Central Neuropathic Pain in Multiple Sclerosis Is Associated with Impaired Innocuous Thermal Pathways and Neuronal Hyperexcitability.


Journal

Pain medicine (Malden, Mass.)
ISSN: 1526-4637
Titre abrégé: Pain Med
Pays: England
ID NLM: 100894201

Informations de publication

Date de publication:
08 10 2021
Historique:
pubmed: 19 3 2021
medline: 25 2 2023
entrez: 18 3 2021
Statut: ppublish

Résumé

About one-third of patients with multiple sclerosis (MS) suffers from chronic and excruciating central neuropathic pain (CNP). The mechanism underlying CNP in MS is not clear, since previous studies are scarce and their results are inconsistent. Our aim was to determine whether CNP in MS is associated with impairment of the spinothalamic-thalamocortical pathways (STTCs) and/or increased excitability of the pain system. The study was cross-sectional. The study was conducted at a general hospital. Participants were 47 MS patients with CNP, 42 MS patients without CNP and 32 healthy controls. Sensory testing included the measurement of temperature, pain, and touch thresholds and the thermal grill illusion for evaluating STTCs function and hyperpathia and allodynia as indicators of hyperexcitability. CNP was characterized using interviews and questionnaires. The CNP group had higher cold and warm thresholds (P < 0.01), as well as higher thermal grill illusion perception thresholds (P < 0.05), especially in painful body regions compared with controls, whereas touch and pain thresholds values were normal. The CNP group also had a significantly greater prevalence of hyperpathia and allodynia. Regression analysis revealed that whereas presence of CNP was associated with a higher cold threshold, CNP intensity and the number of painful body regions were associated with allodynia and hyperpathia, respectively. CNP in MS is characterized by a specific impairment of STTC function, the innocuous thermal pathways, and by pain hyperexcitability. Whereas CNP presence is associated with STTC impairment, its severity and extent are associated with pain hyperexcitability. Interventions that reduce excitability level may therefore mitigate CNP severity.

Identifiants

pubmed: 33734398
pii: 6178011
doi: 10.1093/pm/pnab103
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2311-2323

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the American Academy of Pain Medicine. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Michal Rivel (M)

Department of Physical Therapy, School of Health Professions, Sackler Faculty of Medicine Tel Aviv University, Israel.
Sagol School of Neuroscience, Tel-Aviv University, Israel.

Anat Achiron (A)

Multiple Sclerosis Center, Sheba Medical Center, Tel Hashomer, Israel.
Sackler Faculty of Medicine, Tel-Aviv University, Israel.

Mark Dolev (M)

Multiple Sclerosis Center, Sheba Medical Center, Tel Hashomer, Israel.

Yael Stern (Y)

Multiple Sclerosis Center, Sheba Medical Center, Tel Hashomer, Israel.

Gabi Zeilig (G)

Sackler Faculty of Medicine, Tel-Aviv University, Israel.
Department of Neurological Rehabilitation, Sheba Medical Center, Tel Hashomer, Israel.

Ruth Defrin (R)

Department of Physical Therapy, School of Health Professions, Sackler Faculty of Medicine Tel Aviv University, Israel.
Sagol School of Neuroscience, Tel-Aviv University, Israel.

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