Literature DB >> 33280029

Mitral annulus disjunction is associated with adverse outcome in Marfan and Loeys-Dietz syndromes.

Monica Chivulescu1,2, Kirsten Krohg-Sørensen2,3, Esther Scheirlynck1, Beate R Lindberg3, Lars A Dejgaard1,2,4, Øyvind H Lie1,2, Thomas Helle-Valle1, Eystein T Skjølsvik1,2, Mette E Estensen1, Thor Edvardsen1,2,4, Per S Lingaas3, Kristina H Haugaa1,2.   

Abstract

AIMS: We aimed to assess the prevalence of mitral annulus disjunction (MAD) and to explore the association with aortic disease and mitral valve surgery in patients with Marfan syndrome (MFS) and Loeys-Dietz syndrome (LDS). METHODS AND
RESULTS: We included consecutive MFS patients fulfilling Revised Ghent Criteria and LDS patients fulfilling Loeys-Dietz Revised Nosology. MAD was identified by echocardiography and was quantified as the longitudinal distance from the ventricular myocardium to the hinge point of the posterior mitral leaflet. Aortic events were defined as aortic dissection or prophylactic aortic surgery. We recorded the need of mitral valve surgery including mitral valve repair or replacement. We included 168 patients (103 with MFS and 65 with LDS). The prevalence of MAD was 41%. MAD was present in all age groups. Aortic events occurred in 112 (67%) patients (27 with dissections and 85 with prophylactic surgical interventions). Patients with MAD were younger at aortic event than those without MAD (log rank = 0.02) Patients with aortic events had greater MAD distance in posterolateral wall [8 (7-10) mm vs. 7 (6-8) mm, P = 0.04]. Mitral events occurred more frequently in patients with MAD (P < 0.001).
CONCLUSION: MAD was highly prevalent in patients with MFS and LDS. MAD was a marker of severe disease including aortic events at younger age and need of mitral valve surgery. Screening patients with MFS an LDS for MAD may provide prognostic information and may be relevant in planning surgical intervention. Detection of MAD in patients with MFS and LDS may infer closer clinical follow-up from younger age.
© The Author(s) 2020. Published by Oxford University Press on behalf of the European Society of Cardiology.

Entities:  

Keywords:  Loeys–Dietz; Marfan; aortic syndrome; mitral annulus disjunction; mitral valve disease; mitral valve prolapse

Year:  2020        PMID: 33280029     DOI: 10.1093/ehjci/jeaa324

Source DB:  PubMed          Journal:  Eur Heart J Cardiovasc Imaging        ISSN: 2047-2404            Impact factor:   6.875


  5 in total

Review 1.  Marfan syndrome.

Authors:  Dianna M Milewicz; Alan C Braverman; Julie De Backer; Shaine A Morris; Catherine Boileau; Irene H Maumenee; Guillaume Jondeau; Arturo Evangelista; Reed E Pyeritz
Journal:  Nat Rev Dis Primers       Date:  2021-09-02       Impact factor: 65.038

2.  Mitral annular disjunction in patients with severe aortic stenosis: Extent and reproducibility of measurements with computed tomography.

Authors:  T Tsianaka; I Matziris; A Kobe; A Euler; N Kuzo; L Erhart; S Leschka; R Manka; A M Kasel; F C Tanner; H Alkadhi; M Eberhard
Journal:  Eur J Radiol Open       Date:  2021-03-09

3.  Arrhythmic Mitral Valve Prolapse and Mitral Annulus Disjunction in Heritable Aortic Disease.

Authors:  Drake A Comber; Ashley DeGraaf; Derek Human; Amanda Barlow; Praveen Indraratna; Gnalini Sathananthan; Zachary Laksman
Journal:  CJC Open       Date:  2021-07-01

4.  Association of Mitral Annular Disjunction With Cardiovascular Outcomes Among Patients With Marfan Syndrome.

Authors:  Anthony Demolder; Frank Timmermans; Mattias Duytschaever; Laura Muiño-Mosquera; Julie De Backer
Journal:  JAMA Cardiol       Date:  2021-10-01       Impact factor: 30.154

5.  Does Anatomic Phenotype of Mitral Annular Disjunction Impact Survival? An Autopsy-Based Retrospective Study.

Authors:  Nan Zhou; Qianhao Zhao; Rui Li; Da Zheng; Yuxi Xiao; Danmi Mao; Yunyi Wang; Jiacheng Yue; Kai Zhang; Jonathan C Makielski; Jianding Cheng
Journal:  J Cardiovasc Dev Dis       Date:  2021-12-05
  5 in total

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