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Mapping of whole‐cerebrum resting‐state networks using ultra‐high resolution acquisition protocols
Resting‐state functional magnetic resonance imaging (fMRI) has been used in numerous studies to map networks in the brain that employ spatially disparate regions. However, attempts to map networks with high spatial resolution have been hampered by conflicting technical demands and associated problem...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248311/ https://www.ncbi.nlm.nih.gov/pubmed/35384130 http://dx.doi.org/10.1002/hbm.25855 |
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author | Yun, Seong Dae Pais‐Roldán, Patricia Palomero‐Gallagher, Nicola Shah, N. Jon |
author_facet | Yun, Seong Dae Pais‐Roldán, Patricia Palomero‐Gallagher, Nicola Shah, N. Jon |
author_sort | Yun, Seong Dae |
collection | PubMed |
description | Resting‐state functional magnetic resonance imaging (fMRI) has been used in numerous studies to map networks in the brain that employ spatially disparate regions. However, attempts to map networks with high spatial resolution have been hampered by conflicting technical demands and associated problems. Results from recent fMRI studies have shown that spatial resolution remains around 0.7 × 0.7 × 0.7 mm(3), with only partial brain coverage. Therefore, this work aims to present a novel fMRI technique that was developed based on echo‐planar‐imaging with keyhole (EPIK) combined with repetition‐time‐external (TR‐external) EPI phase correction. Each technique has been previously shown to be effective in enhancing the spatial resolution of fMRI, and in this work, the combination of the two techniques into TR‐external EPIK provided a nominal spatial resolution of 0.51 × 0.51 × 1.00 mm(3) (0.26 mm(3) voxel) with whole‐cerebrum coverage. Here, the feasibility of using half‐millimetre in‐plane TR‐external EPIK for resting‐state fMRI was validated using 13 healthy subjects and the corresponding reproducible mapping of resting‐state networks was demonstrated. Furthermore, TR‐external EPIK enabled the identification of various resting‐state networks distributed throughout the brain from a single fMRI session, with mapping fidelity onto the grey matter at 7T. The high‐resolution functional image further revealed mesoscale anatomical structures, such as small cerebral vessels and the internal granular layer of the cortex within the postcentral gyrus. |
format | Online Article Text |
id | pubmed-9248311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92483112022-07-05 Mapping of whole‐cerebrum resting‐state networks using ultra‐high resolution acquisition protocols Yun, Seong Dae Pais‐Roldán, Patricia Palomero‐Gallagher, Nicola Shah, N. Jon Hum Brain Mapp Research Articles Resting‐state functional magnetic resonance imaging (fMRI) has been used in numerous studies to map networks in the brain that employ spatially disparate regions. However, attempts to map networks with high spatial resolution have been hampered by conflicting technical demands and associated problems. Results from recent fMRI studies have shown that spatial resolution remains around 0.7 × 0.7 × 0.7 mm(3), with only partial brain coverage. Therefore, this work aims to present a novel fMRI technique that was developed based on echo‐planar‐imaging with keyhole (EPIK) combined with repetition‐time‐external (TR‐external) EPI phase correction. Each technique has been previously shown to be effective in enhancing the spatial resolution of fMRI, and in this work, the combination of the two techniques into TR‐external EPIK provided a nominal spatial resolution of 0.51 × 0.51 × 1.00 mm(3) (0.26 mm(3) voxel) with whole‐cerebrum coverage. Here, the feasibility of using half‐millimetre in‐plane TR‐external EPIK for resting‐state fMRI was validated using 13 healthy subjects and the corresponding reproducible mapping of resting‐state networks was demonstrated. Furthermore, TR‐external EPIK enabled the identification of various resting‐state networks distributed throughout the brain from a single fMRI session, with mapping fidelity onto the grey matter at 7T. The high‐resolution functional image further revealed mesoscale anatomical structures, such as small cerebral vessels and the internal granular layer of the cortex within the postcentral gyrus. John Wiley & Sons, Inc. 2022-04-06 /pmc/articles/PMC9248311/ /pubmed/35384130 http://dx.doi.org/10.1002/hbm.25855 Text en © 2022 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Yun, Seong Dae Pais‐Roldán, Patricia Palomero‐Gallagher, Nicola Shah, N. Jon Mapping of whole‐cerebrum resting‐state networks using ultra‐high resolution acquisition protocols |
title | Mapping of whole‐cerebrum resting‐state networks using ultra‐high resolution acquisition protocols |
title_full | Mapping of whole‐cerebrum resting‐state networks using ultra‐high resolution acquisition protocols |
title_fullStr | Mapping of whole‐cerebrum resting‐state networks using ultra‐high resolution acquisition protocols |
title_full_unstemmed | Mapping of whole‐cerebrum resting‐state networks using ultra‐high resolution acquisition protocols |
title_short | Mapping of whole‐cerebrum resting‐state networks using ultra‐high resolution acquisition protocols |
title_sort | mapping of whole‐cerebrum resting‐state networks using ultra‐high resolution acquisition protocols |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248311/ https://www.ncbi.nlm.nih.gov/pubmed/35384130 http://dx.doi.org/10.1002/hbm.25855 |
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