Altered subcortical emotional salience processing differentiates Parkinson's patients with and without psychotic symptoms.


Journal

NeuroImage. Clinical
ISSN: 2213-1582
Titre abrégé: Neuroimage Clin
Pays: Netherlands
ID NLM: 101597070

Informations de publication

Date de publication:
2020
Historique:
received: 28 10 2019
revised: 30 03 2020
accepted: 05 05 2020
pubmed: 17 6 2020
medline: 9 3 2021
entrez: 17 6 2020
Statut: ppublish

Résumé

Current research does not provide a clear explanation for why some patients with Parkinson's Disease (PD) develop psychotic symptoms. The 'aberrant salience hypothesis' of psychosis has been influential and proposes that dopaminergic dysregulation leads to inappropriate attribution of salience to irrelevant/non-informative stimuli, facilitating the formation of hallucinations and delusions. The aim of this study is to investigate whether non-motivational salience is altered in PD patients and possibly linked to the development of psychotic symptoms. We investigated salience processing in 14 PD patients with psychotic symptoms, 23 PD patients without psychotic symptoms and 19 healthy controls. All patients were on dopaminergic medication for their PD. We examined emotional salience using a visual oddball fMRI paradigm that has been used to investigate early stages of schizophrenia spectrum psychosis, controlling for resting cerebral blood flow as assessed with arterial spin labelling fMRI. We found significant differences between patient groups in brain responses to emotional salience. PD patients with psychotic symptoms had enhanced brain responses in the striatum, dopaminergic midbrain, hippocampus and amygdala compared to patients without psychotic symptoms. PD patients with psychotic symptoms showed significant correlations between the levels of dopaminergic drugs they were taking and BOLD signalling, as well as psychotic symptom scores. Our study suggests that enhanced signalling in the striatum, dopaminergic midbrain, the hippocampus and amygdala is associated with the development of psychotic symptoms in PD, in line with that proposed in the 'aberrant salience hypothesis' of psychosis in schizophrenia.

Identifiants

pubmed: 32540629
pii: S2213-1582(20)30114-5
doi: 10.1016/j.nicl.2020.102277
pmc: PMC7298672
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

102277

Subventions

Organisme : Medical Research Council
ID : G0701911
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

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Auteurs

F Knolle (F)

Department of Psychiatry, University of Cambridge, Cambridge, UK; Department of Neuroradiology, Technical University Munich, Munich, Germany. Electronic address: franziska.knolle@tum.de.

S Garofalo (S)

University of Bologna, Department of Psychology, Bologna, Italy.

R Viviani (R)

Institute of Psychology, University of Innsbruck, Innsbruck, Austria; Psychiatry and Psychotherapy Clinic III, University of Ulm, Ulm, Germany.

A Justicia (A)

Department of Psychiatry, University of Cambridge, Cambridge, UK; IMIM (Hospital del Mar Medical Research Institute), Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Barcelona, Spain.

A O Ermakova (AO)

Faculty of Natural Sciences, Imperial College London, UK.

H Blank (H)

Institute of Systems Neuroscience, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

G B Williams (GB)

Department of Clinical Neuroscience and WT-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.

G Arrondo (G)

Department of Psychiatry, University of Cambridge, Cambridge, UK.

P Ramachandra (P)

Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, UK.

C Tudor-Sfetea (C)

Department of Psychiatry, University of Cambridge, Cambridge, UK.

N Bunzeck (N)

Institute of Psychology I, University of Lübeck, Lübeck, Germany.

E Duezel (E)

Otto-von-Guericke University Magdeburg, Institute of Cognitive Neurology and Dementia Research, Magdeburg, Germany; German Centre for Neurodegenerative Diseases (DZNE), Magdeburg, Germany.

T W Robbins (TW)

Department of Psychology, University of Cambridge, Cambridge, UK.

R A Barker (RA)

Department of Clinical Neuroscience and WT-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.

G K Murray (GK)

Department of Psychiatry, University of Cambridge, Cambridge, UK.

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Classifications MeSH