Literature DB >> 25001203

Fluid dynamics of aortic root dilation in Marfan syndrome.

Giorgio Querzoli1, Stefania Fortini2, Stefania Espa2, Martina Costantini2, Francesca Sorgini2.   

Abstract

Aortic root dilation and propensity to dissection are typical manifestations of the Marfan Syndrome (MS), a genetic defect leading to the degeneration of the elastic fibres. Dilation affects the structure of the flow and, in turn, altered flow may play a role in vessel dilation, generation of aneurysms, and dissection. The aim of the present work is the investigation in-vitro of the fluid dynamic modifications occurring as a consequence of the morphological changes typically induced in the aortic root by MS. A mock-loop reproducing the left ventricle outflow tract and the aortic root was used to measure time resolved velocity maps on a longitudinal symmetry plane of the aortic root. Two dilated model aortas, designed to resemble morphological characteristics typically observed in MS patients, have been compared to a reference, healthy geometry. The aortic model was designed to quantitatively reproduce the change of aortic distensibility caused by MS. Results demonstrate that vorticity released from the valve leaflets, and possibly accumulating in the root, plays a fundamental role in redirecting the systolic jet issued from the aortic valve. The altered systolic flow also determines a different residual flow during the diastole.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Aortic flow; Fluid dynamics; Marfan syndrome; Velocity mapping; Vortex dynamics

Mesh:

Year:  2014        PMID: 25001203     DOI: 10.1016/j.jbiomech.2014.06.025

Source DB:  PubMed          Journal:  J Biomech        ISSN: 0021-9290            Impact factor:   2.712


  4 in total

1.  Aortic root anatomy as a factor in the fluid mechanics of transcatheter aortic valve replacement.

Authors:  Muralidhar Padala
Journal:  J Thorac Cardiovasc Surg       Date:  2018-10-28       Impact factor: 5.209

2.  Integrated strategy for in vitro characterization of a bileaflet mechanical aortic valve.

Authors:  Francesca Maria Susin; Stefania Espa; Riccardo Toninato; Stefania Fortini; Giorgio Querzoli
Journal:  Biomed Eng Online       Date:  2017-02-16       Impact factor: 2.819

3.  Altered aortic 3D hemodynamics and geometry in pediatric Marfan syndrome patients.

Authors:  Roel L F van der Palen; Alex J Barker; Emilie Bollache; Julio Garcia; Michael J Rose; Pim van Ooij; Luciana T Young; Arno A W Roest; Michael Markl; Joshua D Robinson; Cynthia K Rigsby
Journal:  J Cardiovasc Magn Reson       Date:  2017-03-17       Impact factor: 5.364

4.  Association of thoracic spine deformity and cardiovascular disease in a mouse model for Marfan syndrome.

Authors:  Rodrigo Barbosa de Souza; Luis Ernesto Farinha-Arcieri; Marcia Helena Braga Catroxo; Ana Maria Cristina Rebelo Pinto da Fonseca Martins; Roberto Carlos Tedesco; Luis Garcia Alonso; Ivan Hong Jun Koh; Lygia V Pereira
Journal:  PLoS One       Date:  2019-11-14       Impact factor: 3.240

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.