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Altered Resting State in Diabetic Neuropathic Pain
BACKGROUND: The spontaneous component of neuropathic pain (NP) has not been explored sufficiently with neuroimaging techniques, given the difficulty to coax out the brain components that sustain background ongoing pain. Here, we address for the first time the correlates of this component in an fMRI...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638013/ https://www.ncbi.nlm.nih.gov/pubmed/19229326 http://dx.doi.org/10.1371/journal.pone.0004542 |
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author | Cauda, Franco Sacco, Katiuscia Duca, Sergio Cocito, Dario D'Agata, Federico Geminiani, Giuliano C. Canavero, Sergio |
author_facet | Cauda, Franco Sacco, Katiuscia Duca, Sergio Cocito, Dario D'Agata, Federico Geminiani, Giuliano C. Canavero, Sergio |
author_sort | Cauda, Franco |
collection | PubMed |
description | BACKGROUND: The spontaneous component of neuropathic pain (NP) has not been explored sufficiently with neuroimaging techniques, given the difficulty to coax out the brain components that sustain background ongoing pain. Here, we address for the first time the correlates of this component in an fMRI study of a group of eight patients suffering from diabetic neuropathic pain and eight healthy control subjects. Specifically, we studied the functional connectivity that is associated with spontaneous neuropathic pain with spatial independent component analysis (sICA). PRINCIPAL FINDINGS: Functional connectivity analyses revealed a cortical network consisting of two anti-correlated patterns: one includes the left fusiform gyrus, the left lingual gyrus, the left inferior temporal gyrus, the right inferior occipital gyrus, the dorsal anterior cingulate cortex bilaterally, the pre and postcentral gyrus bilaterally, in which its activity is correlated negatively with pain and positively with the controls; the other includes the left precuneus, dorsolateral prefrontal, frontopolar cortex (both bilaterally), right superior frontal gyrus, left inferior frontal gyrus, thalami, both insulae, inferior parietal lobuli, right mammillary body, and a small area in the left brainstem, in which its activity is correlated positively with pain and negatively with the controls. Furthermore, a power spectra analyses revealed group differences in the frequency bands wherein the sICA signal was decomposed: patients' spectra are shifted towards higher frequencies. CONCLUSION: In conclusion, we have characterized here for the first time a functional network of brain areas that mark the spontaneous component of NP. Pain is the result of aberrant default mode functional connectivity. |
format | Text |
id | pubmed-2638013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26380132009-02-20 Altered Resting State in Diabetic Neuropathic Pain Cauda, Franco Sacco, Katiuscia Duca, Sergio Cocito, Dario D'Agata, Federico Geminiani, Giuliano C. Canavero, Sergio PLoS One Research Article BACKGROUND: The spontaneous component of neuropathic pain (NP) has not been explored sufficiently with neuroimaging techniques, given the difficulty to coax out the brain components that sustain background ongoing pain. Here, we address for the first time the correlates of this component in an fMRI study of a group of eight patients suffering from diabetic neuropathic pain and eight healthy control subjects. Specifically, we studied the functional connectivity that is associated with spontaneous neuropathic pain with spatial independent component analysis (sICA). PRINCIPAL FINDINGS: Functional connectivity analyses revealed a cortical network consisting of two anti-correlated patterns: one includes the left fusiform gyrus, the left lingual gyrus, the left inferior temporal gyrus, the right inferior occipital gyrus, the dorsal anterior cingulate cortex bilaterally, the pre and postcentral gyrus bilaterally, in which its activity is correlated negatively with pain and positively with the controls; the other includes the left precuneus, dorsolateral prefrontal, frontopolar cortex (both bilaterally), right superior frontal gyrus, left inferior frontal gyrus, thalami, both insulae, inferior parietal lobuli, right mammillary body, and a small area in the left brainstem, in which its activity is correlated positively with pain and negatively with the controls. Furthermore, a power spectra analyses revealed group differences in the frequency bands wherein the sICA signal was decomposed: patients' spectra are shifted towards higher frequencies. CONCLUSION: In conclusion, we have characterized here for the first time a functional network of brain areas that mark the spontaneous component of NP. Pain is the result of aberrant default mode functional connectivity. Public Library of Science 2009-02-20 /pmc/articles/PMC2638013/ /pubmed/19229326 http://dx.doi.org/10.1371/journal.pone.0004542 Text en Cauda 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Cauda, Franco Sacco, Katiuscia Duca, Sergio Cocito, Dario D'Agata, Federico Geminiani, Giuliano C. Canavero, Sergio Altered Resting State in Diabetic Neuropathic Pain |
title | Altered Resting State in Diabetic Neuropathic Pain |
title_full | Altered Resting State in Diabetic Neuropathic Pain |
title_fullStr | Altered Resting State in Diabetic Neuropathic Pain |
title_full_unstemmed | Altered Resting State in Diabetic Neuropathic Pain |
title_short | Altered Resting State in Diabetic Neuropathic Pain |
title_sort | altered resting state in diabetic neuropathic pain |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638013/ https://www.ncbi.nlm.nih.gov/pubmed/19229326 http://dx.doi.org/10.1371/journal.pone.0004542 |
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