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Journal article

Neural basis of induced phantom limb pain relief

Abstract:

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.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1002/ana.25371

Authors


More by this author
Role:
Author
ORCID:
0000-0001-9952-4864
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
ORCID:
0000-0002-6007-0698
More by this author
Institution:
University of Oxford
Division:
Medical Sciences Division
Department:
NDORMS
Role:
Author
More by this author
Institution:
University of Oxford
Division:
Medical Sciences Division
Department:
Clinical Neurosciences
Role:
Author


More from this funder
Funding agency for:
Tracey, I
Grant:
Strategic Award
More from this funder
Funding agency for:
Johansen-Berg, H
Tracey, I
Makin, TR
Grant:
110027/Z/15/Z
Strategic Award
104128/Z/14/Z
More from this funder
Funding agency for:
O'Shea, J
Makin, TR
Grant:
Dorothy Hodgkin Fellowship
104128/Z/14/Z


Publisher:
Wiley
Journal:
Annals of Neurology More from this journal
Volume:
85
Issue:
1
Pages:
59-73
Publication date:
2018-11-01
Acceptance date:
2018-10-29
DOI:
EISSN:
1531-8249
ISSN:
0364-5134
Pmid:
30383312


Language:
English
Pubs id:
pubs:936576
UUID:
uuid:efddf56d-6539-478a-8067-0b62f3681b6e
Local pid:
pubs:936576
Source identifiers:
936576
Deposit date:
2018-11-12

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