Cargando…

Sensory phenotypes in complex regional pain syndrome and chronic low back pain—indication of common underlying pathomechanisms

INTRODUCTION: First-line pain treatment is unsatisfactory in more than 50% of chronic pain patients, likely because of the heterogeneity of mechanisms underlying pain chronification. OBJECTIVES: This cross-sectional study aimed to better understand pathomechanisms across different chronic pain cohor...

Descripción completa

Detalles Bibliográficos
Autores principales: De Schoenmacker, Iara, Sirucek, Laura, Scheuren, Paulina S., Lütolf, Robin, Gorrell, Lindsay M., Brunner, Florian, Curt, Armin, Rosner, Jan, Schweinhardt, Petra, Hubli, Michèle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653599/
https://www.ncbi.nlm.nih.gov/pubmed/38027464
http://dx.doi.org/10.1097/PR9.0000000000001110
_version_ 1785147807966953472
author De Schoenmacker, Iara
Sirucek, Laura
Scheuren, Paulina S.
Lütolf, Robin
Gorrell, Lindsay M.
Brunner, Florian
Curt, Armin
Rosner, Jan
Schweinhardt, Petra
Hubli, Michèle
author_facet De Schoenmacker, Iara
Sirucek, Laura
Scheuren, Paulina S.
Lütolf, Robin
Gorrell, Lindsay M.
Brunner, Florian
Curt, Armin
Rosner, Jan
Schweinhardt, Petra
Hubli, Michèle
author_sort De Schoenmacker, Iara
collection PubMed
description INTRODUCTION: First-line pain treatment is unsatisfactory in more than 50% of chronic pain patients, likely because of the heterogeneity of mechanisms underlying pain chronification. OBJECTIVES: This cross-sectional study aimed to better understand pathomechanisms across different chronic pain cohorts, regardless of their diagnoses, by identifying distinct sensory phenotypes through a cluster analysis. METHODS: We recruited 81 chronic pain patients and 63 age-matched and sex-matched healthy controls (HC). Two distinct chronic pain cohorts were recruited, ie, complex regional pain syndrome (N = 20) and low back pain (N = 61). Quantitative sensory testing (QST) was performed in the most painful body area to investigate somatosensory changes related to clinical pain. Furthermore, QST was conducted in a pain-free area to identify remote sensory alterations, indicating more widespread changes in somatosensory processing. RESULTS: Two clusters were identified based on the QST measures in the painful area, which did not represent the 2 distinct pain diagnoses but contained patients from both cohorts. Cluster 1 showed increased pain sensitivities in the painful and control area, indicating central sensitization as a potential pathomechanism. Cluster 2 showed a similar sensory profile as HC in both tested areas. Hence, either QST was not sensitive enough and more objective measures are needed to detect sensitization within the nociceptive neuraxis or cluster 2 may not have pain primarily because of sensitization, but other factors such as psychosocial ones are involved. CONCLUSION: These findings support the notion of shared pathomechanisms irrespective of the pain diagnosis. Conversely, different mechanisms might contribute to the pain of patients with the same diagnosis.
format Online
Article
Text
id pubmed-10653599
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Wolters Kluwer
record_format MEDLINE/PubMed
spelling pubmed-106535992023-11-15 Sensory phenotypes in complex regional pain syndrome and chronic low back pain—indication of common underlying pathomechanisms De Schoenmacker, Iara Sirucek, Laura Scheuren, Paulina S. Lütolf, Robin Gorrell, Lindsay M. Brunner, Florian Curt, Armin Rosner, Jan Schweinhardt, Petra Hubli, Michèle Pain Rep General Section INTRODUCTION: First-line pain treatment is unsatisfactory in more than 50% of chronic pain patients, likely because of the heterogeneity of mechanisms underlying pain chronification. OBJECTIVES: This cross-sectional study aimed to better understand pathomechanisms across different chronic pain cohorts, regardless of their diagnoses, by identifying distinct sensory phenotypes through a cluster analysis. METHODS: We recruited 81 chronic pain patients and 63 age-matched and sex-matched healthy controls (HC). Two distinct chronic pain cohorts were recruited, ie, complex regional pain syndrome (N = 20) and low back pain (N = 61). Quantitative sensory testing (QST) was performed in the most painful body area to investigate somatosensory changes related to clinical pain. Furthermore, QST was conducted in a pain-free area to identify remote sensory alterations, indicating more widespread changes in somatosensory processing. RESULTS: Two clusters were identified based on the QST measures in the painful area, which did not represent the 2 distinct pain diagnoses but contained patients from both cohorts. Cluster 1 showed increased pain sensitivities in the painful and control area, indicating central sensitization as a potential pathomechanism. Cluster 2 showed a similar sensory profile as HC in both tested areas. Hence, either QST was not sensitive enough and more objective measures are needed to detect sensitization within the nociceptive neuraxis or cluster 2 may not have pain primarily because of sensitization, but other factors such as psychosocial ones are involved. CONCLUSION: These findings support the notion of shared pathomechanisms irrespective of the pain diagnosis. Conversely, different mechanisms might contribute to the pain of patients with the same diagnosis. Wolters Kluwer 2023-11-15 /pmc/articles/PMC10653599/ /pubmed/38027464 http://dx.doi.org/10.1097/PR9.0000000000001110 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The International Association for the Study of Pain. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle General Section
De Schoenmacker, Iara
Sirucek, Laura
Scheuren, Paulina S.
Lütolf, Robin
Gorrell, Lindsay M.
Brunner, Florian
Curt, Armin
Rosner, Jan
Schweinhardt, Petra
Hubli, Michèle
Sensory phenotypes in complex regional pain syndrome and chronic low back pain—indication of common underlying pathomechanisms
title Sensory phenotypes in complex regional pain syndrome and chronic low back pain—indication of common underlying pathomechanisms
title_full Sensory phenotypes in complex regional pain syndrome and chronic low back pain—indication of common underlying pathomechanisms
title_fullStr Sensory phenotypes in complex regional pain syndrome and chronic low back pain—indication of common underlying pathomechanisms
title_full_unstemmed Sensory phenotypes in complex regional pain syndrome and chronic low back pain—indication of common underlying pathomechanisms
title_short Sensory phenotypes in complex regional pain syndrome and chronic low back pain—indication of common underlying pathomechanisms
title_sort sensory phenotypes in complex regional pain syndrome and chronic low back pain—indication of common underlying pathomechanisms
topic General Section
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653599/
https://www.ncbi.nlm.nih.gov/pubmed/38027464
http://dx.doi.org/10.1097/PR9.0000000000001110
work_keys_str_mv AT deschoenmackeriara sensoryphenotypesincomplexregionalpainsyndromeandchroniclowbackpainindicationofcommonunderlyingpathomechanisms
AT siruceklaura sensoryphenotypesincomplexregionalpainsyndromeandchroniclowbackpainindicationofcommonunderlyingpathomechanisms
AT scheurenpaulinas sensoryphenotypesincomplexregionalpainsyndromeandchroniclowbackpainindicationofcommonunderlyingpathomechanisms
AT lutolfrobin sensoryphenotypesincomplexregionalpainsyndromeandchroniclowbackpainindicationofcommonunderlyingpathomechanisms
AT gorrelllindsaym sensoryphenotypesincomplexregionalpainsyndromeandchroniclowbackpainindicationofcommonunderlyingpathomechanisms
AT brunnerflorian sensoryphenotypesincomplexregionalpainsyndromeandchroniclowbackpainindicationofcommonunderlyingpathomechanisms
AT curtarmin sensoryphenotypesincomplexregionalpainsyndromeandchroniclowbackpainindicationofcommonunderlyingpathomechanisms
AT rosnerjan sensoryphenotypesincomplexregionalpainsyndromeandchroniclowbackpainindicationofcommonunderlyingpathomechanisms
AT schweinhardtpetra sensoryphenotypesincomplexregionalpainsyndromeandchroniclowbackpainindicationofcommonunderlyingpathomechanisms
AT hublimichele sensoryphenotypesincomplexregionalpainsyndromeandchroniclowbackpainindicationofcommonunderlyingpathomechanisms