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Quantification of global myocardial oxygenation in humans: initial experience

PURPOSE: To assess the feasibility of our newly developed cardiovascular magnetic resonance (CMR) methods to quantify global and/or regional myocardial oxygen consumption rate (MVO(2)) at rest and during pharmacologically-induced vasodilation in normal volunteers. METHODS: A breath-hold T(2 )quantif...

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Autores principales: McCommis, Kyle S, O'Connor, Robert, Lesniak, Donna, Lyons, Matt, Woodard, Pamela K, Gropler, Robert J, Zheng, Jie
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890683/
https://www.ncbi.nlm.nih.gov/pubmed/20525217
http://dx.doi.org/10.1186/1532-429X-12-34
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author McCommis, Kyle S
O'Connor, Robert
Lesniak, Donna
Lyons, Matt
Woodard, Pamela K
Gropler, Robert J
Zheng, Jie
author_facet McCommis, Kyle S
O'Connor, Robert
Lesniak, Donna
Lyons, Matt
Woodard, Pamela K
Gropler, Robert J
Zheng, Jie
author_sort McCommis, Kyle S
collection PubMed
description PURPOSE: To assess the feasibility of our newly developed cardiovascular magnetic resonance (CMR) methods to quantify global and/or regional myocardial oxygen consumption rate (MVO(2)) at rest and during pharmacologically-induced vasodilation in normal volunteers. METHODS: A breath-hold T(2 )quantification method is developed to calculate oxygen extraction fraction (OEF) and MVO(2 )rate at rest and/or during hyperemia, using a two-compartment model. A previously reported T(2 )quantification method using turbo-spin-echo sequence was also applied for comparison. CMR scans were performed in 6 normal volunteers. Each imaging session consisted of imaging at rest and during adenosine-induced vasodilation. The new T(2 )quantification method was applied to calculate T(2 )in the coronary sinus (CS), as well as in myocardial tissue. Resting CS OEF, representing resting global myocardial OEF, and myocardial OEF during adenosine vasodilation were then calculated by the model. Myocardial blood flow (MBF) was also obtained to calculate MVO(2), by using a first-pass perfusion imaging approach. RESULTS: The T(2 )quantification method yielded a hyperemic OEF of 0.37 ± 0.05 and a hyperemic MVO(2 )of 9.2 ± 2.4 μmol/g/min. The corresponding resting values were 0.73 ± 0.05 and 5.2 ± 1.7 μmol/g/min respectively, which agreed well with published literature values. The MVO(2 )rose proportionally with rate-pressure product from the rest condition. The T(2 )sensitivity is approximately 95% higher with the new T(2 )method than turbo-spin-echo method. CONCLUSION: The CMR oxygenation method demonstrates the potential for non-invasive estimation of myocardial oxygenation, and should be explored in patients with altered myocardial oxygenation.
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spelling pubmed-28906832010-06-24 Quantification of global myocardial oxygenation in humans: initial experience McCommis, Kyle S O'Connor, Robert Lesniak, Donna Lyons, Matt Woodard, Pamela K Gropler, Robert J Zheng, Jie J Cardiovasc Magn Reson Technical notes PURPOSE: To assess the feasibility of our newly developed cardiovascular magnetic resonance (CMR) methods to quantify global and/or regional myocardial oxygen consumption rate (MVO(2)) at rest and during pharmacologically-induced vasodilation in normal volunteers. METHODS: A breath-hold T(2 )quantification method is developed to calculate oxygen extraction fraction (OEF) and MVO(2 )rate at rest and/or during hyperemia, using a two-compartment model. A previously reported T(2 )quantification method using turbo-spin-echo sequence was also applied for comparison. CMR scans were performed in 6 normal volunteers. Each imaging session consisted of imaging at rest and during adenosine-induced vasodilation. The new T(2 )quantification method was applied to calculate T(2 )in the coronary sinus (CS), as well as in myocardial tissue. Resting CS OEF, representing resting global myocardial OEF, and myocardial OEF during adenosine vasodilation were then calculated by the model. Myocardial blood flow (MBF) was also obtained to calculate MVO(2), by using a first-pass perfusion imaging approach. RESULTS: The T(2 )quantification method yielded a hyperemic OEF of 0.37 ± 0.05 and a hyperemic MVO(2 )of 9.2 ± 2.4 μmol/g/min. The corresponding resting values were 0.73 ± 0.05 and 5.2 ± 1.7 μmol/g/min respectively, which agreed well with published literature values. The MVO(2 )rose proportionally with rate-pressure product from the rest condition. The T(2 )sensitivity is approximately 95% higher with the new T(2 )method than turbo-spin-echo method. CONCLUSION: The CMR oxygenation method demonstrates the potential for non-invasive estimation of myocardial oxygenation, and should be explored in patients with altered myocardial oxygenation. BioMed Central 2010-06-02 /pmc/articles/PMC2890683/ /pubmed/20525217 http://dx.doi.org/10.1186/1532-429X-12-34 Text en Copyright ©2010 McCommis 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 Technical notes
McCommis, Kyle S
O'Connor, Robert
Lesniak, Donna
Lyons, Matt
Woodard, Pamela K
Gropler, Robert J
Zheng, Jie
Quantification of global myocardial oxygenation in humans: initial experience
title Quantification of global myocardial oxygenation in humans: initial experience
title_full Quantification of global myocardial oxygenation in humans: initial experience
title_fullStr Quantification of global myocardial oxygenation in humans: initial experience
title_full_unstemmed Quantification of global myocardial oxygenation in humans: initial experience
title_short Quantification of global myocardial oxygenation in humans: initial experience
title_sort quantification of global myocardial oxygenation in humans: initial experience
topic Technical notes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890683/
https://www.ncbi.nlm.nih.gov/pubmed/20525217
http://dx.doi.org/10.1186/1532-429X-12-34
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