La maladie de Parkinson au Canada (serveur d'exploration)

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Salience network and parahippocampal dopamine dysfunction in memory-impaired Parkinson disease.

Identifieur interne : 000568 ( PubMed/Curation ); précédent : 000567; suivant : 000569

Salience network and parahippocampal dopamine dysfunction in memory-impaired Parkinson disease.

Auteurs : Leigh Christopher [Canada] ; Sarah Duff-Canning ; Yuko Koshimori ; Barbara Segura ; Isabelle Boileau ; Robert Chen ; Anthony E. Lang ; Sylvain Houle ; Pablo Rusjan ; Antonio P. Strafella

Source :

RBID : pubmed:25448687

English descriptors

Abstract

Patients with Parkinson disease (PD) and mild cognitive impairment (MCI) are vulnerable to dementia and frequently experience memory deficits. This could be the result of dopamine dysfunction in corticostriatal networks (salience, central executive networks, and striatum) and/or the medial temporal lobe. Our aim was to investigate whether dopamine dysfunction in these regions contributes to memory impairment in PD.

DOI: 10.1002/ana.24323
PubMed: 25448687

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pubmed:25448687

Le document en format XML

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<term>Dopaminergic Neurons (diagnostic imaging)</term>
<term>Dopaminergic Neurons (metabolism)</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Memory Disorders (diagnostic imaging)</term>
<term>Memory Disorders (metabolism)</term>
<term>Middle Aged</term>
<term>Nerve Net (diagnostic imaging)</term>
<term>Nerve Net (metabolism)</term>
<term>Parahippocampal Gyrus (diagnostic imaging)</term>
<term>Parahippocampal Gyrus (metabolism)</term>
<term>Parkinson Disease (diagnostic imaging)</term>
<term>Parkinson Disease (metabolism)</term>
<term>Positron-Emission Tomography (methods)</term>
<term>Protein Binding (physiology)</term>
<term>Receptors, Dopamine D2 (metabolism)</term>
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<term>Parahippocampal Gyrus</term>
<term>Parkinson Disease</term>
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<term>Positron-Emission Tomography</term>
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<div type="abstract" xml:lang="en">Patients with Parkinson disease (PD) and mild cognitive impairment (MCI) are vulnerable to dementia and frequently experience memory deficits. This could be the result of dopamine dysfunction in corticostriatal networks (salience, central executive networks, and striatum) and/or the medial temporal lobe. Our aim was to investigate whether dopamine dysfunction in these regions contributes to memory impairment in PD.</div>
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<Year>2015</Year>
<Month>Feb</Month>
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<Title>Annals of neurology</Title>
<ISOAbbreviation>Ann. Neurol.</ISOAbbreviation>
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<ArticleTitle>Salience network and parahippocampal dopamine dysfunction in memory-impaired Parkinson disease.</ArticleTitle>
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<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">Patients with Parkinson disease (PD) and mild cognitive impairment (MCI) are vulnerable to dementia and frequently experience memory deficits. This could be the result of dopamine dysfunction in corticostriatal networks (salience, central executive networks, and striatum) and/or the medial temporal lobe. Our aim was to investigate whether dopamine dysfunction in these regions contributes to memory impairment in PD.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">We used positron emission tomography imaging to compare D2 receptor availability in the cortex and striatal (limbic and associative) dopamine neuron integrity in 4 groups: memory-impaired PD (amnestic MCI; n = 9), PD with nonamnestic MCI (n = 10), PD without MCI (n = 11), and healthy controls (n = 14). Subjects were administered a full neuropsychological test battery for cognitive performance.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Memory-impaired patients demonstrated more significant reductions in D2 receptor binding in the salience network (insular cortex and anterior cingulate cortex [ACC] and the right parahippocampal gyrus [PHG]) compared to healthy controls and patients with no MCI. They also presented reductions in the right insula and right ACC compared to nonamnestic MCI patients. D2 levels were correlated with memory performance in the right PHG and left insula of amnestic patients and with executive performance in the bilateral insula and left ACC of all MCI patients. Associative striatal dopamine denervation was significant in all PD patients.</AbstractText>
<AbstractText Label="INTERPRETATION" NlmCategory="CONCLUSIONS">Dopaminergic differences in the salience network and the medial temporal lobe contribute to memory impairment in PD. Furthermore, these findings indicate the vulnerability of the salience network in PD and its potential role in memory and executive dysfunction.</AbstractText>
<CopyrightInformation>© 2014 American Neurological Association.</CopyrightInformation>
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<Affiliation>Morton and Gloria Shulman Movement Disorder Unit and Edmond J. Safra Program in Parkinson Disease, Toronto Western Hospital, University Health Network, University of Toronto, Toronto, Ontario, Canada; Research Imaging Centre, Centre for Addiction and Mental Health, University of Toronto, Toronto, Ontario, Canada; Division of Brain, Imaging, and Behaviour-Systems Neuroscience, Toronto Western Research Institute, University Health Network, University of Toronto, Toronto, Ontario, Canada.</Affiliation>
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