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MR Vascular Fingerprinting in Stroke and Brain Tumors Models
In this study, we evaluated an MRI fingerprinting approach (MRvF) designed to provide high-resolution parametric maps of the microvascular architecture (i.e., blood volume fraction, vessel diameter) and function (blood oxygenation) simultaneously. The method was tested in rats (n = 115), divided in...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121626/ https://www.ncbi.nlm.nih.gov/pubmed/27883015 http://dx.doi.org/10.1038/srep37071 |
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author | Lemasson, B. Pannetier, N. Coquery, N. Boisserand, Ligia S. B. Collomb, Nora Schuff, N. Moseley, M. Zaharchuk, G. Barbier, E. L. Christen, T. |
author_facet | Lemasson, B. Pannetier, N. Coquery, N. Boisserand, Ligia S. B. Collomb, Nora Schuff, N. Moseley, M. Zaharchuk, G. Barbier, E. L. Christen, T. |
author_sort | Lemasson, B. |
collection | PubMed |
description | In this study, we evaluated an MRI fingerprinting approach (MRvF) designed to provide high-resolution parametric maps of the microvascular architecture (i.e., blood volume fraction, vessel diameter) and function (blood oxygenation) simultaneously. The method was tested in rats (n = 115), divided in 3 models: brain tumors (9 L, C6, F98), permanent stroke, and a control group of healthy animals. We showed that fingerprinting can robustly distinguish between healthy and pathological brain tissues with different behaviors in tumor and stroke models. In particular, fingerprinting revealed that C6 and F98 glioma models have similar signatures while 9 L present a distinct evolution. We also showed that it is possible to improve the results of MRvF and obtain supplemental information by changing the numerical representation of the vascular network. Finally, good agreement was found between MRvF and conventional MR approaches in healthy tissues and in the C6, F98, and permanent stroke models. For the 9 L glioma model, fingerprinting showed blood oxygenation measurements that contradict results obtained with a quantitative BOLD approach. In conclusion, MR vascular fingerprinting seems to be an efficient technique to study microvascular properties in vivo. Multiple technical improvements are feasible and might improve diagnosis and management of brain diseases. |
format | Online Article Text |
id | pubmed-5121626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51216262016-11-28 MR Vascular Fingerprinting in Stroke and Brain Tumors Models Lemasson, B. Pannetier, N. Coquery, N. Boisserand, Ligia S. B. Collomb, Nora Schuff, N. Moseley, M. Zaharchuk, G. Barbier, E. L. Christen, T. Sci Rep Article In this study, we evaluated an MRI fingerprinting approach (MRvF) designed to provide high-resolution parametric maps of the microvascular architecture (i.e., blood volume fraction, vessel diameter) and function (blood oxygenation) simultaneously. The method was tested in rats (n = 115), divided in 3 models: brain tumors (9 L, C6, F98), permanent stroke, and a control group of healthy animals. We showed that fingerprinting can robustly distinguish between healthy and pathological brain tissues with different behaviors in tumor and stroke models. In particular, fingerprinting revealed that C6 and F98 glioma models have similar signatures while 9 L present a distinct evolution. We also showed that it is possible to improve the results of MRvF and obtain supplemental information by changing the numerical representation of the vascular network. Finally, good agreement was found between MRvF and conventional MR approaches in healthy tissues and in the C6, F98, and permanent stroke models. For the 9 L glioma model, fingerprinting showed blood oxygenation measurements that contradict results obtained with a quantitative BOLD approach. In conclusion, MR vascular fingerprinting seems to be an efficient technique to study microvascular properties in vivo. Multiple technical improvements are feasible and might improve diagnosis and management of brain diseases. Nature Publishing Group 2016-11-24 /pmc/articles/PMC5121626/ /pubmed/27883015 http://dx.doi.org/10.1038/srep37071 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lemasson, B. Pannetier, N. Coquery, N. Boisserand, Ligia S. B. Collomb, Nora Schuff, N. Moseley, M. Zaharchuk, G. Barbier, E. L. Christen, T. MR Vascular Fingerprinting in Stroke and Brain Tumors Models |
title | MR Vascular Fingerprinting in Stroke and Brain Tumors Models |
title_full | MR Vascular Fingerprinting in Stroke and Brain Tumors Models |
title_fullStr | MR Vascular Fingerprinting in Stroke and Brain Tumors Models |
title_full_unstemmed | MR Vascular Fingerprinting in Stroke and Brain Tumors Models |
title_short | MR Vascular Fingerprinting in Stroke and Brain Tumors Models |
title_sort | mr vascular fingerprinting in stroke and brain tumors models |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121626/ https://www.ncbi.nlm.nih.gov/pubmed/27883015 http://dx.doi.org/10.1038/srep37071 |
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