Literature DB >> 23176764

FBN1 gene mutation characteristics and clinical features for the prediction of mitral valve disease progression.

Kristin Kühne1, Britta Keyser, Eike F Groene, Sara Sheikhzadeh, Christian Detter, Viktoria Lorenzen, Mathias Hillebrand, Alexander M J Bernhardt, Boris Hoffmann, Thomas S Mir, Peter N Robinson, Jürgen Berger, Hermann Reichenspurner, Yskert von Kodolitsch, Meike Rybczynski.   

Abstract

BACKGROUND: Until today, FBN1 gene mutation characteristics were not compared with clinical features for the prediction of mitral valve disease progression.
METHODS: Therefore, we conducted a study of 116 patients (53 men, 63 women aged 33 ± 15 years) with a causative FBN1 gene mutation and ≤ moderate mitral valve regurgitation at baseline.
RESULTS: During 7.4 ± 6.8 years 30 patients developed progression of mitral valve regurgitation ≥ 1 grade (primary endpoint), and 26 patients required mitral valve surgery (secondary endpoint). Cox regression analysis identified an association of atrial fibrillation (hazard ratio (HR)=2.703; 95% confidence interval (CI) 1.013-7.211; P=.047), left ventricular ejection fraction (HR=.970; 95%CI .944-.997; P=.032), indexed end-diastolic left ventricular diameter (HR=15.165; 95%CI 4.498-51.128; P<.001), indexed left atrial diameter (HR=1.107; 95%CI 1.045-1.173; P=.001), tricuspid valve prolapse (HR=2.599; 95%CI 1.243-5.437; P=.011), posterior leaflet prolapse (HR=1.075; 95%CI 1.023-1.130; P=.009), and posterior leaflet thickening (HR=3.368; 95%CI 1.265-8.968; P=.015) with progression of mitral valve disease, whereas none of the FBN1 gene mutation characteristics were associated with progression of mitral valve disease. However, Cox regression analysis identified a marginal relationship of FBN1 gene mutations located both in a transforming-growth-factor beta-binding protein-like (TGFb-BP) domain (HR=3.453; 95%CI .982-12.143; P=.053), and in the calcium-binding epidermal growth factor-like (cbEGF) domain (HR=2.909; 95%CI .957-8.848; P=.060) with mitral valve surgery, a finding that was corroborated by Kaplan-Meier analysis (P=.014; and P=.041, respectively).
CONCLUSION: Clinical features were better predictors of mitral valve disease progression than FBN1 gene mutation characteristics.
Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  FBN1; Genotype; Marfan syndrome; Mitral valve prolapse; Prediction

Mesh:

Substances:

Year:  2012        PMID: 23176764     DOI: 10.1016/j.ijcard.2012.10.044

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  8 in total

Review 1.  Cardiovascular Management of Adults with Marfan Syndrome.

Authors:  Yukiko Isekame; Sabiha Gati; Jose Antonio Aragon-Martin; Rachel Bastiaenen; Sreenivasa Rao Kondapally Seshasai; Anne Child
Journal:  Eur Cardiol       Date:  2016-12

Review 2.  Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome.

Authors:  Yskert von Kodolitsch; Julie De Backer; Helke Schüler; Peter Bannas; Cyrus Behzadi; Alexander M Bernhardt; Mathias Hillebrand; Bettina Fuisting; Sara Sheikhzadeh; Meike Rybczynski; Tilo Kölbel; Klaus Püschel; Stefan Blankenberg; Peter N Robinson
Journal:  Appl Clin Genet       Date:  2015-06-16

3.  Mitral valve prolapse syndrome and MASS phenotype: Stability of aortic dilatation but progression of mitral valve prolapse.

Authors:  Moritz Rippe; Julie De Backer; Kerstin Kutsche; Laura Muiño Mosquera; Helke Schüler; Meike Rybczynski; Alexander M Bernhardt; Britta Keyser; Mathias Hillebrand; Thomas S Mir; Jürgen Berger; Stefan Blankenberg; Dietmar Koschyk; Yskert von Kodolitsch
Journal:  Int J Cardiol Heart Vasc       Date:  2016-01-21

4.  Cysteine Substitution and Calcium-Binding Mutations in FBN1 cbEGF-Like Domains Are Associated With Severe Ocular Involvement in Patients With Congenital Ectopia Lentis.

Authors:  Min Zhang; Zexu Chen; Tianhui Chen; Xiaodong Sun; Yongxiang Jiang
Journal:  Front Cell Dev Biol       Date:  2022-02-14

5.  Concomitant cardiovascular malformations in isolated bicuspid aortic valve disease: a retrospective cross-sectional study and meta-analysis.

Authors:  Katalin Szöcs; Betül Toprak; Gerhard Schön; Meike Rybczynski; Tatjana Brinken; Adrian Mahlmann; Evaldas Girdauskas; Stefan Blankenberg; Yskert von Kodolitsch
Journal:  Cardiovasc Diagn Ther       Date:  2022-08

Review 6.  Genotype-phenotype correlations of marfan syndrome and related fibrillinopathies: Phenomenon and molecular relevance.

Authors:  Ze-Xu Chen; Wan-Nan Jia; Yong-Xiang Jiang
Journal:  Front Genet       Date:  2022-08-16       Impact factor: 4.772

7.  Observational cohort study of ventricular arrhythmia in adults with Marfan syndrome caused by FBN1 mutations.

Authors:  Ali Aydin; Baran A Adsay; Sara Sheikhzadeh; Britta Keyser; Meike Rybczynski; Claudia Sondermann; Christian Detter; Daniel Steven; Peter N Robinson; Jürgen Berger; Jörg Schmidtke; Stefan Blankenberg; Stephan Willems; Yskert von Kodolitsch; Boris A Hoffmann
Journal:  PLoS One       Date:  2013-12-13       Impact factor: 3.240

8.  Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome.

Authors:  Kristina Mühlstädt; Julie De Backer; Yskert von Kodolitsch; Kerstin Kutsche; Laura Muiño Mosquera; Jens Brickwedel; Evaldas Girdauskas; Thomas S Mir; Adrian Mahlmann; Nikolaos Tsilimparis; Axel Staebler; Lauritz Schoof; Heide Seidel; Jürgen Berger; Alexander M Bernhardt; Stefan Blankenberg; Tilo Kölbel; Christian Detter; Katalin Szöcs; Harald Kaemmerer
Journal:  J Clin Med       Date:  2019-11-29       Impact factor: 4.241

  8 in total

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