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First-pass perfusion CMR two days after infarction predicts severity of functional impairment six weeks later in the rat heart

BACKGROUND: In humans, dynamic contrast CMR of the first pass of a bolus infusion of Gadolinium-based contrast agent has become a standard technique to identify under-perfused regions of the heart and can accurately demonstrate the severity of myocardial infarction. Despite the clinical importance o...

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Autores principales: Stuckey, Daniel J, Carr, Carolyn A, Meader, Stephanie J, Tyler, Damian J, Cole, Mark A, Clarke, Kieran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162911/
https://www.ncbi.nlm.nih.gov/pubmed/21812990
http://dx.doi.org/10.1186/1532-429X-13-38
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author Stuckey, Daniel J
Carr, Carolyn A
Meader, Stephanie J
Tyler, Damian J
Cole, Mark A
Clarke, Kieran
author_facet Stuckey, Daniel J
Carr, Carolyn A
Meader, Stephanie J
Tyler, Damian J
Cole, Mark A
Clarke, Kieran
author_sort Stuckey, Daniel J
collection PubMed
description BACKGROUND: In humans, dynamic contrast CMR of the first pass of a bolus infusion of Gadolinium-based contrast agent has become a standard technique to identify under-perfused regions of the heart and can accurately demonstrate the severity of myocardial infarction. Despite the clinical importance of this method, it has rarely been applied in small animal models of cardiac disease. In order to identify perfusion delays in the infarcted rat heart, here we present a method in which a T(1 )weighted MR image has been acquired during each cardiac cycle. METHODS AND RESULTS: In isolated perfused rat hearts, contrast agent infusion gave uniform signal enhancement throughout the myocardium. Occlusion of the left anterior descending coronary artery significantly reduced the rate of signal enhancement in anterior regions of the heart, demonstrating that the first-pass method was sensitive to perfusion deficits. In vivo measurements of myocardial morphology, function, perfusion and viability were made at 2 and 8 days after infarction. Morphology and function were further assessed using cine-MRI at 42 days. The perfusion delay was larger in rat hearts that went on to develop greater functional impairment, demonstrating that first-pass CMR can be used as an early indicator of infarct severity. First-pass CMR at 2 and 8 days following infarction better predicted outcome than cardiac ejection fraction, end diastolic volume or end systolic volume. CONCLUSION: First-pass CMR provides a predictive measure of the severity of myocardial impairment caused by infarction in a rodent model of heart failure.
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spelling pubmed-31629112011-08-28 First-pass perfusion CMR two days after infarction predicts severity of functional impairment six weeks later in the rat heart Stuckey, Daniel J Carr, Carolyn A Meader, Stephanie J Tyler, Damian J Cole, Mark A Clarke, Kieran J Cardiovasc Magn Reson Research BACKGROUND: In humans, dynamic contrast CMR of the first pass of a bolus infusion of Gadolinium-based contrast agent has become a standard technique to identify under-perfused regions of the heart and can accurately demonstrate the severity of myocardial infarction. Despite the clinical importance of this method, it has rarely been applied in small animal models of cardiac disease. In order to identify perfusion delays in the infarcted rat heart, here we present a method in which a T(1 )weighted MR image has been acquired during each cardiac cycle. METHODS AND RESULTS: In isolated perfused rat hearts, contrast agent infusion gave uniform signal enhancement throughout the myocardium. Occlusion of the left anterior descending coronary artery significantly reduced the rate of signal enhancement in anterior regions of the heart, demonstrating that the first-pass method was sensitive to perfusion deficits. In vivo measurements of myocardial morphology, function, perfusion and viability were made at 2 and 8 days after infarction. Morphology and function were further assessed using cine-MRI at 42 days. The perfusion delay was larger in rat hearts that went on to develop greater functional impairment, demonstrating that first-pass CMR can be used as an early indicator of infarct severity. First-pass CMR at 2 and 8 days following infarction better predicted outcome than cardiac ejection fraction, end diastolic volume or end systolic volume. CONCLUSION: First-pass CMR provides a predictive measure of the severity of myocardial impairment caused by infarction in a rodent model of heart failure. BioMed Central 2011-08-03 /pmc/articles/PMC3162911/ /pubmed/21812990 http://dx.doi.org/10.1186/1532-429X-13-38 Text en Copyright ©2011 Stuckey et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Stuckey, Daniel J
Carr, Carolyn A
Meader, Stephanie J
Tyler, Damian J
Cole, Mark A
Clarke, Kieran
First-pass perfusion CMR two days after infarction predicts severity of functional impairment six weeks later in the rat heart
title First-pass perfusion CMR two days after infarction predicts severity of functional impairment six weeks later in the rat heart
title_full First-pass perfusion CMR two days after infarction predicts severity of functional impairment six weeks later in the rat heart
title_fullStr First-pass perfusion CMR two days after infarction predicts severity of functional impairment six weeks later in the rat heart
title_full_unstemmed First-pass perfusion CMR two days after infarction predicts severity of functional impairment six weeks later in the rat heart
title_short First-pass perfusion CMR two days after infarction predicts severity of functional impairment six weeks later in the rat heart
title_sort first-pass perfusion cmr two days after infarction predicts severity of functional impairment six weeks later in the rat heart
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162911/
https://www.ncbi.nlm.nih.gov/pubmed/21812990
http://dx.doi.org/10.1186/1532-429X-13-38
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