Cargando…

Multidimensional pain phenotypes after Traumatic Brain Injury

More than 50% of individuals develop chronic pain following traumatic brain injury (TBI). Research suggests that a significant portion of post-TBI chronic pain conditions is neuropathic in nature, yet the relationship between neuropathic pain, psychological distress, and somatosensory function follo...

Descripción completa

Detalles Bibliográficos
Autores principales: Robayo, Linda E., Govind, Varan, Vastano, Roberta, Felix, Elizabeth R., Fleming, Loriann, Cherup, Nicholas P., Widerström-Noga, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437424/
https://www.ncbi.nlm.nih.gov/pubmed/36061413
http://dx.doi.org/10.3389/fpain.2022.947562
_version_ 1784781607632109568
author Robayo, Linda E.
Govind, Varan
Vastano, Roberta
Felix, Elizabeth R.
Fleming, Loriann
Cherup, Nicholas P.
Widerström-Noga, Eva
author_facet Robayo, Linda E.
Govind, Varan
Vastano, Roberta
Felix, Elizabeth R.
Fleming, Loriann
Cherup, Nicholas P.
Widerström-Noga, Eva
author_sort Robayo, Linda E.
collection PubMed
description More than 50% of individuals develop chronic pain following traumatic brain injury (TBI). Research suggests that a significant portion of post-TBI chronic pain conditions is neuropathic in nature, yet the relationship between neuropathic pain, psychological distress, and somatosensory function following TBI is not fully understood. This study evaluated neuropathic pain symptoms, psychological and somatosensory function, and psychosocial factors in individuals with TBI (TBI, N = 38). A two-step cluster analysis was used to identify phenotypes based on the Neuropathic Pain Symptom Inventory and Beck's Anxiety Inventory scores. Phenotypes were then compared on pain characteristics, psychological and somatosensory function, and psychosocial factors. Our analyses resulted in two different neuropathic pain phenotypes: (1) Moderate neuropathic pain severity and anxiety scores (MNP-AS, N = 11); and (2) mild or no neuropathic pain symptoms and anxiety scores (LNP-AS, N = 27). Furthermore, the MNP-AS group exhibited greater depression, PTSD, pain severity, and affective distress scores than the LNP-AS group. In addition, thermal somatosensory function (difference between thermal pain and perception thresholds) was significantly lower in the MNP-AS compared to the LNP-AS group. Our findings suggest that neuropathic pain symptoms are relatively common after TBI and are not only associated with greater psychosocial distress but also with abnormal function of central pain processing pathways.
format Online
Article
Text
id pubmed-9437424
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-94374242022-09-03 Multidimensional pain phenotypes after Traumatic Brain Injury Robayo, Linda E. Govind, Varan Vastano, Roberta Felix, Elizabeth R. Fleming, Loriann Cherup, Nicholas P. Widerström-Noga, Eva Front Pain Res (Lausanne) Pain Research More than 50% of individuals develop chronic pain following traumatic brain injury (TBI). Research suggests that a significant portion of post-TBI chronic pain conditions is neuropathic in nature, yet the relationship between neuropathic pain, psychological distress, and somatosensory function following TBI is not fully understood. This study evaluated neuropathic pain symptoms, psychological and somatosensory function, and psychosocial factors in individuals with TBI (TBI, N = 38). A two-step cluster analysis was used to identify phenotypes based on the Neuropathic Pain Symptom Inventory and Beck's Anxiety Inventory scores. Phenotypes were then compared on pain characteristics, psychological and somatosensory function, and psychosocial factors. Our analyses resulted in two different neuropathic pain phenotypes: (1) Moderate neuropathic pain severity and anxiety scores (MNP-AS, N = 11); and (2) mild or no neuropathic pain symptoms and anxiety scores (LNP-AS, N = 27). Furthermore, the MNP-AS group exhibited greater depression, PTSD, pain severity, and affective distress scores than the LNP-AS group. In addition, thermal somatosensory function (difference between thermal pain and perception thresholds) was significantly lower in the MNP-AS compared to the LNP-AS group. Our findings suggest that neuropathic pain symptoms are relatively common after TBI and are not only associated with greater psychosocial distress but also with abnormal function of central pain processing pathways. Frontiers Media S.A. 2022-08-19 /pmc/articles/PMC9437424/ /pubmed/36061413 http://dx.doi.org/10.3389/fpain.2022.947562 Text en Copyright © 2022 Robayo, Govind, Vastano, Felix, Fleming, Cherup and Widerström-Noga. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pain Research
Robayo, Linda E.
Govind, Varan
Vastano, Roberta
Felix, Elizabeth R.
Fleming, Loriann
Cherup, Nicholas P.
Widerström-Noga, Eva
Multidimensional pain phenotypes after Traumatic Brain Injury
title Multidimensional pain phenotypes after Traumatic Brain Injury
title_full Multidimensional pain phenotypes after Traumatic Brain Injury
title_fullStr Multidimensional pain phenotypes after Traumatic Brain Injury
title_full_unstemmed Multidimensional pain phenotypes after Traumatic Brain Injury
title_short Multidimensional pain phenotypes after Traumatic Brain Injury
title_sort multidimensional pain phenotypes after traumatic brain injury
topic Pain Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437424/
https://www.ncbi.nlm.nih.gov/pubmed/36061413
http://dx.doi.org/10.3389/fpain.2022.947562
work_keys_str_mv AT robayolindae multidimensionalpainphenotypesaftertraumaticbraininjury
AT govindvaran multidimensionalpainphenotypesaftertraumaticbraininjury
AT vastanoroberta multidimensionalpainphenotypesaftertraumaticbraininjury
AT felixelizabethr multidimensionalpainphenotypesaftertraumaticbraininjury
AT flemingloriann multidimensionalpainphenotypesaftertraumaticbraininjury
AT cherupnicholasp multidimensionalpainphenotypesaftertraumaticbraininjury
AT widerstromnogaeva multidimensionalpainphenotypesaftertraumaticbraininjury