Movement Disorders (revue)

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The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study.

Identifieur interne : 000344 ( PubMed/Curation ); précédent : 000343; suivant : 000345

The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study.

Auteurs : Madeleine E. Sharp [États-Unis] ; Elise Caccappolo ; Helen Mejia-Santana ; Ming-X Tang ; Llency Rosado ; Martha Orbe Reilly ; Diana Ruiz ; Elan D. Louis ; Cynthia Comella ; Martha Nance ; Susan Bressman ; William K. Scott ; Caroline Tanner ; Cheryl Waters ; Stanley Fahn ; Lucien Cote ; Blair Ford ; Michael Rezak ; Kevin Novak ; Joseph H. Friedman ; Ronald Pfeiffer ; Haydeh Payami ; Eric Molho ; Stuart A. Factor ; John Nutt ; Carmen Serrano ; Maritza Arroyo ; Michael W. Pauciulo ; William C. Nichols ; Lorraine N. Clark ; Roy N. Alcalay ; Karen S. Marder

Source :

RBID : pubmed:25393808

English descriptors

Abstract

Few studies have systematically investigated the association between PARKIN genotype and psychiatric co-morbidities of Parkison's disease (PD). PARKIN-associated PD is characterized by severe nigral dopaminergic neuronal loss, a finding that may have implications for behaviors rooted in dopaminergic circuits such as obsessive-compulsive symptoms (OCS).

DOI: 10.1002/mds.26065
PubMed: 25393808

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pubmed:25393808

Le document en format XML

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<term>Adult</term>
<term>Age of Onset</term>
<term>Aged</term>
<term>Female</term>
<term>Genetic Predisposition to Disease</term>
<term>Genetic Testing</term>
<term>Genotype</term>
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<term>Male</term>
<term>Middle Aged</term>
<term>Mutation (genetics)</term>
<term>Obsessive-Compulsive Disorder (etiology)</term>
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<term>Obsessive-Compulsive Disorder</term>
<term>Parkinson Disease</term>
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<term>Adult</term>
<term>Age of Onset</term>
<term>Aged</term>
<term>Female</term>
<term>Genetic Predisposition to Disease</term>
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<front>
<div type="abstract" xml:lang="en">Few studies have systematically investigated the association between PARKIN genotype and psychiatric co-morbidities of Parkison's disease (PD). PARKIN-associated PD is characterized by severe nigral dopaminergic neuronal loss, a finding that may have implications for behaviors rooted in dopaminergic circuits such as obsessive-compulsive symptoms (OCS).</div>
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<Year>2015</Year>
<Month>02</Month>
<Day>04</Day>
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<DateCompleted>
<Year>2015</Year>
<Month>10</Month>
<Day>22</Day>
</DateCompleted>
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<Year>2015</Year>
<Month>07</Month>
<Day>10</Day>
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<ISSN IssnType="Electronic">1531-8257</ISSN>
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<Issue>2</Issue>
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<Year>2015</Year>
<Month>Feb</Month>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
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<ArticleTitle>The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study.</ArticleTitle>
<Pagination>
<MedlinePgn>278-83</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1002/mds.26065</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Few studies have systematically investigated the association between PARKIN genotype and psychiatric co-morbidities of Parkison's disease (PD). PARKIN-associated PD is characterized by severe nigral dopaminergic neuronal loss, a finding that may have implications for behaviors rooted in dopaminergic circuits such as obsessive-compulsive symptoms (OCS).</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">The Schedule of Compulsions and Obsessions Patient Inventory (SCOPI) was administered to 104 patients with early-onset PD and 257 asymptomatic first-degree relatives. Carriers of one and two PARKIN mutations were compared with noncarriers.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Among patients, carriers scored lower than noncarriers in adjusted models (one-mutation: 13.9 point difference, P = 0.03; two-mutation: 24.1, P = 0.001), where lower scores indicate less OCS. Among asymptomatic relatives, a trend toward the opposite was seen: mutation carriers scored higher than noncarriers (one mutation, P = 0.05; two mutations, P = 0.13).</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">First, a significant association was found between PARKIN mutation status and obsessive-compulsive symptom level in both PD and asymptomatic patients, suggesting that OCS might represent an early non-motor dopamine-dependent feature. Second, irrespective of disease status, heterozygotes were significantly different from noncarriers, suggesting that PARKIN heterozygosity may contribute to phenotype. © 2014 International Parkinson and Movement Disorder Society.</AbstractText>
<CopyrightInformation>© 2014 International Parkinson and Movement Disorder Society.</CopyrightInformation>
</Abstract>
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