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A short, robust brain activation control task optimised for pharmacological fMRI studies

BACKGROUND: Functional magnetic resonance imaging (fMRI) is a popular method for examining pharmacological effects on the brain; however, the BOLD response is dependent on intact neurovascular coupling, and potentially modulated by a number of physiological factors. Pharmacological fMRI is therefore...

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Autores principales: Harvey, Jessica-Lily, Demetriou, Lysia, McGonigle, John, Wall, Matthew B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138041/
https://www.ncbi.nlm.nih.gov/pubmed/30221091
http://dx.doi.org/10.7717/peerj.5540
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author Harvey, Jessica-Lily
Demetriou, Lysia
McGonigle, John
Wall, Matthew B.
author_facet Harvey, Jessica-Lily
Demetriou, Lysia
McGonigle, John
Wall, Matthew B.
author_sort Harvey, Jessica-Lily
collection PubMed
description BACKGROUND: Functional magnetic resonance imaging (fMRI) is a popular method for examining pharmacological effects on the brain; however, the BOLD response is dependent on intact neurovascular coupling, and potentially modulated by a number of physiological factors. Pharmacological fMRI is therefore vulnerable to confounding effects of pharmacological probes on general physiology or neurovascular coupling. Controlling for such non-specific effects in pharmacological fMRI studies is therefore an important consideration, and there is an additional need for well-validated fMRI task paradigms that could be used to control for such effects, or for general testing purposes. METHODS: We have developed two variants of a standardized control task that are short (5 minutes duration) simple (for both the subject and experimenter), widely applicable, and yield a number of readouts in a spatially diverse set of brain networks. The tasks consist of four functionally discrete three-second trial types (plus additional null trials) and contain visual, auditory, motor and cognitive (eye-movements, and working memory tasks in the two task variants) stimuli. Performance of the tasks was assessed in a group of 15 subjects scanned on two separate occasions, with test-retest reliability explicitly assessed using intra-class correlation coefficients. RESULTS: Both tasks produced robust patterns of brain activation in the expected brain regions, and region of interest-derived reliability coefficients for the tasks were generally high, with four out of eight task conditions rated as ‘excellent’ or ‘good’, and only one out of eight rated as ‘poor’. Median values in the voxel-wise reliability measures were also >0.7 for all task conditions, and therefore classed as ‘excellent’ or ‘good’. The spatial concordance between the most highly activated voxels and those with the highest reliability coefficients was greater for the sensory (auditory, visual) conditions than the other (motor, cognitive) conditions. DISCUSSION: Either of the two task variants would be suitable for use as a control task in future pharmacological fMRI studies or for any other investigation where a short, reliable, basic task paradigm is required. Stimulus code is available online for re-use by the scientific community.
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spelling pubmed-61380412018-09-14 A short, robust brain activation control task optimised for pharmacological fMRI studies Harvey, Jessica-Lily Demetriou, Lysia McGonigle, John Wall, Matthew B. PeerJ Neuroscience BACKGROUND: Functional magnetic resonance imaging (fMRI) is a popular method for examining pharmacological effects on the brain; however, the BOLD response is dependent on intact neurovascular coupling, and potentially modulated by a number of physiological factors. Pharmacological fMRI is therefore vulnerable to confounding effects of pharmacological probes on general physiology or neurovascular coupling. Controlling for such non-specific effects in pharmacological fMRI studies is therefore an important consideration, and there is an additional need for well-validated fMRI task paradigms that could be used to control for such effects, or for general testing purposes. METHODS: We have developed two variants of a standardized control task that are short (5 minutes duration) simple (for both the subject and experimenter), widely applicable, and yield a number of readouts in a spatially diverse set of brain networks. The tasks consist of four functionally discrete three-second trial types (plus additional null trials) and contain visual, auditory, motor and cognitive (eye-movements, and working memory tasks in the two task variants) stimuli. Performance of the tasks was assessed in a group of 15 subjects scanned on two separate occasions, with test-retest reliability explicitly assessed using intra-class correlation coefficients. RESULTS: Both tasks produced robust patterns of brain activation in the expected brain regions, and region of interest-derived reliability coefficients for the tasks were generally high, with four out of eight task conditions rated as ‘excellent’ or ‘good’, and only one out of eight rated as ‘poor’. Median values in the voxel-wise reliability measures were also >0.7 for all task conditions, and therefore classed as ‘excellent’ or ‘good’. The spatial concordance between the most highly activated voxels and those with the highest reliability coefficients was greater for the sensory (auditory, visual) conditions than the other (motor, cognitive) conditions. DISCUSSION: Either of the two task variants would be suitable for use as a control task in future pharmacological fMRI studies or for any other investigation where a short, reliable, basic task paradigm is required. Stimulus code is available online for re-use by the scientific community. PeerJ Inc. 2018-09-11 /pmc/articles/PMC6138041/ /pubmed/30221091 http://dx.doi.org/10.7717/peerj.5540 Text en ©2018 Harvey 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, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Neuroscience
Harvey, Jessica-Lily
Demetriou, Lysia
McGonigle, John
Wall, Matthew B.
A short, robust brain activation control task optimised for pharmacological fMRI studies
title A short, robust brain activation control task optimised for pharmacological fMRI studies
title_full A short, robust brain activation control task optimised for pharmacological fMRI studies
title_fullStr A short, robust brain activation control task optimised for pharmacological fMRI studies
title_full_unstemmed A short, robust brain activation control task optimised for pharmacological fMRI studies
title_short A short, robust brain activation control task optimised for pharmacological fMRI studies
title_sort short, robust brain activation control task optimised for pharmacological fmri studies
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138041/
https://www.ncbi.nlm.nih.gov/pubmed/30221091
http://dx.doi.org/10.7717/peerj.5540
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