Cognitive Behavioral Therapy for Anxiety in Parkinson's Disease Induces Functional Brain Changes.

Parkinson’s disease anxiety cognitive behavioral therapy connectivity fear circuit Trial registration: ClinicalTrials.gov Identifier: NCT02648737

Journal

Journal of Parkinson's disease
ISSN: 1877-718X
Titre abrégé: J Parkinsons Dis
Pays: Netherlands
ID NLM: 101567362

Informations de publication

Date de publication:
2023
Historique:
pubmed: 3 1 2023
medline: 8 2 2023
entrez: 2 1 2023
Statut: ppublish

Résumé

Cognitive behavioral therapy (CBT) reduces anxiety symptoms in patients with Parkinson's disease (PD). The objective of this study was to identify changes in functional connectivity in the brain after CBT for anxiety in patients with PD. Thirty-five patients with PD and clinically significant anxiety were randomized over two groups: CBT plus clinical monitoring (10 CBT sessions) or clinical monitoring only (CMO). Changes in severity of anxiety symptoms were assessed with the Parkinson Anxiety Scale (PAS). Resting-state functional brain MRI was performed at baseline and after the intervention. Functional networks were extracted by an Independent Component Analysis (ICA). Functional connectivity (FC) changes between structures involved in the PD-related anxiety circuits, such as the fear circuit (involving limbic, frontal, and cingulate structures) and the cortico-striato-thalamo-cortical limbic circuit, and both within and between functional networks were compared between groups and regressed with anxiety symptoms changes. Compared to CMO, CBT reduced the FC between the right thalamus and the bilateral orbitofrontal cortices and increased the striato-frontal FC. CBT also increased the fronto-parietal FC within the central executive network (CEN) and between the CEN and the salience network. After CBT, improvement of PAS-score was associated with an increased striato-cingulate and parieto-temporal FC, and a decreased FC within the default-mode network and between the dorsal attentional network and the language network. CBT in PD-patients improves anxiety symptoms and is associated with functional changes reversing the imbalance between PD-related anxiety circuits and reinforcing cognitive control on emotional processing.

Sections du résumé

BACKGROUND
Cognitive behavioral therapy (CBT) reduces anxiety symptoms in patients with Parkinson's disease (PD).
OBJECTIVE
The objective of this study was to identify changes in functional connectivity in the brain after CBT for anxiety in patients with PD.
METHODS
Thirty-five patients with PD and clinically significant anxiety were randomized over two groups: CBT plus clinical monitoring (10 CBT sessions) or clinical monitoring only (CMO). Changes in severity of anxiety symptoms were assessed with the Parkinson Anxiety Scale (PAS). Resting-state functional brain MRI was performed at baseline and after the intervention. Functional networks were extracted by an Independent Component Analysis (ICA). Functional connectivity (FC) changes between structures involved in the PD-related anxiety circuits, such as the fear circuit (involving limbic, frontal, and cingulate structures) and the cortico-striato-thalamo-cortical limbic circuit, and both within and between functional networks were compared between groups and regressed with anxiety symptoms changes.
RESULTS
Compared to CMO, CBT reduced the FC between the right thalamus and the bilateral orbitofrontal cortices and increased the striato-frontal FC. CBT also increased the fronto-parietal FC within the central executive network (CEN) and between the CEN and the salience network. After CBT, improvement of PAS-score was associated with an increased striato-cingulate and parieto-temporal FC, and a decreased FC within the default-mode network and between the dorsal attentional network and the language network.
CONCLUSION
CBT in PD-patients improves anxiety symptoms and is associated with functional changes reversing the imbalance between PD-related anxiety circuits and reinforcing cognitive control on emotional processing.

Identifiants

pubmed: 36591659
pii: JPD223527
doi: 10.3233/JPD-223527
pmc: PMC9912714
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

93-103

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Auteurs

Guillaume Carey (G)

School for Mental Health and Neurosciences, Maastricht University, Maastricht, The Netherlands.
Lille Neuroscience & Cognition, University of Lille, Lille, France.
Department of Neurology and Movement Disorders, Lille University Medical Centre, Lille, France.

Renaud Lopes (R)

Lille Neuroscience & Cognition, University of Lille, Lille, France.
Plateformes Lilloises en Biologie & Santé, University of Lille, Lille, France.

Anja J H Moonen (AJH)

School for Mental Health and Neurosciences, Maastricht University, Maastricht, The Netherlands.
Department of Psychiatry, Maastricht University Medical Centre, Maastricht, The Netherlands.

Anne E P Mulders (AEP)

School for Mental Health and Neurosciences, Maastricht University, Maastricht, The Netherlands.
Department of Psychiatry, Maastricht University Medical Centre, Maastricht, The Netherlands.

Joost J A de Jong (JJA)

School for Mental Health and Neurosciences, Maastricht University, Maastricht, The Netherlands.
Department of Radiology and Nuclear Medicine, Maastricht University Medical Centre, Maastricht, The Netherlands.

Gregory Kuchcinski (G)

Lille Neuroscience & Cognition, University of Lille, Lille, France.
Department of Neuroradiology, Lille University Medical Centre, Lille, France.
Plateformes Lilloises en Biologie & Santé, University of Lille, Lille, France.

Luc Defebvre (L)

Lille Neuroscience & Cognition, University of Lille, Lille, France.
Department of Neurology and Movement Disorders, Lille University Medical Centre, Lille, France.

Mark L Kuijf (ML)

School for Mental Health and Neurosciences, Maastricht University, Maastricht, The Netherlands.
Department of Neurology, Maastricht University Medical Centre, Maastricht, The Netherlands.

Kathy Dujardin (K)

Lille Neuroscience & Cognition, University of Lille, Lille, France.
Department of Neurology and Movement Disorders, Lille University Medical Centre, Lille, France.

Albert F G Leentjens (AFG)

School for Mental Health and Neurosciences, Maastricht University, Maastricht, The Netherlands.
Department of Psychiatry, Maastricht University Medical Centre, Maastricht, The Netherlands.

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Classifications MeSH