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

Author:

Yeater Taylor D.12ORCID,Clark David J.34,Hoyos Lorraine13,Valdes-Hernandez Pedro A.135,Peraza Julio A.1ORCID,Allen Kyle D.126,Cruz-Almeida Yenisel135

Affiliation:

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

2. J. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, University of Florida, Gainesville, FL, USA

3. Department of Aging and Geriatric Research, University of Florida, University of Florida, Gainesville, FL, USA

4. Brain Rehabilitation Research Center, Malcom Randall VA Medical Center, Gainesville, FL, USA

5. Department of Community Dentistry & Behavioral Sciences, University of Florida, University of Florida, Gainesville, FL, USA

6. Department of Orthopedic Surgery and Sports Medicine, University of Florida, College of Medicine, University of Florida, Gainesville, FL, USA

Abstract

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 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 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 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.

Funder

National Institute on Aging

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Publisher

SAGE Publications

Subject

Behavioral Neuroscience,Biological Psychiatry,Psychiatry and Mental health,Clinical Psychology

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