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

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Inflammatory profile discriminates clinical subtypes in LRRK2-associated Parkinson's disease.

Identifieur interne : 000064 ( PubMed/Curation ); précédent : 000063; suivant : 000065

Inflammatory profile discriminates clinical subtypes in LRRK2-associated Parkinson's disease.

Auteurs : K. Brockmann [Allemagne] ; C. Schulte [Allemagne] ; N. Schneiderhan-Marra [Allemagne] ; A. Apel [Allemagne] ; C. Pont-Sunyer [Espagne] ; D. Vilas [Espagne] ; J. Ruiz-Martinez [Espagne] ; M. Langkamp [Allemagne] ; J-C Corvol [France] ; F. Cormier [France] ; T. Knorpp [Allemagne] ; T O Joos [Allemagne] ; A. Bernard [Allemagne] ; T. Gasser [Allemagne] ; C. Marras [Canada] ; B. Schüle [États-Unis] ; J O Aasly [Norvège] ; T. Foroud [États-Unis] ; J F Marti-Masso [Espagne] ; A. Brice [France] ; E. Tolosa [Espagne] ; D. Berg [Allemagne] ; W. Maetzler [Allemagne]

Source :

RBID : pubmed:28102045

Abstract

The presentation of Parkinson's disease patients with mutations in the LRRK2 gene (PDLRRK2 ) is highly variable, suggesting a strong influence of modifying factors. In this context, inflammation is a potential candidate inducing clinical subtypes.

DOI: 10.1111/ene.13223
PubMed: 28102045

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pubmed:28102045

Le document en format XML

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<wicri:regionArea>Department of Neurology, St Olavs Hospital, Trondheim</wicri:regionArea>
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<name sortKey="Foroud, T" sort="Foroud, T" uniqKey="Foroud T" first="T" last="Foroud">T. Foroud</name>
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<nlm:affiliation>Department of Medical and Molecular Genetics, Indiana University, Bloomington, IN, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Medical and Molecular Genetics, Indiana University, Bloomington, IN</wicri:regionArea>
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<author>
<name sortKey="Marti Masso, J F" sort="Marti Masso, J F" uniqKey="Marti Masso J" first="J F" last="Marti-Masso">J F Marti-Masso</name>
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<country xml:lang="fr">Espagne</country>
<wicri:regionArea>Hospital Universitario Donostia, Biodonostia Institut, San Sebastián, Guipuzcoa</wicri:regionArea>
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<name sortKey="Brice, A" sort="Brice, A" uniqKey="Brice A" first="A" last="Brice">A. Brice</name>
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<nlm:affiliation>Département de Génétique et Cytogénétique, Hôpital de la Pitié Salpêtrière, Sorbonne Universités, INSERM, Paris, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
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<name sortKey="Tolosa, E" sort="Tolosa, E" uniqKey="Tolosa E" first="E" last="Tolosa">E. Tolosa</name>
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<nlm:affiliation>Parkinson's Disease and Movement Disorders Unit, Neurology Service, Hospital Clinic de Barcelona, Universitat de Barcelona, Institut d'Investigacions Biomediques August Pi I Sunyer (IDIBAPS), Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Barcelona, Spain.</nlm:affiliation>
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<name sortKey="Berg, D" sort="Berg, D" uniqKey="Berg D" first="D" last="Berg">D. Berg</name>
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<nlm:affiliation>Department of Neurodegenerative Diseases and Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.</nlm:affiliation>
<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Neurodegenerative Diseases and Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen</wicri:regionArea>
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<name sortKey="Maetzler, W" sort="Maetzler, W" uniqKey="Maetzler W" first="W" last="Maetzler">W. Maetzler</name>
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<nlm:affiliation>Department of Neurodegenerative Diseases and Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.</nlm:affiliation>
<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Neurodegenerative Diseases and Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen</wicri:regionArea>
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<series>
<title level="j">European journal of neurology</title>
<idno type="eISSN">1468-1331</idno>
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<div type="abstract" xml:lang="en">The presentation of Parkinson's disease patients with mutations in the LRRK2 gene (PDLRRK2 ) is highly variable, suggesting a strong influence of modifying factors. In this context, inflammation is a potential candidate inducing clinical subtypes.</div>
</front>
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<DateCreated>
<Year>2017</Year>
<Month>01</Month>
<Day>19</Day>
</DateCreated>
<DateRevised>
<Year>2017</Year>
<Month>01</Month>
<Day>19</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1468-1331</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>24</Volume>
<Issue>2</Issue>
<PubDate>
<Year>2017</Year>
<Month>Feb</Month>
</PubDate>
</JournalIssue>
<Title>European journal of neurology</Title>
<ISOAbbreviation>Eur. J. Neurol.</ISOAbbreviation>
</Journal>
<ArticleTitle>Inflammatory profile discriminates clinical subtypes in LRRK2-associated Parkinson's disease.</ArticleTitle>
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<MedlinePgn>427-e6</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/ene.13223</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND AND PURPOSE" NlmCategory="OBJECTIVE">The presentation of Parkinson's disease patients with mutations in the LRRK2 gene (PDLRRK2 ) is highly variable, suggesting a strong influence of modifying factors. In this context, inflammation is a potential candidate inducing clinical subtypes.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">An extensive battery of peripheral inflammatory markers was measured in human serum in a multicentre cohort of 142 PDLRRK2 patients from the MJFF LRRK2 Consortium, stratified by three different subtypes as recently proposed for idiopathic Parkinson's disease: diffuse/malignant, intermediate and mainly pure motor.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Patients classified as diffuse/malignant presented with the highest levels of the pro-inflammatory proteins interleukin 8 (IL-8), monocyte chemotactic protein 1 (MCP-1) and macrophage inflammatory protein 1-β (MIP-1-β) paralleled by high levels of the neurotrophic protein brain-derived neurotrophic factor (BDNF). It was also possible to distinguish the clinical subtypes based on their inflammatory profile by using discriminant and area under the receiver operating characteristic curve analysis.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Inflammation seems to be associated with the presence of a specific clinical subtype in PDLRRK2 that is characterized by a broad and more severely affected spectrum of motor and non-motor symptoms. The pro-inflammatory metabolites IL-8, MCP-1 and MIP-1-β as well as BDNF are interesting candidates to be included in biomarker panels that aim to differentiate subtypes in PDLRRK2 and predict progression.</AbstractText>
<CopyrightInformation>© 2017 EAN.</CopyrightInformation>
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<Author ValidYN="Y">
<LastName>Brockmann</LastName>
<ForeName>K</ForeName>
<Initials>K</Initials>
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<Affiliation>Department of Neurodegenerative Diseases and Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.</Affiliation>
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<LastName>Schulte</LastName>
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<Initials>C</Initials>
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<Affiliation>Department of Neurodegenerative Diseases and Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.</Affiliation>
</AffiliationInfo>
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<ForeName>N</ForeName>
<Initials>N</Initials>
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</AffiliationInfo>
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<Affiliation>Department of Neurodegenerative Diseases and Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.</Affiliation>
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<LastName>Pont-Sunyer</LastName>
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</AffiliationInfo>
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</AffiliationInfo>
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<Author ValidYN="Y">
<LastName>Gasser</LastName>
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<Affiliation>Department of Neurodegenerative Diseases and Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.</Affiliation>
</AffiliationInfo>
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<Affiliation>German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.</Affiliation>
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<AffiliationInfo>
<Affiliation>German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.</Affiliation>
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