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Resting myocardial perfusion quantification with CMR arterial spin labeling at 1.5 T and 3.0 T

BACKGROUND: The magnetic resonance technique of arterial spin labeling (ASL) allows myocardial perfusion to be quantified without the use of a contrast agent. This study aimed to use a modified ASL technique and T(1 )regression algorithm, previously validated in canine models, to calculate myocardia...

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Autores principales: Northrup, Benjamin E, McCommis, Kyle S, Zhang, Haosen, Ray, Shuddhadeb, Woodard, Pamela K, Gropler, Robert J, Zheng, Jie
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654036/
https://www.ncbi.nlm.nih.gov/pubmed/19014709
http://dx.doi.org/10.1186/1532-429X-10-53
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author Northrup, Benjamin E
McCommis, Kyle S
Zhang, Haosen
Ray, Shuddhadeb
Woodard, Pamela K
Gropler, Robert J
Zheng, Jie
author_facet Northrup, Benjamin E
McCommis, Kyle S
Zhang, Haosen
Ray, Shuddhadeb
Woodard, Pamela K
Gropler, Robert J
Zheng, Jie
author_sort Northrup, Benjamin E
collection PubMed
description BACKGROUND: The magnetic resonance technique of arterial spin labeling (ASL) allows myocardial perfusion to be quantified without the use of a contrast agent. This study aimed to use a modified ASL technique and T(1 )regression algorithm, previously validated in canine models, to calculate myocardial blood flow (MBF) in normal human subjects and to compare the accuracy and repeatability of this calculation at 1.5 T and 3.0 T. A computer simulation was performed and compared with experimental findings. RESULTS: Eight subjects were imaged, with scans at 3.0 T showing significantly higher T(1 )values (P < 0.001) and signal-to-noise ratios (SNR) (P < 0.002) than scans at 1.5 T. The average MBF was found to be 0.990 ± 0.302 mL/g/min at 1.5 T and 1.058 ± 0.187 mL/g/min at 3.0 T. The repeatability at 3.0 T was improved 43% over that at 1.5 T, although no statistically significant difference was found between the two field strengths. In the simulation, the accuracy and the repeatability of the MBF calculations were 61% and 38% higher, respectively, at 3.0 T than at 1.5 T, but no statistically significant differences were observed. There were no significant differences between the myocardial perfusion data sets obtained from the two independent observers. Additionally, there was a trend toward less variation in the perfusion data from the two observers at 3.0 T as compared to 1.5 T. CONCLUSION: This suggests that this ASL technique can be used, preferably at 3.0 T, to quantify myocardial perfusion in humans and with further development could be useful in the clinical setting as an alternative method of perfusion analysis.
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spelling pubmed-26540362009-03-11 Resting myocardial perfusion quantification with CMR arterial spin labeling at 1.5 T and 3.0 T Northrup, Benjamin E McCommis, Kyle S Zhang, Haosen Ray, Shuddhadeb Woodard, Pamela K Gropler, Robert J Zheng, Jie J Cardiovasc Magn Reson Research BACKGROUND: The magnetic resonance technique of arterial spin labeling (ASL) allows myocardial perfusion to be quantified without the use of a contrast agent. This study aimed to use a modified ASL technique and T(1 )regression algorithm, previously validated in canine models, to calculate myocardial blood flow (MBF) in normal human subjects and to compare the accuracy and repeatability of this calculation at 1.5 T and 3.0 T. A computer simulation was performed and compared with experimental findings. RESULTS: Eight subjects were imaged, with scans at 3.0 T showing significantly higher T(1 )values (P < 0.001) and signal-to-noise ratios (SNR) (P < 0.002) than scans at 1.5 T. The average MBF was found to be 0.990 ± 0.302 mL/g/min at 1.5 T and 1.058 ± 0.187 mL/g/min at 3.0 T. The repeatability at 3.0 T was improved 43% over that at 1.5 T, although no statistically significant difference was found between the two field strengths. In the simulation, the accuracy and the repeatability of the MBF calculations were 61% and 38% higher, respectively, at 3.0 T than at 1.5 T, but no statistically significant differences were observed. There were no significant differences between the myocardial perfusion data sets obtained from the two independent observers. Additionally, there was a trend toward less variation in the perfusion data from the two observers at 3.0 T as compared to 1.5 T. CONCLUSION: This suggests that this ASL technique can be used, preferably at 3.0 T, to quantify myocardial perfusion in humans and with further development could be useful in the clinical setting as an alternative method of perfusion analysis. BioMed Central 2008-11-17 /pmc/articles/PMC2654036/ /pubmed/19014709 http://dx.doi.org/10.1186/1532-429X-10-53 Text en Copyright © 2008 Northrup 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
Northrup, Benjamin E
McCommis, Kyle S
Zhang, Haosen
Ray, Shuddhadeb
Woodard, Pamela K
Gropler, Robert J
Zheng, Jie
Resting myocardial perfusion quantification with CMR arterial spin labeling at 1.5 T and 3.0 T
title Resting myocardial perfusion quantification with CMR arterial spin labeling at 1.5 T and 3.0 T
title_full Resting myocardial perfusion quantification with CMR arterial spin labeling at 1.5 T and 3.0 T
title_fullStr Resting myocardial perfusion quantification with CMR arterial spin labeling at 1.5 T and 3.0 T
title_full_unstemmed Resting myocardial perfusion quantification with CMR arterial spin labeling at 1.5 T and 3.0 T
title_short Resting myocardial perfusion quantification with CMR arterial spin labeling at 1.5 T and 3.0 T
title_sort resting myocardial perfusion quantification with cmr arterial spin labeling at 1.5 t and 3.0 t
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654036/
https://www.ncbi.nlm.nih.gov/pubmed/19014709
http://dx.doi.org/10.1186/1532-429X-10-53
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