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Resting cerebral oxygen metabolism exhibits archetypal network features
Standard magnetic resonance imaging approaches offer high‐resolution but indirect measures of neural activity, limiting understanding of the physiological processes associated with imaging findings. Here, we used calibrated functional magnetic resonance imaging during the resting state to recover lo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8046048/ https://www.ncbi.nlm.nih.gov/pubmed/33544446 http://dx.doi.org/10.1002/hbm.25352 |
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author | Hubbard, Nicholas A. Turner, Monroe P. Sitek, Kevin R. West, Kathryn L. Kaczmarzyk, Jakub R. Himes, Lyndahl Thomas, Binu P. Lu, Hanzhang Rypma, Bart |
author_facet | Hubbard, Nicholas A. Turner, Monroe P. Sitek, Kevin R. West, Kathryn L. Kaczmarzyk, Jakub R. Himes, Lyndahl Thomas, Binu P. Lu, Hanzhang Rypma, Bart |
author_sort | Hubbard, Nicholas A. |
collection | PubMed |
description | Standard magnetic resonance imaging approaches offer high‐resolution but indirect measures of neural activity, limiting understanding of the physiological processes associated with imaging findings. Here, we used calibrated functional magnetic resonance imaging during the resting state to recover low‐frequency fluctuations of the cerebral metabolic rate of oxygen (CMRO(2)). We tested whether functional connections derived from these fluctuations exhibited organization properties similar to those established by previous standard functional and anatomical connectivity studies. Seventeen participants underwent 20 min of resting imaging during dual‐echo, pseudocontinuous arterial spin labeling, and blood‐oxygen‐level dependent (BOLD) signal acquisition. Participants also underwent a 10 min normocapnic and hypercapnic procedure. Brain‐wide, CMRO(2) low‐frequency fluctuations were subjected to graph‐based and voxel‐wise functional connectivity analyses. Results demonstrated that connections derived from resting CMRO(2) fluctuations exhibited complex, small‐world topological properties (i.e., high integration and segregation, cost efficiency) consistent with those observed in previous studies using functional and anatomical connectivity approaches. Voxel‐wise CMRO(2) connectivity also exhibited spatial patterns consistent with four targeted resting‐state subnetworks: two association (i.e., frontoparietal and default mode) and two perceptual (i.e., auditory and occipital‐visual). These are the first findings to support the use of calibration‐derived CMRO(2) low‐frequency fluctuations for detecting brain‐wide organizational properties typical of healthy participants. We discuss interpretations, advantages, and challenges in using calibration‐derived oxygen metabolism signals for examining the intrinsic organization of the human brain. |
format | Online Article Text |
id | pubmed-8046048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80460482021-04-16 Resting cerebral oxygen metabolism exhibits archetypal network features Hubbard, Nicholas A. Turner, Monroe P. Sitek, Kevin R. West, Kathryn L. Kaczmarzyk, Jakub R. Himes, Lyndahl Thomas, Binu P. Lu, Hanzhang Rypma, Bart Hum Brain Mapp Technical Reports Standard magnetic resonance imaging approaches offer high‐resolution but indirect measures of neural activity, limiting understanding of the physiological processes associated with imaging findings. Here, we used calibrated functional magnetic resonance imaging during the resting state to recover low‐frequency fluctuations of the cerebral metabolic rate of oxygen (CMRO(2)). We tested whether functional connections derived from these fluctuations exhibited organization properties similar to those established by previous standard functional and anatomical connectivity studies. Seventeen participants underwent 20 min of resting imaging during dual‐echo, pseudocontinuous arterial spin labeling, and blood‐oxygen‐level dependent (BOLD) signal acquisition. Participants also underwent a 10 min normocapnic and hypercapnic procedure. Brain‐wide, CMRO(2) low‐frequency fluctuations were subjected to graph‐based and voxel‐wise functional connectivity analyses. Results demonstrated that connections derived from resting CMRO(2) fluctuations exhibited complex, small‐world topological properties (i.e., high integration and segregation, cost efficiency) consistent with those observed in previous studies using functional and anatomical connectivity approaches. Voxel‐wise CMRO(2) connectivity also exhibited spatial patterns consistent with four targeted resting‐state subnetworks: two association (i.e., frontoparietal and default mode) and two perceptual (i.e., auditory and occipital‐visual). These are the first findings to support the use of calibration‐derived CMRO(2) low‐frequency fluctuations for detecting brain‐wide organizational properties typical of healthy participants. We discuss interpretations, advantages, and challenges in using calibration‐derived oxygen metabolism signals for examining the intrinsic organization of the human brain. John Wiley & Sons, Inc. 2021-02-05 /pmc/articles/PMC8046048/ /pubmed/33544446 http://dx.doi.org/10.1002/hbm.25352 Text en © 2021 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Technical Reports Hubbard, Nicholas A. Turner, Monroe P. Sitek, Kevin R. West, Kathryn L. Kaczmarzyk, Jakub R. Himes, Lyndahl Thomas, Binu P. Lu, Hanzhang Rypma, Bart Resting cerebral oxygen metabolism exhibits archetypal network features |
title | Resting cerebral oxygen metabolism exhibits archetypal network features |
title_full | Resting cerebral oxygen metabolism exhibits archetypal network features |
title_fullStr | Resting cerebral oxygen metabolism exhibits archetypal network features |
title_full_unstemmed | Resting cerebral oxygen metabolism exhibits archetypal network features |
title_short | Resting cerebral oxygen metabolism exhibits archetypal network features |
title_sort | resting cerebral oxygen metabolism exhibits archetypal network features |
topic | Technical Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8046048/ https://www.ncbi.nlm.nih.gov/pubmed/33544446 http://dx.doi.org/10.1002/hbm.25352 |
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