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Mapping Long-Term Functional Changes in Cerebral Blood Flow by Arterial Spin Labeling
Although arterial spin labeling (ASL) is appealing for mapping long-term changes in functional activity, inter-sessional variations in basal blood flow, arterial transit times (ATTs), and alignment errors, can result in significant false activation when comparing images from separate sessions. By ta...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5051683/ https://www.ncbi.nlm.nih.gov/pubmed/27706218 http://dx.doi.org/10.1371/journal.pone.0164112 |
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author | Ssali, Tracy Anazodo, Udunna C. Bureau, Yves MacIntosh, Bradley J. Günther, Matthias St. Lawrence, Keith |
author_facet | Ssali, Tracy Anazodo, Udunna C. Bureau, Yves MacIntosh, Bradley J. Günther, Matthias St. Lawrence, Keith |
author_sort | Ssali, Tracy |
collection | PubMed |
description | Although arterial spin labeling (ASL) is appealing for mapping long-term changes in functional activity, inter-sessional variations in basal blood flow, arterial transit times (ATTs), and alignment errors, can result in significant false activation when comparing images from separate sessions. By taking steps to reduce these sources of noise, this study assessed the ability of ASL to detect functional CBF changes between sessions. ASL data were collected in three sessions to image ATT, resting CBF and CBF changes associated with motor activation (7 participants). Activation maps were generated using rest and task images acquired in the same session and from sessions separated by up to a month. Good agreement was found when comparing between-session activation maps to within-session activation maps with only a 16% decrease in precision (within-session: 90 ± 7%) and a 13% decrease in the Dice similarity (within-session: 0.75 ± 0.07) coefficient after a month. In addition, voxel-wise reproducibility (within-session: 4.7 ± 4.5%) and reliability (within-session: 0.89 ± 0.20) of resting grey-matter CBF decreased by less than 18% for the between-session analysis relative to within-session values. ATT variability between sessions (5.0 ± 2.7%) was roughly half the between-subject variability, indicating that its effects on longitudinal CBF were minimal. These results demonstrate that conducting voxel-wise analysis on CBF images acquired on different days is feasible with only modest loss in precision, highlighting the potential of ASL for longitudinal studies. |
format | Online Article Text |
id | pubmed-5051683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-50516832016-10-27 Mapping Long-Term Functional Changes in Cerebral Blood Flow by Arterial Spin Labeling Ssali, Tracy Anazodo, Udunna C. Bureau, Yves MacIntosh, Bradley J. Günther, Matthias St. Lawrence, Keith PLoS One Research Article Although arterial spin labeling (ASL) is appealing for mapping long-term changes in functional activity, inter-sessional variations in basal blood flow, arterial transit times (ATTs), and alignment errors, can result in significant false activation when comparing images from separate sessions. By taking steps to reduce these sources of noise, this study assessed the ability of ASL to detect functional CBF changes between sessions. ASL data were collected in three sessions to image ATT, resting CBF and CBF changes associated with motor activation (7 participants). Activation maps were generated using rest and task images acquired in the same session and from sessions separated by up to a month. Good agreement was found when comparing between-session activation maps to within-session activation maps with only a 16% decrease in precision (within-session: 90 ± 7%) and a 13% decrease in the Dice similarity (within-session: 0.75 ± 0.07) coefficient after a month. In addition, voxel-wise reproducibility (within-session: 4.7 ± 4.5%) and reliability (within-session: 0.89 ± 0.20) of resting grey-matter CBF decreased by less than 18% for the between-session analysis relative to within-session values. ATT variability between sessions (5.0 ± 2.7%) was roughly half the between-subject variability, indicating that its effects on longitudinal CBF were minimal. These results demonstrate that conducting voxel-wise analysis on CBF images acquired on different days is feasible with only modest loss in precision, highlighting the potential of ASL for longitudinal studies. Public Library of Science 2016-10-05 /pmc/articles/PMC5051683/ /pubmed/27706218 http://dx.doi.org/10.1371/journal.pone.0164112 Text en © 2016 Ssali et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Ssali, Tracy Anazodo, Udunna C. Bureau, Yves MacIntosh, Bradley J. Günther, Matthias St. Lawrence, Keith Mapping Long-Term Functional Changes in Cerebral Blood Flow by Arterial Spin Labeling |
title | Mapping Long-Term Functional Changes in Cerebral Blood Flow by Arterial Spin Labeling |
title_full | Mapping Long-Term Functional Changes in Cerebral Blood Flow by Arterial Spin Labeling |
title_fullStr | Mapping Long-Term Functional Changes in Cerebral Blood Flow by Arterial Spin Labeling |
title_full_unstemmed | Mapping Long-Term Functional Changes in Cerebral Blood Flow by Arterial Spin Labeling |
title_short | Mapping Long-Term Functional Changes in Cerebral Blood Flow by Arterial Spin Labeling |
title_sort | mapping long-term functional changes in cerebral blood flow by arterial spin labeling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5051683/ https://www.ncbi.nlm.nih.gov/pubmed/27706218 http://dx.doi.org/10.1371/journal.pone.0164112 |
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