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A meta-analytic study of experimental and chronic orofacial pain excluding headache disorders

Chronic orofacial pain (COFP) disorders are prevalent and debilitating pain conditions affecting the head, neck and face areas. Neuroimaging studies have reported functional and grey matter abnormalities, but not all the studies have reported consistent findings. Identifying convergent abnormalities...

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Detalles Bibliográficos
Autores principales: Ayoub, Lizbeth J., Seminowicz, David A., Moayedi, Massieh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176551/
https://www.ncbi.nlm.nih.gov/pubmed/30292089
http://dx.doi.org/10.1016/j.nicl.2018.09.018
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author Ayoub, Lizbeth J.
Seminowicz, David A.
Moayedi, Massieh
author_facet Ayoub, Lizbeth J.
Seminowicz, David A.
Moayedi, Massieh
author_sort Ayoub, Lizbeth J.
collection PubMed
description Chronic orofacial pain (COFP) disorders are prevalent and debilitating pain conditions affecting the head, neck and face areas. Neuroimaging studies have reported functional and grey matter abnormalities, but not all the studies have reported consistent findings. Identifying convergent abnormalities across COFPs provides a basis for future hypothesis-driven research aimed at elucidating common CNS mechanisms. Here, we perform three coordinate-based meta-analyses according to PRISMA guidelines to elucidate the central mechanisms of orofacial pain disorders. Specifically, we investigated consistent patterns of: (1) brain function to experimental orofacial pain in healthy subjects, (2) structural and (3) functional brain abnormalities in COFP. We computed our coordinate-based meta-analyses using GingerALE. The experimental pain meta-analysis revealed increased brain activity in bilateral thalami, posterior mid-cingulate cortices, and secondary somatosensory cortices, the right posterior parietal cortex extending to the orofacial region of the right primary somatosensory cortex and the right insula, and decreased activity in the right somatomotor regions. The structural COFP meta-analysis identified consistent higher grey matter volume/concentration in the right ventral thalamus and posterior putamen of COFP patients compared to healthy controls. The functional COFP meta-analysis identified a consistent increase in brain activity in the left medial and posterior thalamus and lesser activity in the left posterior insula in COFP, compared to healthy controls. Overall, these findings provide evidence of brain abnormalities in pain-related regions, namely the thalamus and insula, across different COFP disorders. The convergence of thalamic abnormalities in both structure and function suggest a key role for this region in COFP pathophysiology.
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spelling pubmed-61765512018-10-11 A meta-analytic study of experimental and chronic orofacial pain excluding headache disorders Ayoub, Lizbeth J. Seminowicz, David A. Moayedi, Massieh Neuroimage Clin Regular Article Chronic orofacial pain (COFP) disorders are prevalent and debilitating pain conditions affecting the head, neck and face areas. Neuroimaging studies have reported functional and grey matter abnormalities, but not all the studies have reported consistent findings. Identifying convergent abnormalities across COFPs provides a basis for future hypothesis-driven research aimed at elucidating common CNS mechanisms. Here, we perform three coordinate-based meta-analyses according to PRISMA guidelines to elucidate the central mechanisms of orofacial pain disorders. Specifically, we investigated consistent patterns of: (1) brain function to experimental orofacial pain in healthy subjects, (2) structural and (3) functional brain abnormalities in COFP. We computed our coordinate-based meta-analyses using GingerALE. The experimental pain meta-analysis revealed increased brain activity in bilateral thalami, posterior mid-cingulate cortices, and secondary somatosensory cortices, the right posterior parietal cortex extending to the orofacial region of the right primary somatosensory cortex and the right insula, and decreased activity in the right somatomotor regions. The structural COFP meta-analysis identified consistent higher grey matter volume/concentration in the right ventral thalamus and posterior putamen of COFP patients compared to healthy controls. The functional COFP meta-analysis identified a consistent increase in brain activity in the left medial and posterior thalamus and lesser activity in the left posterior insula in COFP, compared to healthy controls. Overall, these findings provide evidence of brain abnormalities in pain-related regions, namely the thalamus and insula, across different COFP disorders. The convergence of thalamic abnormalities in both structure and function suggest a key role for this region in COFP pathophysiology. Elsevier 2018-09-25 /pmc/articles/PMC6176551/ /pubmed/30292089 http://dx.doi.org/10.1016/j.nicl.2018.09.018 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Ayoub, Lizbeth J.
Seminowicz, David A.
Moayedi, Massieh
A meta-analytic study of experimental and chronic orofacial pain excluding headache disorders
title A meta-analytic study of experimental and chronic orofacial pain excluding headache disorders
title_full A meta-analytic study of experimental and chronic orofacial pain excluding headache disorders
title_fullStr A meta-analytic study of experimental and chronic orofacial pain excluding headache disorders
title_full_unstemmed A meta-analytic study of experimental and chronic orofacial pain excluding headache disorders
title_short A meta-analytic study of experimental and chronic orofacial pain excluding headache disorders
title_sort meta-analytic study of experimental and chronic orofacial pain excluding headache disorders
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176551/
https://www.ncbi.nlm.nih.gov/pubmed/30292089
http://dx.doi.org/10.1016/j.nicl.2018.09.018
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