Anxiety in Parkinson's Disease Is Associated with Changes in Brain Structural Connectivity.


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:
medline: 12 9 2023
pubmed: 21 8 2023
entrez: 21 8 2023
Statut: ppublish

Résumé

Anxiety in Parkinson's disease (PD) has been associated with grey matter changes and functional changes in anxiety-related neuronal circuits. So far, no study has analyzed white matter (WM) changes in patients with PD and anxiety. The aim of this study was to identify WM changes by comparing PD patients with and without anxiety, using diffusion-tensor imaging (DTI). 108 non-demented PD patients with (n = 31) and without (n = 77) anxiety as defined by their score on the Parkinson Anxiety Scale participated. DTI was used to determine the fractional anisotropy (FA) and mean diffusivity (MD) in specific tracts within anxiety-related neuronal circuits. Mean FA and MD were compared between groups and correlated with the severity of anxiety adjusted by sex, center, Hoehn & Yahr stage, levodopa equivalent daily dosage, and Hamilton depression rating scale. Compared to patients without anxiety, PD patients with anxiety showed lower FA within the striato-orbitofrontal, striato-cingulate, cingulate-limbic, and caudate-thalamic tracts; higher FA within the striato-limbic and accumbens-thalamic tracts; higher MD within the striato-thalamic tract and lower MD within the striato-limbic tract. Anxiety in PD is associated with microstructural alterations in anxiety-related neuronal circuits within the WM. This result reinforces the view that PD-related anxiety is linked to structural alteration within the anxiety-related brain circuits.

Sections du résumé

BACKGROUND
Anxiety in Parkinson's disease (PD) has been associated with grey matter changes and functional changes in anxiety-related neuronal circuits. So far, no study has analyzed white matter (WM) changes in patients with PD and anxiety.
OBJECTIVE
The aim of this study was to identify WM changes by comparing PD patients with and without anxiety, using diffusion-tensor imaging (DTI).
METHODS
108 non-demented PD patients with (n = 31) and without (n = 77) anxiety as defined by their score on the Parkinson Anxiety Scale participated. DTI was used to determine the fractional anisotropy (FA) and mean diffusivity (MD) in specific tracts within anxiety-related neuronal circuits. Mean FA and MD were compared between groups and correlated with the severity of anxiety adjusted by sex, center, Hoehn & Yahr stage, levodopa equivalent daily dosage, and Hamilton depression rating scale.
RESULTS
Compared to patients without anxiety, PD patients with anxiety showed lower FA within the striato-orbitofrontal, striato-cingulate, cingulate-limbic, and caudate-thalamic tracts; higher FA within the striato-limbic and accumbens-thalamic tracts; higher MD within the striato-thalamic tract and lower MD within the striato-limbic tract.
CONCLUSIONS
Anxiety in PD is associated with microstructural alterations in anxiety-related neuronal circuits within the WM. This result reinforces the view that PD-related anxiety is linked to structural alteration within the anxiety-related brain circuits.

Identifiants

pubmed: 37599537
pii: JPD230035
doi: 10.3233/JPD-230035
pmc: PMC10578283
doi:

Substances chimiques

Levodopa 46627O600J

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

989-998

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Auteurs

Guillaume Carey (G)

Univ. Lille, Inserm, CHU Lille, U1172 - LilNCog - Lille Neuroscience & Cognition, Lille, France.
School for Mental Health and Neurosciences (MHeNS), Maastricht University, Maastricht, The Netherlands.
Department of Neurology and Movement Disorders, Lille University Medical Centre, Lille, France.

Romain Viard (R)

Univ Lille, UMS 2014 - US 41 - PLBS - Plateformes Lilloises en Biologie & Santé, Lille, France.

Renaud Lopes (R)

Univ. Lille, Inserm, CHU Lille, U1172 - LilNCog - Lille Neuroscience & Cognition, Lille, France.
Univ Lille, UMS 2014 - US 41 - PLBS - Plateformes Lilloises en Biologie & Santé, Lille, France.

Gregory Kuchcinski (G)

Univ. Lille, Inserm, CHU Lille, U1172 - LilNCog - Lille Neuroscience & Cognition, Lille, France.
Univ Lille, UMS 2014 - US 41 - PLBS - Plateformes Lilloises en Biologie & Santé, Lille, France.
Department of Neuroradiology, Lille University Medical Centre, Lille, France.

Luc Defebvre (L)

Univ. Lille, Inserm, CHU Lille, U1172 - LilNCog - Lille Neuroscience & Cognition, 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 (MHeNS), Maastricht University, Maastricht, The Netherlands.
Department of Psychiatry, Maastricht University Medical Centre, Maastricht, The Netherlands.

Kathy Dujardin (K)

Univ. Lille, Inserm, CHU Lille, U1172 - LilNCog - Lille Neuroscience & Cognition, Lille, France.
Department of Neurology and Movement Disorders, Lille University Medical Centre, Lille, France.

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