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Somatotopic disruption of the functional connectivity of the primary sensorimotor cortex in complex regional pain syndrome type 1

In complex regional pain syndrome (CRPS), the representation area of the affected limb in the primary sensorimotor cortex (SM1) reacts abnormally during sensory stimulation and motor actions. We recorded 3T functional magnetic resonance imaging resting‐state data from 17 upper‐limb CRPS type 1 patie...

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Autores principales: Hotta, Jaakko, Saari, Jukka, Harno, Hanna, Kalso, Eija, Forss, Nina, Hari, Riitta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619416/
https://www.ncbi.nlm.nih.gov/pubmed/37837646
http://dx.doi.org/10.1002/hbm.26513
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author Hotta, Jaakko
Saari, Jukka
Harno, Hanna
Kalso, Eija
Forss, Nina
Hari, Riitta
author_facet Hotta, Jaakko
Saari, Jukka
Harno, Hanna
Kalso, Eija
Forss, Nina
Hari, Riitta
author_sort Hotta, Jaakko
collection PubMed
description In complex regional pain syndrome (CRPS), the representation area of the affected limb in the primary sensorimotor cortex (SM1) reacts abnormally during sensory stimulation and motor actions. We recorded 3T functional magnetic resonance imaging resting‐state data from 17 upper‐limb CRPS type 1 patients and 19 healthy control subjects to identify alterations of patients' SM1 function during spontaneous pain and to find out how the spatial distribution of these alterations were related to peripheral symptoms. Seed‐based correlations and independent component analyses indicated that patients' upper‐limb SM1 representation areas display (i) reduced interhemispheric connectivity, associated with the combined effect of intensity and spatial extent of limb pain, (ii) increased connectivity with the right anterior insula that positively correlated with the duration of CRPS, (iii) increased connectivity with periaqueductal gray matter, and (iv) disengagement from the other parts of the SM1 network. These findings, now reported for the first time in CRPS, parallel the alterations found in patients suffering from other chronic pain conditions or from limb denervation; they also agree with findings in healthy persons who are exposed to experimental pain or have used their limbs asymmetrically. Our results suggest that CRPS is associated with a sustained and somatotopically specific alteration of SM1 function, that has correspondence to the spatial distribution of the peripheral manifestations and to the duration of the syndrome.
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spelling pubmed-106194162023-11-02 Somatotopic disruption of the functional connectivity of the primary sensorimotor cortex in complex regional pain syndrome type 1 Hotta, Jaakko Saari, Jukka Harno, Hanna Kalso, Eija Forss, Nina Hari, Riitta Hum Brain Mapp Research Articles In complex regional pain syndrome (CRPS), the representation area of the affected limb in the primary sensorimotor cortex (SM1) reacts abnormally during sensory stimulation and motor actions. We recorded 3T functional magnetic resonance imaging resting‐state data from 17 upper‐limb CRPS type 1 patients and 19 healthy control subjects to identify alterations of patients' SM1 function during spontaneous pain and to find out how the spatial distribution of these alterations were related to peripheral symptoms. Seed‐based correlations and independent component analyses indicated that patients' upper‐limb SM1 representation areas display (i) reduced interhemispheric connectivity, associated with the combined effect of intensity and spatial extent of limb pain, (ii) increased connectivity with the right anterior insula that positively correlated with the duration of CRPS, (iii) increased connectivity with periaqueductal gray matter, and (iv) disengagement from the other parts of the SM1 network. These findings, now reported for the first time in CRPS, parallel the alterations found in patients suffering from other chronic pain conditions or from limb denervation; they also agree with findings in healthy persons who are exposed to experimental pain or have used their limbs asymmetrically. Our results suggest that CRPS is associated with a sustained and somatotopically specific alteration of SM1 function, that has correspondence to the spatial distribution of the peripheral manifestations and to the duration of the syndrome. John Wiley & Sons, Inc. 2023-10-14 /pmc/articles/PMC10619416/ /pubmed/37837646 http://dx.doi.org/10.1002/hbm.26513 Text en © 2023 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Hotta, Jaakko
Saari, Jukka
Harno, Hanna
Kalso, Eija
Forss, Nina
Hari, Riitta
Somatotopic disruption of the functional connectivity of the primary sensorimotor cortex in complex regional pain syndrome type 1
title Somatotopic disruption of the functional connectivity of the primary sensorimotor cortex in complex regional pain syndrome type 1
title_full Somatotopic disruption of the functional connectivity of the primary sensorimotor cortex in complex regional pain syndrome type 1
title_fullStr Somatotopic disruption of the functional connectivity of the primary sensorimotor cortex in complex regional pain syndrome type 1
title_full_unstemmed Somatotopic disruption of the functional connectivity of the primary sensorimotor cortex in complex regional pain syndrome type 1
title_short Somatotopic disruption of the functional connectivity of the primary sensorimotor cortex in complex regional pain syndrome type 1
title_sort somatotopic disruption of the functional connectivity of the primary sensorimotor cortex in complex regional pain syndrome type 1
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619416/
https://www.ncbi.nlm.nih.gov/pubmed/37837646
http://dx.doi.org/10.1002/hbm.26513
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