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Exercise‐stimulated arterial transit time in calf muscles measured by dynamic contrast‐enhanced magnetic resonance imaging

The primary goal of this study was to evaluate arterial transit time (ATT) in exercise‐stimulated calf muscles as a promising indicator of muscle function. Following plantar flexion, ATT was measured by dynamic contrast‐enhanced (DCE) MRI in young and elderly healthy subjects and patients with perip...

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Autores principales: Conlin, Christopher C., Layec, Gwenael, Hanrahan, Christopher J., Hu, Nan, Mueller, Michelle T., Lee, Vivian S., Zhang, Jeff L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333626/
https://www.ncbi.nlm.nih.gov/pubmed/30648355
http://dx.doi.org/10.14814/phy2.13978
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author Conlin, Christopher C.
Layec, Gwenael
Hanrahan, Christopher J.
Hu, Nan
Mueller, Michelle T.
Lee, Vivian S.
Zhang, Jeff L.
author_facet Conlin, Christopher C.
Layec, Gwenael
Hanrahan, Christopher J.
Hu, Nan
Mueller, Michelle T.
Lee, Vivian S.
Zhang, Jeff L.
author_sort Conlin, Christopher C.
collection PubMed
description The primary goal of this study was to evaluate arterial transit time (ATT) in exercise‐stimulated calf muscles as a promising indicator of muscle function. Following plantar flexion, ATT was measured by dynamic contrast‐enhanced (DCE) MRI in young and elderly healthy subjects and patients with peripheral artery disease (PAD). In the young healthy subjects, gastrocnemius ATT decreased significantly (P < 0.01) from 4.3 ± 1.5 to 2.4 ± 0.4 sec when exercise load increased from 4 lbs to 16 lbs. For the same load of 4 lbs, gastrocnemius ATT was lower in the elderly healthy subjects (3.2 ± 1.1 sec; P = 0.08) and in the PAD patients (2.4 ± 1.2 sec; P = 0.02) than in the young healthy subjects. While the sensitivity of the exercise‐stimulated ATT is diagnostically useful, it poses a challenge for arterial spin labeling (ASL), a noncontrast MRI method for measuring muscle perfusion. As a secondary goal of this study, we assessed the impact of ATT on ASL‐measured perfusion with ASL data of multiple post labeling delays (PLDs) acquired from a healthy subject. Perfusion varied substantially with PLD in the activated gastrocnemius, which can be attributed to the ATT variability as verified by a simulation. In conclusion, muscle ATT is sensitive to exercise intensity, and it potentially reflects the functional impact of aging and PAD on calf muscles. For precise measurement of exercise‐stimulated muscle perfusion, it is recommended that ATT be considered when quantifying muscle ASL data.
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spelling pubmed-63336262019-01-23 Exercise‐stimulated arterial transit time in calf muscles measured by dynamic contrast‐enhanced magnetic resonance imaging Conlin, Christopher C. Layec, Gwenael Hanrahan, Christopher J. Hu, Nan Mueller, Michelle T. Lee, Vivian S. Zhang, Jeff L. Physiol Rep Original Research The primary goal of this study was to evaluate arterial transit time (ATT) in exercise‐stimulated calf muscles as a promising indicator of muscle function. Following plantar flexion, ATT was measured by dynamic contrast‐enhanced (DCE) MRI in young and elderly healthy subjects and patients with peripheral artery disease (PAD). In the young healthy subjects, gastrocnemius ATT decreased significantly (P < 0.01) from 4.3 ± 1.5 to 2.4 ± 0.4 sec when exercise load increased from 4 lbs to 16 lbs. For the same load of 4 lbs, gastrocnemius ATT was lower in the elderly healthy subjects (3.2 ± 1.1 sec; P = 0.08) and in the PAD patients (2.4 ± 1.2 sec; P = 0.02) than in the young healthy subjects. While the sensitivity of the exercise‐stimulated ATT is diagnostically useful, it poses a challenge for arterial spin labeling (ASL), a noncontrast MRI method for measuring muscle perfusion. As a secondary goal of this study, we assessed the impact of ATT on ASL‐measured perfusion with ASL data of multiple post labeling delays (PLDs) acquired from a healthy subject. Perfusion varied substantially with PLD in the activated gastrocnemius, which can be attributed to the ATT variability as verified by a simulation. In conclusion, muscle ATT is sensitive to exercise intensity, and it potentially reflects the functional impact of aging and PAD on calf muscles. For precise measurement of exercise‐stimulated muscle perfusion, it is recommended that ATT be considered when quantifying muscle ASL data. John Wiley and Sons Inc. 2019-01-15 /pmc/articles/PMC6333626/ /pubmed/30648355 http://dx.doi.org/10.14814/phy2.13978 Text en © 2019 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Conlin, Christopher C.
Layec, Gwenael
Hanrahan, Christopher J.
Hu, Nan
Mueller, Michelle T.
Lee, Vivian S.
Zhang, Jeff L.
Exercise‐stimulated arterial transit time in calf muscles measured by dynamic contrast‐enhanced magnetic resonance imaging
title Exercise‐stimulated arterial transit time in calf muscles measured by dynamic contrast‐enhanced magnetic resonance imaging
title_full Exercise‐stimulated arterial transit time in calf muscles measured by dynamic contrast‐enhanced magnetic resonance imaging
title_fullStr Exercise‐stimulated arterial transit time in calf muscles measured by dynamic contrast‐enhanced magnetic resonance imaging
title_full_unstemmed Exercise‐stimulated arterial transit time in calf muscles measured by dynamic contrast‐enhanced magnetic resonance imaging
title_short Exercise‐stimulated arterial transit time in calf muscles measured by dynamic contrast‐enhanced magnetic resonance imaging
title_sort exercise‐stimulated arterial transit time in calf muscles measured by dynamic contrast‐enhanced magnetic resonance imaging
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333626/
https://www.ncbi.nlm.nih.gov/pubmed/30648355
http://dx.doi.org/10.14814/phy2.13978
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