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The BOLD signal and neurovascular coupling in autism

BOLD (blood oxygen level dependent) fMRI (functional magnetic resonance imaging) is commonly used to study differences in neuronal activity between human populations. As the BOLD response is an indirect measure of neuronal activity, meaningful interpretation of differences in BOLD responses between...

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Detalles Bibliográficos
Autores principales: Reynell, Clare, Harris, Julia J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3989023/
https://www.ncbi.nlm.nih.gov/pubmed/23917518
http://dx.doi.org/10.1016/j.dcn.2013.07.003
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author Reynell, Clare
Harris, Julia J.
author_facet Reynell, Clare
Harris, Julia J.
author_sort Reynell, Clare
collection PubMed
description BOLD (blood oxygen level dependent) fMRI (functional magnetic resonance imaging) is commonly used to study differences in neuronal activity between human populations. As the BOLD response is an indirect measure of neuronal activity, meaningful interpretation of differences in BOLD responses between groups relies upon a stable relationship existing between neuronal activity and the BOLD response across these groups. However, this relationship can be altered by changes in neurovascular coupling or energy consumption, which would lead to problems in identifying differences in neuronal activity. In this review, we focus on fMRI studies of people with autism, and comparisons that are made of their BOLD responses with those of control groups. We examine neurophysiological differences in autism that may alter neurovascular coupling or energy use, discuss recent studies that have used fMRI to identify differences between participants with autism and control participants, and explore experimental approaches that could help attribute between-group differences in BOLD signals to either neuronal or neurovascular factors.
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spelling pubmed-39890232014-04-17 The BOLD signal and neurovascular coupling in autism Reynell, Clare Harris, Julia J. Dev Cogn Neurosci Review BOLD (blood oxygen level dependent) fMRI (functional magnetic resonance imaging) is commonly used to study differences in neuronal activity between human populations. As the BOLD response is an indirect measure of neuronal activity, meaningful interpretation of differences in BOLD responses between groups relies upon a stable relationship existing between neuronal activity and the BOLD response across these groups. However, this relationship can be altered by changes in neurovascular coupling or energy consumption, which would lead to problems in identifying differences in neuronal activity. In this review, we focus on fMRI studies of people with autism, and comparisons that are made of their BOLD responses with those of control groups. We examine neurophysiological differences in autism that may alter neurovascular coupling or energy use, discuss recent studies that have used fMRI to identify differences between participants with autism and control participants, and explore experimental approaches that could help attribute between-group differences in BOLD signals to either neuronal or neurovascular factors. Elsevier 2013-07-12 /pmc/articles/PMC3989023/ /pubmed/23917518 http://dx.doi.org/10.1016/j.dcn.2013.07.003 Text en © 2013 Elsevier Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Reynell, Clare
Harris, Julia J.
The BOLD signal and neurovascular coupling in autism
title The BOLD signal and neurovascular coupling in autism
title_full The BOLD signal and neurovascular coupling in autism
title_fullStr The BOLD signal and neurovascular coupling in autism
title_full_unstemmed The BOLD signal and neurovascular coupling in autism
title_short The BOLD signal and neurovascular coupling in autism
title_sort bold signal and neurovascular coupling in autism
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3989023/
https://www.ncbi.nlm.nih.gov/pubmed/23917518
http://dx.doi.org/10.1016/j.dcn.2013.07.003
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