Literature DB >> 28555287

Genetic diagnostics of inherited aortic diseases : Medical strategy analysis.

Y von Kodolitsch1,2, K Kutsche3.   

Abstract

Genetic aortic syndromes (GAS) include Marfan, Loeys-Dietz, vascular Ehlers-Danlos, and Turner syndrome as well as congenital bicuspid aortic valve. The clinical management of these diseases has certain similarities and differences. We employed medical strategy analysis to test the utility of genetic diagnostics in the management of GAS. We chose the standpoint of the cardiologist for our analysis. In the first step, the medical goals in the management of GAS are specified. In the second step, the accuracy of genetic diagnostics for GAS is examined. Finally, conclusions can be drawn about the utility of genetic diagnostics in managing GAS. We found that genetic diagnostics is necessary to exclude GAS, to diagnose GAS, and to specify disease types. Second, combining phenotype with genotype information maximizes the predictability of the course of disease. Third, with genetic diagnostics it is possible to predict the birth of children with causative mutations for GAS and to initiate drug therapy to prevent the onset of aortic dilatation or to slow down its progression to aortic aneurysm. Finally, genetic diagnostics improves prognostic predictions and thereby contributes to a better timing of elective surgery and to a better choice of procedures. The findings of our medical strategy analysis indicate the high utility of genetic diagnostics for managing GAS.

Entities:  

Keywords:  Diagnostic techniques; Genetics; Marfan syndrome; Microfibrils; Transforming growth factor beta

Mesh:

Substances:

Year:  2017        PMID: 28555287     DOI: 10.1007/s00059-017-4577-y

Source DB:  PubMed          Journal:  Herz        ISSN: 0340-9937            Impact factor:   1.443


  69 in total

1.  Interpretation of sequence variants of the FBN1 gene: analog or digital? A commentary on decreased frequency of FBN1 missense variants in Ghent criteria-positive Marfan syndrome and characterization of novel FBN1 variants.

Authors:  Yskert von Kodolitsch; Kerstin Kutsche
Journal:  J Hum Genet       Date:  2015-07-30       Impact factor: 3.172

2.  Preimplantation genetic diagnosis for Marfan syndrome.

Authors:  Claudia Spits; Martine De Rycke; Willem Verpoest; Willy Lissens; Andre Van Steirteghem; Inge Liebaers; Karen Sermon
Journal:  Fertil Steril       Date:  2006-06-06       Impact factor: 7.329

Review 3.  Genetic basis of thoracic aortic aneurysms and dissections: focus on smooth muscle cell contractile dysfunction.

Authors:  Dianna M Milewicz; Dong-Chuan Guo; Van Tran-Fadulu; Andrea L Lafont; Christina L Papke; Sakiko Inamoto; Carrie S Kwartler; Hariyadarshi Pannu
Journal:  Annu Rev Genomics Hum Genet       Date:  2008       Impact factor: 8.929

4.  What do French patients and geneticists think about prenatal and preimplantation diagnoses in Marfan syndrome?

Authors:  F Coron; T Rousseau; G Jondeau; E Gautier; C Binquet; L Gouya; V Cusin; S Odent; Y Dulac; H Plauchu; P Collignon; M-A Delrue; B Leheup; L Joly; F Huet; J Thevenon; G Mace; C Cassini; C Thauvin-Robinet; J E Wolf; N Hanna; P Sagot; C Boileau; L Faivre
Journal:  Prenat Diagn       Date:  2012-11-13       Impact factor: 3.050

5.  2014 ESC Guidelines on the diagnosis and treatment of aortic diseases: Document covering acute and chronic aortic diseases of the thoracic and abdominal aorta of the adult. The Task Force for the Diagnosis and Treatment of Aortic Diseases of the European Society of Cardiology (ESC).

Authors:  Raimund Erbel; Victor Aboyans; Catherine Boileau; Eduardo Bossone; Roberto Di Bartolomeo; Holger Eggebrecht; Arturo Evangelista; Volkmar Falk; Herbert Frank; Oliver Gaemperli; Martin Grabenwöger; Axel Haverich; Bernard Iung; Athanasios John Manolis; Folkert Meijboom; Christoph A Nienaber; Marco Roffi; Hervé Rousseau; Udo Sechtem; Per Anton Sirnes; Regula S von Allmen; Christiaan J M Vrints
Journal:  Eur Heart J       Date:  2014-08-29       Impact factor: 29.983

6.  Preimplantation genetic diagnosis of Marfan syndrome using multiple displacement amplification.

Authors:  Belén Lledó; Jorge Ten; Francisco M Galán; Rafael Bernabeu
Journal:  Fertil Steril       Date:  2006-10       Impact factor: 7.329

Review 7.  Aortic dissection--an update.

Authors:  Debabrata Mukherjee; Kim A Eagle
Journal:  Curr Probl Cardiol       Date:  2005-06       Impact factor: 5.200

Review 8.  Economic and care considerations of Marfan syndrome.

Authors:  Carl Rudolf Blankart; Ricarda Milstein; Meike Rybczynski; Helke Schüler; Yskert von Kodolitsch
Journal:  Expert Rev Pharmacoecon Outcomes Res       Date:  2016-10-06       Impact factor: 2.217

Review 9.  Systematic review of the psychosocial aspects of living with Marfan syndrome.

Authors:  G Velvin; T Bathen; S Rand-Hendriksen; A Ø Geirdal
Journal:  Clin Genet       Date:  2014-06-04       Impact factor: 4.438

10.  Evaluating the quality of Marfan genotype-phenotype correlations in existing FBN1 databases.

Authors:  Kristian A Groth; Yskert Von Kodolitsch; Kerstin Kutsche; Mette Gaustadnes; Kasper Thorsen; Niels H Andersen; Claus H Gravholt
Journal:  Genet Med       Date:  2016-12-01       Impact factor: 8.822

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  2 in total

Review 1.  Bicuspid aortic valve and aortic coarctation in congenital heart disease-important aspects for treatment with focus on aortic vasculopathy.

Authors:  Christoph Sinning; Elvin Zengin; Rainer Kozlik-Feldmann; Stefan Blankenberg; Carsten Rickers; Yskert von Kodolitsch; Evaldas Girdauskas
Journal:  Cardiovasc Diagn Ther       Date:  2018-12

2.  Idiopathic Aneurysm of the Aortic Arch in an Infant.

Authors:  Tomislav Cvitkovic; Elena Petena; Samir Sarikouch; Lavinia Neubert; Philipp Beerbaum; Alexander Horke; Dmitry Bobylev
Journal:  Thorac Cardiovasc Surg Rep       Date:  2022-09-19
  2 in total

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