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The relationship between coronary artery distensibility and fractional flow reserve

Discordance between angiography-based anatomical assessment of coronary stenosis severity and fractional flow reserve (FFR) has been attributed to several factors including lesion length and irregularity, and the myocardial territory supplied by the target vessel. We sought to examine if coronary ar...

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Autores principales: Yong, Andy S. C., Javadzadegan, Ashkan, Fearon, William F., Moshfegh, Abouzar, Lau, Jerrett K., Nicholls, Stephen, Ng, Martin K. C., Kritharides, Leonard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5526528/
https://www.ncbi.nlm.nih.gov/pubmed/28742827
http://dx.doi.org/10.1371/journal.pone.0181824
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author Yong, Andy S. C.
Javadzadegan, Ashkan
Fearon, William F.
Moshfegh, Abouzar
Lau, Jerrett K.
Nicholls, Stephen
Ng, Martin K. C.
Kritharides, Leonard
author_facet Yong, Andy S. C.
Javadzadegan, Ashkan
Fearon, William F.
Moshfegh, Abouzar
Lau, Jerrett K.
Nicholls, Stephen
Ng, Martin K. C.
Kritharides, Leonard
author_sort Yong, Andy S. C.
collection PubMed
description Discordance between angiography-based anatomical assessment of coronary stenosis severity and fractional flow reserve (FFR) has been attributed to several factors including lesion length and irregularity, and the myocardial territory supplied by the target vessel. We sought to examine if coronary arterial distensibility is an independent contributor to this discordance. There were two parts to this study. The first consisted of “in silico” models of 26 human coronary arteries. Computational fluid dynamics-derived FFR was calculated for fully rigid, partially distensible and fully distensible models of the 26 arteries. The second part of the study consisted of 104 patients who underwent coronary angiography and FFR measurement. Distensibility at the lesion site (Distensibility(MLA)) and for the reference vessel (Distensibility(Ref)) was determined by analysing three-dimensional angiography images during end-systole and end-diastole. Computational fluid dynamics-derived FFR was 0.67±0.19, 0.70±0.18 and 0.75±0.17 (P<0.001) in the fully rigid, partially distensible and fully distensible models respectively. FFR correlated with both Distensibility(MLA) (r = 0.36, P<0.001) and Distensibility(Ref) (r = 0.44, P<0.001). Two-way ANCOVA analysis revealed that Distensibility(MLA) (F (1, 100) = 4.17, p = 0.031) and percentage diameter stenosis (F (1, 100) = 60.30, p < 0.01) were both independent predictors of FFR. Coronary arterial distensibility is a novel, independent determinant of FFR, and an important factor contributing to the discordance between anatomical and functional assessment of stenosis severity.
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spelling pubmed-55265282017-08-07 The relationship between coronary artery distensibility and fractional flow reserve Yong, Andy S. C. Javadzadegan, Ashkan Fearon, William F. Moshfegh, Abouzar Lau, Jerrett K. Nicholls, Stephen Ng, Martin K. C. Kritharides, Leonard PLoS One Research Article Discordance between angiography-based anatomical assessment of coronary stenosis severity and fractional flow reserve (FFR) has been attributed to several factors including lesion length and irregularity, and the myocardial territory supplied by the target vessel. We sought to examine if coronary arterial distensibility is an independent contributor to this discordance. There were two parts to this study. The first consisted of “in silico” models of 26 human coronary arteries. Computational fluid dynamics-derived FFR was calculated for fully rigid, partially distensible and fully distensible models of the 26 arteries. The second part of the study consisted of 104 patients who underwent coronary angiography and FFR measurement. Distensibility at the lesion site (Distensibility(MLA)) and for the reference vessel (Distensibility(Ref)) was determined by analysing three-dimensional angiography images during end-systole and end-diastole. Computational fluid dynamics-derived FFR was 0.67±0.19, 0.70±0.18 and 0.75±0.17 (P<0.001) in the fully rigid, partially distensible and fully distensible models respectively. FFR correlated with both Distensibility(MLA) (r = 0.36, P<0.001) and Distensibility(Ref) (r = 0.44, P<0.001). Two-way ANCOVA analysis revealed that Distensibility(MLA) (F (1, 100) = 4.17, p = 0.031) and percentage diameter stenosis (F (1, 100) = 60.30, p < 0.01) were both independent predictors of FFR. Coronary arterial distensibility is a novel, independent determinant of FFR, and an important factor contributing to the discordance between anatomical and functional assessment of stenosis severity. Public Library of Science 2017-07-25 /pmc/articles/PMC5526528/ /pubmed/28742827 http://dx.doi.org/10.1371/journal.pone.0181824 Text en © 2017 Yong et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Yong, Andy S. C.
Javadzadegan, Ashkan
Fearon, William F.
Moshfegh, Abouzar
Lau, Jerrett K.
Nicholls, Stephen
Ng, Martin K. C.
Kritharides, Leonard
The relationship between coronary artery distensibility and fractional flow reserve
title The relationship between coronary artery distensibility and fractional flow reserve
title_full The relationship between coronary artery distensibility and fractional flow reserve
title_fullStr The relationship between coronary artery distensibility and fractional flow reserve
title_full_unstemmed The relationship between coronary artery distensibility and fractional flow reserve
title_short The relationship between coronary artery distensibility and fractional flow reserve
title_sort relationship between coronary artery distensibility and fractional flow reserve
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5526528/
https://www.ncbi.nlm.nih.gov/pubmed/28742827
http://dx.doi.org/10.1371/journal.pone.0181824
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