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Impact of cognitive behavioural therapy on neural, inflammatory, & autonomic markers in a sample with PTSD and cardiovascular risk: protocol for a pilot randomised controlled trial.
Ellis, Robyn; Sinnott, Sinead; Karam, Krystel; Assefa, Alula; Osborne, Michael; Seligowski, Antonia.
Afiliação
  • Ellis R; Department of Psychiatry, Harvard Medical School, Boston, MA, USA.
  • Sinnott S; McLean Hospital, Belmont, MA, USA.
  • Karam K; Department of Psychiatry, Harvard Medical School, Boston, MA, USA.
  • Assefa A; McLean Hospital, Belmont, MA, USA.
  • Osborne M; Cardiovascular Imaging Research Center, Massachusetts General Hospital, Boston, MA, USA.
  • Seligowski A; Cardiology Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Eur J Psychotraumatol ; 15(1): 2378618, 2024.
Article em En | MEDLINE | ID: mdl-39045795
ABSTRACT

Background:

Individuals with posttraumatic stress disorder (PTSD) are at heightened risk for cardiovascular disease (CVD) compared to the general population. Inflammation and autonomic dysfunction are candidate mechanisms of CVD risk in PTSD; however, these mechanisms have not been well-characterised in the PTSD-CVD link. Further, these mechanisms may operate through altered stress-related neural activity (SNA). Yet, it remains unknown if changes in PTSD are associated with changes in CVD risk mechanisms.

Objective:

This manuscript describes the design and procedures of a pilot randomised controlled trial to assess the impact of a first-line treatment for PTSD (Cognitive Processing Therapy; CPT) versus waitlist control on mechanisms of CVD risk. Further, this study will test the hypothesis that CPT reduces CVD risk through its effects on inflammation and autonomic function and that these changes are driven by changes in SNA.

Methods:

Adults with PTSD and CVD risk (N = 30) will be randomised to CPT or waitlist control. Participants complete two laboratory visits (baseline and post-treatment) that include surveys, brain and peripheral imaging via 18F-fluorodeoxyglucose positron emission tomography (FDG-PET), and resting measures of autonomic function. Primary outcomes include arterial inflammation and heart rate variability. Secondary outcomes include leukopoiesis (bone marrow uptake), heart rate, and blood pressure. The indirect effects of PTSD treatment on changes in inflammation and autonomic function through SNA will also be examined.

Conclusions:

This study seeks to characterise candidate neuroimmune mechanisms of the PTSD-CVD link to identify treatment targets and develop personalised interventions to reduce CVD events in PTSD populations.Trial registration ClinicalTrials.gov identifier NCT06429293..
Individuals with posttraumatic stress disorder (PTSD) have greater risk for cardiovascular disease (CVD) than the general population.Autonomic dysfunction and inflammation are candidate mechanisms of the PTSD-CVD link, which may be driven by changes in neural activity.This pilot randomised controlled trial will test the impact of a first-line PTSD treatment on autonomic dysfunction and inflammation, and whether neural alterations are associated with changes in these mechanisms.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos de Estresse Pós-Traumáticos / Doenças Cardiovasculares / Terapia Cognitivo-Comportamental Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Psychotraumatol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos de Estresse Pós-Traumáticos / Doenças Cardiovasculares / Terapia Cognitivo-Comportamental Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Psychotraumatol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA