Associations among epilepsy phenotypes and pain, sleep interference, and dissociative symptoms.
Year: 2026
Type: article
Study design: Observational Study
Abstract: PURPOSE/OBJECTIVE: The current study investigated the extent to which epilepsy comorbidity phenotypes (relatively healthy, posttraumatic stress disorder, polytrauma, bipolar/substance use disorder, chronic disease, and anxiety and depression) are associated with pain interference, sleep interference, and dissociative symptoms for post-9/11 Veterans with epilepsy (VWE). RESEARCH METHOD/DESIGN: A total of 482 veterans were recruited via postal mail with a final sample size of 423 veterans included for analysis, with 59 veterans removed due to incomplete data. Veterans were largely non-Hispanic White (85.80%) and predominantly female (54.80%). Three series of hierarchical blockwise regressions were conducted to test the predictive capability of the epilepsy phenotypes for pain interference, sleep interference, and dissociative symptoms while controlling for covariates (age, ethnicity, sex, traumatic brain injury severity, epilepsy interference, caregiver status, blast exposure, and warzone deployment). RESULTS: < .001), accounting for the largest unique share of variance in pain, sleep, and dissociative symptom scores. CONCLUSION/IMPLICATIONS: Among VWE, some epilepsy phenotypes may account for independent risk beyond demographic and injury characteristics for pain and sleep interference. These findings underscore the importance of targeted assessment and intervention strategies tailored to specific comorbidity profiles in the management of pain and sleep difficulties among VWE. (PsycInfo Database Record (c) 2026 APA, all rights reserved).
Source: Rehabilitation Psychology
DOI: 10.1037/rep0000657
Authors: Jack D. Watson, Elise V. Bailey, Amy Henion, Shirin Saleh, Madeline Myers, Hamada H. Altalib, W. Curt LaFrance, Mary Jo Pugh
Language: English
Subfield: Psychiatry and Mental health
Field: Medicine
Domain: Health Sciences
Open Access status: green
OpenAlex ID: W7130505367
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