J Mathison; Patrick R Blackburn; Nicole J Boczek; Gavin R Oliver; Gwen A Lomberk; Raul A Urrutia; David R Deyle; Eric W Klee
Journal:  Cold Spring Harb Mol Case Stud       Date:  2017-07-05

2.  Targeted genetic analysis in a large cohort of familial and sporadic cases of aneurysm or dissection of the thoracic aorta.

Authors:  Ruwan Weerakkody; David Ross; David A Parry; Bulat Ziganshin; Jana Vandrovcova; Piyush Gampawar; Abdulshakur Abdullah; Jennifer Biggs; Julia Dumfarth; Yousef Ibrahim; Colin Bicknell; Mark Field; John Elefteriades; Nick Cheshire; Timothy J Aitman
Journal:  Genet Med       Date:  2018-03-15       Impact factor: 8.822

  2 in total

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