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

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TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease.

Identifieur interne : 000841 ( PubMed/Checkpoint ); précédent : 000840; suivant : 000842

TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease.

Auteurs : Sruti Rayaprolu [États-Unis] ; Bianca Mullen ; Matt Baker ; Timothy Lynch ; Elizabeth Finger ; William W. Seeley ; Kimmo J. Hatanpaa ; Catherine Lomen-Hoerth ; Andrew Kertesz ; Eileen H. Bigio ; Carol Lippa ; Keith A. Josephs ; David S. Knopman ; Charles L. White ; Richard Caselli ; Ian R. Mackenzie ; Bruce L. Miller ; Magdalena Boczarska-Jedynak ; Grzegorz Opala ; Anna Krygowska-Wajs ; Maria Barcikowska ; Steven G. Younkin ; Ronald C. Petersen ; Nilüfer Ertekin-Taner ; Ryan J. Uitti ; James F. Meschia ; Kevin B. Boylan ; Bradley F. Boeve ; Neill R. Graff-Radford ; Zbigniew K. Wszolek ; Dennis W. Dickson ; Rosa Rademakers ; Owen A. Ross

Source :

RBID : pubmed:23800361

English descriptors

Abstract

A rare variant in the Triggering Receptor Expressed on Myeloid cells 2 (TREM2) gene has been reported to be a genetic risk factor for Alzheimer's disease by two independent groups (Odds ratio between 2.9-4.5). Given the key role of TREM2 in the effective phagocytosis of apoptotic neuronal cells by microglia, we hypothesized that dysfunction of TREM2 may play a more generalized role in neurodegeneration. With this in mind we set out to assess the genetic association of the Alzheimer's disease-related risk variant in TREM2 (rs75932628, p.R47H) with other related neurodegenerative disorders.

DOI: 10.1186/1750-1326-8-19
PubMed: 23800361


Affiliations:


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pubmed:23800361

Le document en format XML

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<div type="abstract" xml:lang="en">A rare variant in the Triggering Receptor Expressed on Myeloid cells 2 (TREM2) gene has been reported to be a genetic risk factor for Alzheimer's disease by two independent groups (Odds ratio between 2.9-4.5). Given the key role of TREM2 in the effective phagocytosis of apoptotic neuronal cells by microglia, we hypothesized that dysfunction of TREM2 may play a more generalized role in neurodegeneration. With this in mind we set out to assess the genetic association of the Alzheimer's disease-related risk variant in TREM2 (rs75932628, p.R47H) with other related neurodegenerative disorders.</div>
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<Month>06</Month>
<Day>26</Day>
</DateCreated>
<DateCompleted>
<Year>2013</Year>
<Month>09</Month>
<Day>20</Day>
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<Month>10</Month>
<Day>19</Day>
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<Volume>8</Volume>
<PubDate>
<Year>2013</Year>
<Month>Jun</Month>
<Day>21</Day>
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<Title>Molecular neurodegeneration</Title>
<ISOAbbreviation>Mol Neurodegener</ISOAbbreviation>
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<ArticleTitle>TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease.</ArticleTitle>
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<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">A rare variant in the Triggering Receptor Expressed on Myeloid cells 2 (TREM2) gene has been reported to be a genetic risk factor for Alzheimer's disease by two independent groups (Odds ratio between 2.9-4.5). Given the key role of TREM2 in the effective phagocytosis of apoptotic neuronal cells by microglia, we hypothesized that dysfunction of TREM2 may play a more generalized role in neurodegeneration. With this in mind we set out to assess the genetic association of the Alzheimer's disease-related risk variant in TREM2 (rs75932628, p.R47H) with other related neurodegenerative disorders.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The study included 609 patients with frontotemporal dementia, 765 with amyotrophic lateral sclerosis, 1493 with Parkinson's disease, 772 with progressive supranuclear palsy, 448 with ischemic stroke and 1957 controls subjects free of neurodegenerative disease. A significant association was observed for the TREM2 p.R47H substitution in susceptibility to frontotemporal dementia (OR = 5.06; p-value = 0.001) and Parkinson's disease (OR = 2.67; p-value = 0.026), while no evidence of association with risk of amyotrophic lateral sclerosis, progressive supranuclear palsy or ischemic stroke was observed.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Our results suggest that the TREM2 p.R47H substitution is a risk factor for frontotemporal dementia and Parkinson's disease in addition to Alzheimer's disease. These findings suggest a more general role for TREM2 dysfunction in neurodegeneration, which could be related to its role in the immune response.</AbstractText>
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