P3a amplitude to trauma-related stimuli reduced after successful trauma-focused PTSD treatment.

Cognitive processing therapy Event-related potential Hyperarousal OIF/OEF/OND veterans Repetitive transcranial magnetic stimulation

Journal

Biological psychology
ISSN: 1873-6246
Titre abrégé: Biol Psychol
Pays: Netherlands
ID NLM: 0375566

Informations de publication

Date de publication:
09 2023
Historique:
received: 24 02 2023
revised: 18 07 2023
accepted: 19 07 2023
medline: 15 9 2023
pubmed: 24 7 2023
entrez: 23 7 2023
Statut: ppublish

Résumé

An elevated P3a amplitude to trauma-related stimuli is strongly associated with posttraumatic stress disorder (PTSD), yet little is known about whether this response to trauma-related stimuli is affected by treatment that decreases PTSD symptoms. As an analysis of secondary outcome measures from a randomized controlled trial, we investigated the latency and amplitude changes of the P3a in responses in a three-condition oddball visual task that included trauma-related (combat scenes) and trauma-unrelated (threatening animals) distractors. Fifty-five U.S. veterans diagnosed with combat-related PTSD were randomized to receive either active or sham repetitive transcranial magnetic stimulation (rTMS). All received cognitive processing therapy, CPT+A, which requires a written account of the index trauma. They were tested before and 6 months after protocol completion. P3a amplitude and response time decreases were driven largely by the changes in the responses to the trauma-related stimuli, and this decrease correlated to the decrease in PTSD symptoms. The amplitude changes were greater in those who received rTMS + CPT than in those who received sham rTMS + CPT, suggesting that rTMS plays beneficial role in reducing arousal and threat bias, which may allow for more effective engagement in trauma-focused PTSD treatment.

Identifiants

pubmed: 37482132
pii: S0301-0511(23)00166-7
doi: 10.1016/j.biopsycho.2023.108648
pii:
doi:

Types de publication

Journal Article Randomized Controlled Trial Research Support, U.S. Gov't, Non-P.H.S. Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

108648

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Gail D Tillman (GD)

Callier Center, University of Texas at Dallas, Dallas, TX, USA. Electronic address: gtillman@utdallas.edu.

Elizabeth Ellen Morris (EE)

Callier Center, University of Texas at Dallas, Dallas, TX, USA.

Christina Bass (C)

Callier Center, University of Texas at Dallas, Dallas, TX, USA.

Mary Turner (M)

Departments of Psychiatry University of Texas Southwestern Medical Center, Dallas, TX, USA.

Kelsey Watson (K)

Callier Center, University of Texas at Dallas, Dallas, TX, USA.

Jared T Brooks (JT)

Callier Center, University of Texas at Dallas, Dallas, TX, USA.

Tyler Rawlinson (T)

Callier Center, University of Texas at Dallas, Dallas, TX, USA.

F Andrew Kozel (FA)

Department of Behavioral Sciences and Social Medicine, Florida State University, Tallahassee, FL, USA.

Michael A Kraut (MA)

Department of Radiology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Michael A Motes (MA)

Callier Center, University of Texas at Dallas, Dallas, TX, USA.

John Hart (J)

Callier Center, University of Texas at Dallas, Dallas, TX, USA; Departments of Psychiatry University of Texas Southwestern Medical Center, Dallas, TX, USA; Departments of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

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Classifications MeSH