Alpha-synuclein repeat variants and survival in Parkinson's disease.
Identifieur interne : 000570 ( PubMed/Corpus ); précédent : 000569; suivant : 000571Alpha-synuclein repeat variants and survival in Parkinson's disease.
Auteurs : Sun Ju Chung ; Joanna M. Biernacka ; Sebastian M. Armasu ; Kari Anderson ; Roberta Frigerio ; Jan O. Aasly ; Grazia Annesi ; Anna Rita Bentivoglio ; Laura Brighina ; Marie-Christine Chartier-Harlin ; Stefano Goldwurm ; Georgios Hadjigeorgiou ; Barbara Jasinska-Myga ; Beom Seok Jeon ; Yun Joong Kim ; Rejko Krüger ; Suzanne Lesage ; Katerina Markopoulou ; George Mellick ; Karen E. Morrison ; Andreas Puschmann ; Eng-King Tan ; David Crosiers ; Jessie Theuns ; Christine Van Broeckhoven ; Karin Wirdefeldt ; Zbigniew K. Wszolek ; Alexis Elbaz ; Demetrius M. MaraganoreSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2014.
English descriptors
- KwdEn :
- Adult, Age of Onset, Aged, Aged, 80 and over, Dinucleotide Repeats (genetics), Female, Gene Frequency, Genetic Association Studies, Genetic Predisposition to Disease (genetics), Genotype, Humans, International Cooperation, Male, Middle Aged, Parkinson Disease (genetics), Parkinson Disease (mortality), Survival, alpha-Synuclein (genetics).
- MESH :
- chemical , genetics : alpha-Synuclein.
- genetics : Dinucleotide Repeats, Genetic Predisposition to Disease, Parkinson Disease.
- mortality : Parkinson Disease.
- Adult, Age of Onset, Aged, Aged, 80 and over, Female, Gene Frequency, Genetic Association Studies, Genotype, Humans, International Cooperation, Male, Middle Aged, Survival.
Abstract
To determine whether α-synuclein dinucleotide repeat (REP1) genotypes are associated with survival in Parkinson's disease (PD).
DOI: 10.1002/mds.25841
PubMed: 24578302
Links to Exploration step
pubmed:24578302Le document en format XML
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<author><name sortKey="Chartier Harlin, Marie Christine" sort="Chartier Harlin, Marie Christine" uniqKey="Chartier Harlin M" first="Marie-Christine" last="Chartier-Harlin">Marie-Christine Chartier-Harlin</name>
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<author><name sortKey="Hadjigeorgiou, Georgios" sort="Hadjigeorgiou, Georgios" uniqKey="Hadjigeorgiou G" first="Georgios" last="Hadjigeorgiou">Georgios Hadjigeorgiou</name>
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<author><name sortKey="Jeon, Beom Seok" sort="Jeon, Beom Seok" uniqKey="Jeon B" first="Beom Seok" last="Jeon">Beom Seok Jeon</name>
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<author><name sortKey="Markopoulou, Katerina" sort="Markopoulou, Katerina" uniqKey="Markopoulou K" first="Katerina" last="Markopoulou">Katerina Markopoulou</name>
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<author><name sortKey="Mellick, George" sort="Mellick, George" uniqKey="Mellick G" first="George" last="Mellick">George Mellick</name>
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<author><name sortKey="Morrison, Karen E" sort="Morrison, Karen E" uniqKey="Morrison K" first="Karen E" last="Morrison">Karen E. Morrison</name>
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<author><name sortKey="Tan, Eng King" sort="Tan, Eng King" uniqKey="Tan E" first="Eng-King" last="Tan">Eng-King Tan</name>
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<author><name sortKey="Van Broeckhoven, Christine" sort="Van Broeckhoven, Christine" uniqKey="Van Broeckhoven C" first="Christine" last="Van Broeckhoven">Christine Van Broeckhoven</name>
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<author><name sortKey="Wszolek, Zbigniew K" sort="Wszolek, Zbigniew K" uniqKey="Wszolek Z" first="Zbigniew K" last="Wszolek">Zbigniew K. Wszolek</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="eISSN">1531-8257</idno>
<imprint><date when="2014" type="published">2014</date>
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<term>Age of Onset</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Dinucleotide Repeats (genetics)</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Genetic Association Studies</term>
<term>Genetic Predisposition to Disease (genetics)</term>
<term>Genotype</term>
<term>Humans</term>
<term>International Cooperation</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Parkinson Disease (genetics)</term>
<term>Parkinson Disease (mortality)</term>
<term>Survival</term>
<term>alpha-Synuclein (genetics)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>alpha-Synuclein</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Dinucleotide Repeats</term>
<term>Genetic Predisposition to Disease</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="mortality" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Age of Onset</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Genetic Association Studies</term>
<term>Genotype</term>
<term>Humans</term>
<term>International Cooperation</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Survival</term>
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<front><div type="abstract" xml:lang="en">To determine whether α-synuclein dinucleotide repeat (REP1) genotypes are associated with survival in Parkinson's disease (PD).</div>
</front>
</TEI>
<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">24578302</PMID>
<DateCreated><Year>2014</Year>
<Month>07</Month>
<Day>21</Day>
</DateCreated>
<DateCompleted><Year>2015</Year>
<Month>03</Month>
<Day>30</Day>
</DateCompleted>
<DateRevised><Year>2015</Year>
<Month>07</Month>
<Day>01</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1531-8257</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>29</Volume>
<Issue>8</Issue>
<PubDate><Year>2014</Year>
<Month>Jul</Month>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Alpha-synuclein repeat variants and survival in Parkinson's disease.</ArticleTitle>
<Pagination><MedlinePgn>1053-7</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1002/mds.25841</ELocationID>
<Abstract><AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">To determine whether α-synuclein dinucleotide repeat (REP1) genotypes are associated with survival in Parkinson's disease (PD).</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Investigators from the Genetic Epidemiology of Parkinson's Disease Consortium provided REP1 genotypes and baseline and follow-up clinical data for cases. The primary outcome was time to death. Cox proportional hazards regression models were used to assess the association of REP1 genotypes with survival.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Twenty-one sites contributed data for 6,154 cases. There was no significant association between α-synuclein REP1 genotypes and survival in PD. However, there was a significant association between REP1 genotypes and age at onset of PD (hazard ratio: 1.06; 95% confidence interval: 1.01-1.10; P value = 0.01).</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">In our large consortium study, α-synuclein REP1 genotypes were not associated with survival in PD. Further studies of α-synuclein's role in disease progression and long-term outcomes are needed.</AbstractText>
<CopyrightInformation>© 2014 International Parkinson and Movement Disorder Society.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Chung</LastName>
<ForeName>Sun Ju</ForeName>
<Initials>SJ</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Biernacka</LastName>
<ForeName>Joanna M</ForeName>
<Initials>JM</Initials>
</Author>
<Author ValidYN="Y"><LastName>Armasu</LastName>
<ForeName>Sebastian M</ForeName>
<Initials>SM</Initials>
</Author>
<Author ValidYN="Y"><LastName>Anderson</LastName>
<ForeName>Kari</ForeName>
<Initials>K</Initials>
</Author>
<Author ValidYN="Y"><LastName>Frigerio</LastName>
<ForeName>Roberta</ForeName>
<Initials>R</Initials>
</Author>
<Author ValidYN="Y"><LastName>Aasly</LastName>
<ForeName>Jan O</ForeName>
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</Author>
<Author ValidYN="Y"><LastName>Annesi</LastName>
<ForeName>Grazia</ForeName>
<Initials>G</Initials>
</Author>
<Author ValidYN="Y"><LastName>Bentivoglio</LastName>
<ForeName>Anna Rita</ForeName>
<Initials>AR</Initials>
</Author>
<Author ValidYN="Y"><LastName>Brighina</LastName>
<ForeName>Laura</ForeName>
<Initials>L</Initials>
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<Author ValidYN="Y"><LastName>Chartier-Harlin</LastName>
<ForeName>Marie-Christine</ForeName>
<Initials>MC</Initials>
</Author>
<Author ValidYN="Y"><LastName>Goldwurm</LastName>
<ForeName>Stefano</ForeName>
<Initials>S</Initials>
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<Author ValidYN="Y"><LastName>Hadjigeorgiou</LastName>
<ForeName>Georgios</ForeName>
<Initials>G</Initials>
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<Author ValidYN="Y"><LastName>Jeon</LastName>
<ForeName>Beom Seok</ForeName>
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<ForeName>Yun Joong</ForeName>
<Initials>YJ</Initials>
</Author>
<Author ValidYN="Y"><LastName>Krüger</LastName>
<ForeName>Rejko</ForeName>
<Initials>R</Initials>
</Author>
<Author ValidYN="Y"><LastName>Lesage</LastName>
<ForeName>Suzanne</ForeName>
<Initials>S</Initials>
</Author>
<Author ValidYN="Y"><LastName>Markopoulou</LastName>
<ForeName>Katerina</ForeName>
<Initials>K</Initials>
</Author>
<Author ValidYN="Y"><LastName>Mellick</LastName>
<ForeName>George</ForeName>
<Initials>G</Initials>
</Author>
<Author ValidYN="Y"><LastName>Morrison</LastName>
<ForeName>Karen E</ForeName>
<Initials>KE</Initials>
</Author>
<Author ValidYN="Y"><LastName>Puschmann</LastName>
<ForeName>Andreas</ForeName>
<Initials>A</Initials>
</Author>
<Author ValidYN="Y"><LastName>Tan</LastName>
<ForeName>Eng-King</ForeName>
<Initials>EK</Initials>
</Author>
<Author ValidYN="Y"><LastName>Crosiers</LastName>
<ForeName>David</ForeName>
<Initials>D</Initials>
</Author>
<Author ValidYN="Y"><LastName>Theuns</LastName>
<ForeName>Jessie</ForeName>
<Initials>J</Initials>
</Author>
<Author ValidYN="Y"><LastName>Van Broeckhoven</LastName>
<ForeName>Christine</ForeName>
<Initials>C</Initials>
</Author>
<Author ValidYN="Y"><LastName>Wirdefeldt</LastName>
<ForeName>Karin</ForeName>
<Initials>K</Initials>
</Author>
<Author ValidYN="Y"><LastName>Wszolek</LastName>
<ForeName>Zbigniew K</ForeName>
<Initials>ZK</Initials>
</Author>
<Author ValidYN="Y"><LastName>Elbaz</LastName>
<ForeName>Alexis</ForeName>
<Initials>A</Initials>
</Author>
<Author ValidYN="Y"><LastName>Maraganore</LastName>
<ForeName>Demetrius M</ForeName>
<Initials>DM</Initials>
</Author>
<Author ValidYN="Y"><CollectiveName>Genetic Epidemiology of Parkinson's Disease Consortium</CollectiveName>
</Author>
</AuthorList>
<Language>eng</Language>
<GrantList CompleteYN="Y"><Grant><GrantID>P50 NS072187</GrantID>
<Acronym>NS</Acronym>
<Agency>NINDS NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant><GrantID>P50 NS072187</GrantID>
<Acronym>NS</Acronym>
<Agency>NINDS NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant><GrantID>R01 ES010751</GrantID>
<Acronym>ES</Acronym>
<Agency>NIEHS NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant><Agency>Medical Research Council</Agency>
<Country>United Kingdom</Country>
</Grant>
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<ArticleDate DateType="Electronic"><Year>2014</Year>
<Month>02</Month>
<Day>27</Day>
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<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Mov Disord</MedlineTA>
<NlmUniqueID>8610688</NlmUniqueID>
<ISSNLinking>0885-3185</ISSNLinking>
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<NameOfSubstance UI="D051844">alpha-Synuclein</NameOfSubstance>
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</ChemicalList>
<CitationSubset>IM</CitationSubset>
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