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Neural basis of induced phantom limb pain relief

OBJECTIVE: Phantom limb pain (PLP) is notoriously difficult to treat, partly due to an incomplete understanding of PLP‐related disease mechanisms. Noninvasive brain stimulation (NIBS) is used to modulate plasticity in various neuropathological diseases, including chronic pain. Although NIBS can alle...

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Autores principales: Kikkert, Sanne, Mezue, Melvin, O'Shea, Jacinta, Henderson Slater, David, Johansen‐Berg, Heidi, Tracey, Irene, Makin, Tamar R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492189/
https://www.ncbi.nlm.nih.gov/pubmed/30383312
http://dx.doi.org/10.1002/ana.25371
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author Kikkert, Sanne
Mezue, Melvin
O'Shea, Jacinta
Henderson Slater, David
Johansen‐Berg, Heidi
Tracey, Irene
Makin, Tamar R.
author_facet Kikkert, Sanne
Mezue, Melvin
O'Shea, Jacinta
Henderson Slater, David
Johansen‐Berg, Heidi
Tracey, Irene
Makin, Tamar R.
author_sort Kikkert, Sanne
collection PubMed
description OBJECTIVE: Phantom limb pain (PLP) is notoriously difficult to treat, partly due to an incomplete understanding of PLP‐related disease mechanisms. Noninvasive brain stimulation (NIBS) is used to modulate plasticity in various neuropathological diseases, including chronic pain. Although NIBS can alleviate neuropathic pain (including PLP), both disease and treatment mechanisms remain tenuous. Insight into the mechanisms underlying both PLP and NIBS‐induced PLP relief is needed for future implementation of such treatment and generalization to related conditions. METHODS: We used a within‐participants, double‐blind, and sham‐controlled design to alleviate PLP via task‐concurrent NIBS over the primary sensorimotor missing hand cortex (S1/M1). To specifically influence missing hand signal processing, amputees performed phantom hand movements during anodal transcranial direct current stimulation. Brain activity was monitored using neuroimaging during and after NIBS. PLP ratings were obtained throughout the week after stimulation. RESULTS: A single session of intervention NIBS significantly relieved PLP, with effects lasting at least 1 week. PLP relief associated with reduced activity in the S1/M1 missing hand cortex after stimulation. Critically, PLP relief and reduced S1/M1 activity correlated with preceding activity changes during stimulation in the mid‐ and posterior insula and secondary somatosensory cortex (S2). INTERPRETATION: The observed correlation between PLP relief and decreased S1/M1 activity confirms our previous findings linking PLP with increased S1/M1 activity. Our results further highlight the driving role of the mid‐ and posterior insula, as well as S2, in modulating PLP. Lastly, our novel PLP intervention using task‐concurrent NIBS opens new avenues for developing treatment for PLP and related pain conditions. ANN NEUROL 2019;85:59–73.
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spelling pubmed-64921892019-05-07 Neural basis of induced phantom limb pain relief Kikkert, Sanne Mezue, Melvin O'Shea, Jacinta Henderson Slater, David Johansen‐Berg, Heidi Tracey, Irene Makin, Tamar R. Ann Neurol Research Articles OBJECTIVE: Phantom limb pain (PLP) is notoriously difficult to treat, partly due to an incomplete understanding of PLP‐related disease mechanisms. Noninvasive brain stimulation (NIBS) is used to modulate plasticity in various neuropathological diseases, including chronic pain. Although NIBS can alleviate neuropathic pain (including PLP), both disease and treatment mechanisms remain tenuous. Insight into the mechanisms underlying both PLP and NIBS‐induced PLP relief is needed for future implementation of such treatment and generalization to related conditions. METHODS: We used a within‐participants, double‐blind, and sham‐controlled design to alleviate PLP via task‐concurrent NIBS over the primary sensorimotor missing hand cortex (S1/M1). To specifically influence missing hand signal processing, amputees performed phantom hand movements during anodal transcranial direct current stimulation. Brain activity was monitored using neuroimaging during and after NIBS. PLP ratings were obtained throughout the week after stimulation. RESULTS: A single session of intervention NIBS significantly relieved PLP, with effects lasting at least 1 week. PLP relief associated with reduced activity in the S1/M1 missing hand cortex after stimulation. Critically, PLP relief and reduced S1/M1 activity correlated with preceding activity changes during stimulation in the mid‐ and posterior insula and secondary somatosensory cortex (S2). INTERPRETATION: The observed correlation between PLP relief and decreased S1/M1 activity confirms our previous findings linking PLP with increased S1/M1 activity. Our results further highlight the driving role of the mid‐ and posterior insula, as well as S2, in modulating PLP. Lastly, our novel PLP intervention using task‐concurrent NIBS opens new avenues for developing treatment for PLP and related pain conditions. ANN NEUROL 2019;85:59–73. John Wiley and Sons Inc. 2019-01-07 2019-01 /pmc/articles/PMC6492189/ /pubmed/30383312 http://dx.doi.org/10.1002/ana.25371 Text en © 2018 The Authors. Annals of Neurology published by Wiley Periodicals, Inc. on behalf of American Neurological Association. This is an open access article under the terms of the http://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
Kikkert, Sanne
Mezue, Melvin
O'Shea, Jacinta
Henderson Slater, David
Johansen‐Berg, Heidi
Tracey, Irene
Makin, Tamar R.
Neural basis of induced phantom limb pain relief
title Neural basis of induced phantom limb pain relief
title_full Neural basis of induced phantom limb pain relief
title_fullStr Neural basis of induced phantom limb pain relief
title_full_unstemmed Neural basis of induced phantom limb pain relief
title_short Neural basis of induced phantom limb pain relief
title_sort neural basis of induced phantom limb pain relief
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492189/
https://www.ncbi.nlm.nih.gov/pubmed/30383312
http://dx.doi.org/10.1002/ana.25371
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