Impaired corticostriatal connectivity in impulse control disorders in Parkinson disease.
Identifieur interne : 001696 ( Ncbi/Merge ); précédent : 001695; suivant : 001697Impaired corticostriatal connectivity in impulse control disorders in Parkinson disease.
Auteurs : Nicolas Carriere [France] ; Renaud Lopes [France] ; Luc Defebvre [France] ; Christine Delmaire [France] ; Kathy Dujardin [France]Source :
- Neurology [ 1526-632X ] ; 2015.
English descriptors
- KwdEn :
- Aged, Atrophy (pathology), Brain Mapping (methods), Cerebral Cortex (pathology), Cerebral Cortex (physiopathology), Disruptive, Impulse Control, and Conduct Disorders (etiology), Disruptive, Impulse Control, and Conduct Disorders (physiopathology), Humans, Magnetic Resonance Imaging, Male, Middle Aged, Neostriatum (physiopathology), Parkinson Disease (complications), Parkinson Disease (physiopathology).
- MESH :
- complications : Parkinson Disease.
- etiology : Disruptive, Impulse Control, and Conduct Disorders.
- methods : Brain Mapping.
- pathology : Atrophy, Cerebral Cortex.
- physiopathology : Cerebral Cortex, Disruptive, Impulse Control, and Conduct Disorders, Neostriatum, Parkinson Disease.
- Aged, Humans, Magnetic Resonance Imaging, Male, Middle Aged.
Abstract
To compare the striatum's resting-state functional connectivity in patients with Parkinson disease (PD) with and without impulse control disorders (ICDs).
DOI: 10.1212/WNL.0000000000001619
PubMed: 25925985
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 000349
- to stream PubMed, to step Curation: 000347
- to stream PubMed, to step Checkpoint: 000347
Links to Exploration step
pubmed:25925985Le document en format XML
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<term>Atrophy (pathology)</term>
<term>Brain Mapping (methods)</term>
<term>Cerebral Cortex (pathology)</term>
<term>Cerebral Cortex (physiopathology)</term>
<term>Disruptive, Impulse Control, and Conduct Disorders (etiology)</term>
<term>Disruptive, Impulse Control, and Conduct Disorders (physiopathology)</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Neostriatum (physiopathology)</term>
<term>Parkinson Disease (complications)</term>
<term>Parkinson Disease (physiopathology)</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Atrophy</term>
<term>Cerebral Cortex</term>
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<term>Disruptive, Impulse Control, and Conduct Disorders</term>
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<term>Parkinson Disease</term>
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<term>Humans</term>
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<front><div type="abstract" xml:lang="en">To compare the striatum's resting-state functional connectivity in patients with Parkinson disease (PD) with and without impulse control disorders (ICDs).</div>
</front>
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<Month>05</Month>
<Day>26</Day>
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<Day>03</Day>
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<Day>19</Day>
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<Issue>21</Issue>
<PubDate><Year>2015</Year>
<Month>May</Month>
<Day>26</Day>
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<Title>Neurology</Title>
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<ArticleTitle>Impaired corticostriatal connectivity in impulse control disorders in Parkinson disease.</ArticleTitle>
<Pagination><MedlinePgn>2116-23</MedlinePgn>
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<Abstract><AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">To compare the striatum's resting-state functional connectivity in patients with Parkinson disease (PD) with and without impulse control disorders (ICDs).</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Twenty patients with PD and ICDs, 19 patients with PD but no ICDs, and 19 healthy controls underwent fMRI in the resting state. The ventral striatum, dorsal caudate, and anterior and posterior putamen were segmented semiautomatically. For each region of interest, a seed-based connectivity analysis was performed on preprocessed fMRI data mapped on the ipsilateral cortical surface. An additional cortical thickness analysis was used to assess and compare gray matter atrophy in the 3 study subgroups.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The presence of an ICD in patients with PD was associated with functional disconnection between the left anterior putamen and both the left inferior temporal gyrus and the left anterior cingulate gyrus, as well as a trend toward a functional disconnection between several motor and associative striatal regions and limbic, associative, and motor cortical regions. Patients without ICDs did not differ from healthy controls in corticostriatal connectivity. The cortical thickness analysis did not reveal any significant differences among the 3 study subgroups.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">In PD, ICDs are associated with altered connectivity between an associative striatal area (the left anterior putamen) and associative and limbic cortical regions (the left inferior temporal gyrus and the left anterior cingulate gyrus).</AbstractText>
<CopyrightInformation>© 2015 American Academy of Neurology.</CopyrightInformation>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Carriere</LastName>
<ForeName>Nicolas</ForeName>
<Initials>N</Initials>
<AffiliationInfo><Affiliation>From the Université Lille Nord de France (N.C., R.L., L.D., C.D., K.D.), U1171, Lille; Service de Neurologie et Pathologie du Mouvement (N.C., L.D., K.D.) and Service de Neuroradiologie (R.L., C.D.), Centre Hospitalier Régional Universitaire, Lille, France. nicolas.carriere@chru-lille.fr.</Affiliation>
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<ForeName>Renaud</ForeName>
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<AffiliationInfo><Affiliation>From the Université Lille Nord de France (N.C., R.L., L.D., C.D., K.D.), U1171, Lille; Service de Neurologie et Pathologie du Mouvement (N.C., L.D., K.D.) and Service de Neuroradiologie (R.L., C.D.), Centre Hospitalier Régional Universitaire, Lille, France.</Affiliation>
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<Author ValidYN="Y"><LastName>Dujardin</LastName>
<ForeName>Kathy</ForeName>
<Initials>K</Initials>
<AffiliationInfo><Affiliation>From the Université Lille Nord de France (N.C., R.L., L.D., C.D., K.D.), U1171, Lille; Service de Neurologie et Pathologie du Mouvement (N.C., L.D., K.D.) and Service de Neuroradiologie (R.L., C.D.), Centre Hospitalier Régional Universitaire, Lille, France.</Affiliation>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName>
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<MeshHeading><DescriptorName UI="D001284" MajorTopicYN="N">Atrophy</DescriptorName>
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<QualifierName UI="Q000503" MajorTopicYN="Y">physiopathology</QualifierName>
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<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
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<affiliations><list><country><li>France</li>
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<region><li>Hauts-de-France</li>
<li>Nord-Pas-de-Calais</li>
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<settlement><li>Lille</li>
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<orgName><li>Université Lille 2</li>
<li>Université Lille Nord de France</li>
</orgName>
</list>
<tree><country name="France"><region name="Hauts-de-France"><name sortKey="Carriere, Nicolas" sort="Carriere, Nicolas" uniqKey="Carriere N" first="Nicolas" last="Carriere">Nicolas Carriere</name>
</region>
<name sortKey="Defebvre, Luc" sort="Defebvre, Luc" uniqKey="Defebvre L" first="Luc" last="Defebvre">Luc Defebvre</name>
<name sortKey="Delmaire, Christine" sort="Delmaire, Christine" uniqKey="Delmaire C" first="Christine" last="Delmaire">Christine Delmaire</name>
<name sortKey="Dujardin, Kathy" sort="Dujardin, Kathy" uniqKey="Dujardin K" first="Kathy" last="Dujardin">Kathy Dujardin</name>
<name sortKey="Lopes, Renaud" sort="Lopes, Renaud" uniqKey="Lopes R" first="Renaud" last="Lopes">Renaud Lopes</name>
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