Chronic Pain is Associated With Reduced Sympathetic Nervous System Reactivity During Simple and Complex Walking Tasks: Potential Cerebral Mechanisms.

central autonomic network chronic pain mobility neuroimaging sympathetic nervous system

Journal

Chronic stress (Thousand Oaks, Calif.)
ISSN: 2470-5470
Titre abrégé: Chronic Stress (Thousand Oaks)
Pays: United States
ID NLM: 101701229

Informations de publication

Date de publication:
Historique:
received: 18 05 2021
accepted: 17 06 2021
entrez: 21 7 2021
pubmed: 22 7 2021
medline: 22 7 2021
Statut: epublish

Résumé

Autonomic dysregulation may lead to blunted sympathetic reactivity in chronic pain states. Autonomic responses are controlled by the central autonomic network (CAN). Little research has examined sympathetic reactivity and associations with brain CAN structures in the presence of chronic pain; thus, the present study aims to investigate how chronic pain influences sympathetic reactivity and associations with CAN brain region volumes. Sympathetic reactivity was measured as change in skin conductance level (ΔSCL) between a resting reference period and walking periods for typical and complex walking tasks (obstacle and dual-task). Participants included 31 people with (n = 19) and without (n = 12) chronic musculoskeletal pain. Structural 3 T MRI was used to determine gray matter volume associations with ΔSCL in regions of the CAN (i.e., brainstem, amygdala, insula, and anterior cingulate cortex). ΔSCL varied across walking tasks (main effect p = 0.036), with lower ΔSCL in chronic pain participants compared to controls across trials 2 and 3 under the obstacle walking condition. ΔSCL during typical walking was associated with multiple CAN gray matter volumes, including brainstem, bilateral insula, amygdala, and right caudal anterior cingulate cortex (p's < 0.05). The difference in ΔSCL from typical-to-obstacle walking were associated with volumes of the midbrain segment of the brainstem and anterior segment of the circular sulcus of the insula (p's < 0.05), with no other significant associations. The difference in ΔSCL from typical-to-dual task walking was associated with the bilateral caudal anterior cingulate cortex, and left rostral cingulate cortex (p's < 0.05). Sympathetic reactivity is blunted during typical and complex walking tasks in persons with chronic pain. Additionally, blunted sympathetic reactivity is associated with CAN brain structure, with direction of association dependent on brain region. These results support the idea that chronic pain may negatively impact typical autonomic responses needed for walking performance via its potential impact on the brain.

Sections du résumé

BACKGROUND BACKGROUND
Autonomic dysregulation may lead to blunted sympathetic reactivity in chronic pain states. Autonomic responses are controlled by the central autonomic network (CAN). Little research has examined sympathetic reactivity and associations with brain CAN structures in the presence of chronic pain; thus, the present study aims to investigate how chronic pain influences sympathetic reactivity and associations with CAN brain region volumes.
METHODS METHODS
Sympathetic reactivity was measured as change in skin conductance level (ΔSCL) between a resting reference period and walking periods for typical and complex walking tasks (obstacle and dual-task). Participants included 31 people with (n = 19) and without (n = 12) chronic musculoskeletal pain. Structural 3 T MRI was used to determine gray matter volume associations with ΔSCL in regions of the CAN (i.e., brainstem, amygdala, insula, and anterior cingulate cortex).
RESULTS RESULTS
ΔSCL varied across walking tasks (main effect p = 0.036), with lower ΔSCL in chronic pain participants compared to controls across trials 2 and 3 under the obstacle walking condition. ΔSCL during typical walking was associated with multiple CAN gray matter volumes, including brainstem, bilateral insula, amygdala, and right caudal anterior cingulate cortex (p's < 0.05). The difference in ΔSCL from typical-to-obstacle walking were associated with volumes of the midbrain segment of the brainstem and anterior segment of the circular sulcus of the insula (p's < 0.05), with no other significant associations. The difference in ΔSCL from typical-to-dual task walking was associated with the bilateral caudal anterior cingulate cortex, and left rostral cingulate cortex (p's < 0.05).
CONCLUSIONS CONCLUSIONS
Sympathetic reactivity is blunted during typical and complex walking tasks in persons with chronic pain. Additionally, blunted sympathetic reactivity is associated with CAN brain structure, with direction of association dependent on brain region. These results support the idea that chronic pain may negatively impact typical autonomic responses needed for walking performance via its potential impact on the brain.

Identifiants

pubmed: 34286166
doi: 10.1177/24705470211030273
pii: 10.1177_24705470211030273
pmc: PMC8267022
doi:

Types de publication

Journal Article

Langues

eng

Pagination

24705470211030273

Subventions

Organisme : NIAMS NIH HHS
ID : F31 AR077996
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR071431
Pays : United States

Informations de copyright

© The Author(s) 2021.

Déclaration de conflit d'intérêts

Declaration of Conflicting Interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

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Auteurs

Taylor D Yeater (TD)

Pain Research & Intervention Center of Excellence, University of Florida, University of Florida, Gainesville, FL, USA.
J. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, University of Florida, Gainesville, FL, USA.

David J Clark (DJ)

Department of Aging and Geriatric Research, University of Florida, University of Florida, Gainesville, FL, USA.
Brain Rehabilitation Research Center, Malcom Randall VA Medical Center, Gainesville, FL, USA.

Lorraine Hoyos (L)

Pain Research & Intervention Center of Excellence, University of Florida, University of Florida, Gainesville, FL, USA.
Department of Aging and Geriatric Research, University of Florida, University of Florida, Gainesville, FL, USA.

Pedro A Valdes-Hernandez (PA)

Pain Research & Intervention Center of Excellence, University of Florida, University of Florida, Gainesville, FL, USA.
Department of Aging and Geriatric Research, University of Florida, University of Florida, Gainesville, FL, USA.
Department of Community Dentistry & Behavioral Sciences, University of Florida, University of Florida, Gainesville, FL, USA.

Julio A Peraza (JA)

Pain Research & Intervention Center of Excellence, University of Florida, University of Florida, Gainesville, FL, USA.

Kyle D Allen (KD)

Pain Research & Intervention Center of Excellence, University of Florida, University of Florida, Gainesville, FL, USA.
J. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, University of Florida, Gainesville, FL, USA.
Department of Orthopedic Surgery and Sports Medicine, University of Florida, College of Medicine, University of Florida, Gainesville, FL, USA.

Yenisel Cruz-Almeida (Y)

Pain Research & Intervention Center of Excellence, University of Florida, University of Florida, Gainesville, FL, USA.
Department of Aging and Geriatric Research, University of Florida, University of Florida, Gainesville, FL, USA.
Department of Community Dentistry & Behavioral Sciences, University of Florida, University of Florida, Gainesville, FL, USA.

Classifications MeSH