Poorer Inhibitory Control Uniquely Contributes to Greater Functional Disability in Post-9/11 Veterans

Abstract Objective Post-9/11 Veterans endorse greater self-reported functional disability than 80% of the adult population. Previous studies of trauma-exposed populations have shown that increased post-traumatic stress disorder (PTSD) and depressive symptoms are consistently associated with greater...

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Veröffentlicht in:Archives of clinical neuropsychology 2023-08, Vol.38 (6), p.944-961
Hauptverfasser: DeGutis, Joseph, Agnoli, Sam, Bernstein, John P K, Jagger-Rickels, Audreyana, Evans, Travis C, Fortier, Catherine B, McGlinchey, Regina E, Milberg, William P, Esterman, Michael
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Sprache:eng
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Zusammenfassung:Abstract Objective Post-9/11 Veterans endorse greater self-reported functional disability than 80% of the adult population. Previous studies of trauma-exposed populations have shown that increased post-traumatic stress disorder (PTSD) and depressive symptoms are consistently associated with greater disability. Additionally, poorer cognitive performance in the domain of executive functions, particularly inhibitory control, has been associated with disability, though it is unclear if this effect is independent of and/or interacts with PTSD and depression. Method Three overlapping samples of n = 582, 297, and 183 combat-deployed post-9/11 Veterans completed comprehensive assessments of executive functions, PTSD and depressive symptoms, and self-reported World Health Organization Disability Assessment Schedule-II (WHODAS II). Results Poorer performance on measures of inhibitory control (Delis-Kaplan Executive Functioning System Color-Word Interference-CWI Test and gradual-onset Continuous Performance Test-gradCPT), but not other executive functions, were significantly associated with greater disability on the WHODAS II (ρ’s = −.13 and −.13, p = .002 and .026, respectively). CWI inhibitory control measures accounted for unique variance in disability after controlling for PTSD and depressive symptoms (R2 change = 0.02, p 
ISSN:1873-5843
0887-6177
1873-5843
DOI:10.1093/arclin/acad012