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Evoked itch perception is associated with changes in functional brain connectivity
Chronic itch, a highly debilitating condition, has received relatively little attention in the neuroimaging literature. Recent studies suggest that brain regions supporting itch in chronic itch patients encompass sensorimotor and salience networks, and corticostriatal circuits involved in motor prep...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300003/ https://www.ncbi.nlm.nih.gov/pubmed/25610783 http://dx.doi.org/10.1016/j.nicl.2014.12.002 |
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author | Desbordes, Gaëlle Li, Ang Loggia, Marco L. Kim, Jieun Schalock, Peter C. Lerner, Ethan Tran, Thanh N. Ring, Johannes Rosen, Bruce R. Kaptchuk, Ted J. Pfab, Florian Napadow, Vitaly |
author_facet | Desbordes, Gaëlle Li, Ang Loggia, Marco L. Kim, Jieun Schalock, Peter C. Lerner, Ethan Tran, Thanh N. Ring, Johannes Rosen, Bruce R. Kaptchuk, Ted J. Pfab, Florian Napadow, Vitaly |
author_sort | Desbordes, Gaëlle |
collection | PubMed |
description | Chronic itch, a highly debilitating condition, has received relatively little attention in the neuroimaging literature. Recent studies suggest that brain regions supporting itch in chronic itch patients encompass sensorimotor and salience networks, and corticostriatal circuits involved in motor preparation for scratching. However, how these different brain areas interact with one another in the context of itch is still unknown. We acquired BOLD fMRI scans in 14 atopic dermatitis patients to investigate resting-state functional connectivity before and after allergen-induced itch exacerbated the clinical itch perception in these patients. A seed-based analysis revealed decreased functional connectivity from baseline resting state to the evoked-itch state between several itch-related brain regions, particularly the insular and cingulate cortices and basal ganglia, where decreased connectivity was significantly correlated with increased levels of perceived itch. In contrast, evoked itch increased connectivity between key nodes of the frontoparietal control network (superior parietal lobule and dorsolateral prefrontal cortex), where higher increase in connectivity was correlated with a lesser increase in perceived itch, suggesting that greater interaction between nodes of this executive attention network serves to limit itch sensation via enhanced top-down regulation. Overall, our results provide the first evidence of itch-dependent changes in functional connectivity across multiple brain regions. |
format | Online Article Text |
id | pubmed-4300003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-43000032015-01-21 Evoked itch perception is associated with changes in functional brain connectivity Desbordes, Gaëlle Li, Ang Loggia, Marco L. Kim, Jieun Schalock, Peter C. Lerner, Ethan Tran, Thanh N. Ring, Johannes Rosen, Bruce R. Kaptchuk, Ted J. Pfab, Florian Napadow, Vitaly Neuroimage Clin Regular Article Chronic itch, a highly debilitating condition, has received relatively little attention in the neuroimaging literature. Recent studies suggest that brain regions supporting itch in chronic itch patients encompass sensorimotor and salience networks, and corticostriatal circuits involved in motor preparation for scratching. However, how these different brain areas interact with one another in the context of itch is still unknown. We acquired BOLD fMRI scans in 14 atopic dermatitis patients to investigate resting-state functional connectivity before and after allergen-induced itch exacerbated the clinical itch perception in these patients. A seed-based analysis revealed decreased functional connectivity from baseline resting state to the evoked-itch state between several itch-related brain regions, particularly the insular and cingulate cortices and basal ganglia, where decreased connectivity was significantly correlated with increased levels of perceived itch. In contrast, evoked itch increased connectivity between key nodes of the frontoparietal control network (superior parietal lobule and dorsolateral prefrontal cortex), where higher increase in connectivity was correlated with a lesser increase in perceived itch, suggesting that greater interaction between nodes of this executive attention network serves to limit itch sensation via enhanced top-down regulation. Overall, our results provide the first evidence of itch-dependent changes in functional connectivity across multiple brain regions. Elsevier 2014-12-03 /pmc/articles/PMC4300003/ /pubmed/25610783 http://dx.doi.org/10.1016/j.nicl.2014.12.002 Text en © 2014 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Regular Article Desbordes, Gaëlle Li, Ang Loggia, Marco L. Kim, Jieun Schalock, Peter C. Lerner, Ethan Tran, Thanh N. Ring, Johannes Rosen, Bruce R. Kaptchuk, Ted J. Pfab, Florian Napadow, Vitaly Evoked itch perception is associated with changes in functional brain connectivity |
title | Evoked itch perception is associated with changes in functional brain connectivity |
title_full | Evoked itch perception is associated with changes in functional brain connectivity |
title_fullStr | Evoked itch perception is associated with changes in functional brain connectivity |
title_full_unstemmed | Evoked itch perception is associated with changes in functional brain connectivity |
title_short | Evoked itch perception is associated with changes in functional brain connectivity |
title_sort | evoked itch perception is associated with changes in functional brain connectivity |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300003/ https://www.ncbi.nlm.nih.gov/pubmed/25610783 http://dx.doi.org/10.1016/j.nicl.2014.12.002 |
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