Chronic Pain, Perceived Stress, and Cellular Aging: An Exploratory Study

Author:

Sibille Kimberly T1,Langaee Taimour2,Burkley Ben2,Gong Yan2,Glover Toni L3,King Chris1,Riley Joseph L1,Leeuwenburgh Christiaan4,Staud Roland4,Bradley Laurence A5,Fillingim Roger B6

Affiliation:

1. College of Dentistry, University of Florida, P.O. Box 103628, Gainesville, FL 32610-3628, USA

2. College of Pharmacy and Center for Pharmacogenomics, University of Florida, Gainesville, USA

3. College of Dentistry and College of Nursing, University of Florida, Gainesville, USA

4. College of Medicine, University of Florida, Gainesville, USA

5. Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, USA

6. College of Dentistry, University of Florida and North Florida/South Georgia Veterans Health System, Gainesville, USA

Abstract

Background: Chronic pain conditions are characterized by significant individual variability complicating the identification of pathophysiological markers. Leukocyte telomere length (TL), a measure of cellular aging, is associated with age-related disease onset, psychosocial stress, and health-related functional decline. Psychosocial stress has been associated with the onset of chronic pain and chronic pain is experienced as a physical and psychosocial stressor. However, the utility of TL as a biological marker reflecting the burden of chronic pain and psychosocial stress has not yet been explored. Findings: The relationship between chronic pain, stress, and TL was analyzed in 36 ethnically diverse, older adults, half of whom reported no chronic pain and the other half had chronic knee osteoarthritis (OA) pain. Subjects completed a physical exam, radiographs, health history, and psychosocial questionnaires. Blood samples were collected and TL was measured by quantitative polymerase chain reaction (qPCR). Four groups were identified characterized by pain status and the Perceived Stress Scale scores: 1) no pain/low stress, 2) no pain/high stress, chronic pain/low stress, and 4) chronic pain/high stress. TL differed between the pain/stress groups ( p = 0.01), controlling for relevant covariates. Specifically, the chronic pain/high stress group had significantly shorter TL compared to the no pain/low stress group. Age was negatively correlated with TL, particularly in the chronic pain/high stress group ( p = 0.03). Conclusions: Although preliminary in nature and based on a modest sample size, these findings indicate that cellular aging may be more pronounced in older adults experiencing high levels of perceived stress and chronic pain.

Publisher

SAGE Publications

Subject

Anesthesiology and Pain Medicine,Cellular and Molecular Neuroscience,Molecular Medicine

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