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Hepatic arterial spin labelling MRI: an initial evaluation in mice

The development of strategies to combat hepatic disease and augment tissue regeneration has created a need for methods to assess regional liver function. Liver perfusion imaging has the potential to fulfil this need, across a range of hepatic diseases, alongside the assessment of therapeutic respons...

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Autores principales: Ramasawmy, R, Campbell-Washburn, A E, Wells, J A, Johnson, S P, Pedley, R B, Walker-Samuel, S, Lythgoe, M F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670473/
https://www.ncbi.nlm.nih.gov/pubmed/25522098
http://dx.doi.org/10.1002/nbm.3251
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author Ramasawmy, R
Campbell-Washburn, A E
Wells, J A
Johnson, S P
Pedley, R B
Walker-Samuel, S
Lythgoe, M F
author_facet Ramasawmy, R
Campbell-Washburn, A E
Wells, J A
Johnson, S P
Pedley, R B
Walker-Samuel, S
Lythgoe, M F
author_sort Ramasawmy, R
collection PubMed
description The development of strategies to combat hepatic disease and augment tissue regeneration has created a need for methods to assess regional liver function. Liver perfusion imaging has the potential to fulfil this need, across a range of hepatic diseases, alongside the assessment of therapeutic response. In this study, the feasibility of hepatic arterial spin labelling (HASL) was assessed for the first time in mice at 9.4 T, its variability and repeatability were evaluated, and it was applied to a model of colorectal liver metastasis. Data were acquired using flow-sensitive alternating inversion recovery-arterial spin labelling (FAIR-ASL) with a Look–Locker readout, and analysed using retrospective respiratory gating and a T(1)-based quantification. This study shows that preclinical HASL is feasible and exhibits good repeatability and reproducibility. Mean estimated liver perfusion was 2.2 ± 0.8 mL/g/min (mean ± standard error, n = 10), which agrees well with previous measurements using invasive approaches. Estimates of the variation gave a within-session coefficient of variation (CV(WS)) of 7%, a between-session coefficient of variation (CV(BS)) of 9% and a between-animal coefficient of variation (CV(A)) of 15%. The within-session Bland–Altman repeatability coefficient (RC(WS)) was 18% and the between-session repeatability coefficient (RC(BS)) was 29%. Finally, the HASL method was applied to a mouse model of liver metastasis, in which significantly lower mean perfusion (1.1 ± 0.5 mL/g/min, n = 6) was measured within the tumours, as seen by fluorescence histology. These data indicate that precise and accurate liver perfusion estimates can be achieved using ASL techniques, and provide a platform for future studies investigating hepatic perfusion in mouse models of disease. Copyright © 2014 John Wiley & Sons, Ltd.
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spelling pubmed-46704732015-12-11 Hepatic arterial spin labelling MRI: an initial evaluation in mice Ramasawmy, R Campbell-Washburn, A E Wells, J A Johnson, S P Pedley, R B Walker-Samuel, S Lythgoe, M F NMR Biomed Research Articles The development of strategies to combat hepatic disease and augment tissue regeneration has created a need for methods to assess regional liver function. Liver perfusion imaging has the potential to fulfil this need, across a range of hepatic diseases, alongside the assessment of therapeutic response. In this study, the feasibility of hepatic arterial spin labelling (HASL) was assessed for the first time in mice at 9.4 T, its variability and repeatability were evaluated, and it was applied to a model of colorectal liver metastasis. Data were acquired using flow-sensitive alternating inversion recovery-arterial spin labelling (FAIR-ASL) with a Look–Locker readout, and analysed using retrospective respiratory gating and a T(1)-based quantification. This study shows that preclinical HASL is feasible and exhibits good repeatability and reproducibility. Mean estimated liver perfusion was 2.2 ± 0.8 mL/g/min (mean ± standard error, n = 10), which agrees well with previous measurements using invasive approaches. Estimates of the variation gave a within-session coefficient of variation (CV(WS)) of 7%, a between-session coefficient of variation (CV(BS)) of 9% and a between-animal coefficient of variation (CV(A)) of 15%. The within-session Bland–Altman repeatability coefficient (RC(WS)) was 18% and the between-session repeatability coefficient (RC(BS)) was 29%. Finally, the HASL method was applied to a mouse model of liver metastasis, in which significantly lower mean perfusion (1.1 ± 0.5 mL/g/min, n = 6) was measured within the tumours, as seen by fluorescence histology. These data indicate that precise and accurate liver perfusion estimates can be achieved using ASL techniques, and provide a platform for future studies investigating hepatic perfusion in mouse models of disease. Copyright © 2014 John Wiley & Sons, Ltd. Blackwell Publishing Ltd 2015-02 2014-12-17 /pmc/articles/PMC4670473/ /pubmed/25522098 http://dx.doi.org/10.1002/nbm.3251 Text en © 2014 The Authors. NMR in Biomedicine published by John Wiley & Sons, Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Ramasawmy, R
Campbell-Washburn, A E
Wells, J A
Johnson, S P
Pedley, R B
Walker-Samuel, S
Lythgoe, M F
Hepatic arterial spin labelling MRI: an initial evaluation in mice
title Hepatic arterial spin labelling MRI: an initial evaluation in mice
title_full Hepatic arterial spin labelling MRI: an initial evaluation in mice
title_fullStr Hepatic arterial spin labelling MRI: an initial evaluation in mice
title_full_unstemmed Hepatic arterial spin labelling MRI: an initial evaluation in mice
title_short Hepatic arterial spin labelling MRI: an initial evaluation in mice
title_sort hepatic arterial spin labelling mri: an initial evaluation in mice
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670473/
https://www.ncbi.nlm.nih.gov/pubmed/25522098
http://dx.doi.org/10.1002/nbm.3251
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