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

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α-synuclein genetic variability: A biomarker for dementia in Parkinson disease.

Identifieur interne : 000137 ( Main/Exploration ); précédent : 000136; suivant : 000138

α-synuclein genetic variability: A biomarker for dementia in Parkinson disease.

Auteurs : Ilaria Guella [Canada] ; Daniel M. Evans [Canada] ; Chelsea Szu-Tu [Canada] ; Ekaterina Nosova [Canada] ; Stephanie F. Bortnick [Canada] ; Jennifer G. Goldman [États-Unis] ; John C. Dalrymple-Alford [Nouvelle-Zélande] ; Gert J. Geurtsen [Pays-Bas] ; Irene Litvan [États-Unis] ; Owen A. Ross [États-Unis] ; Lefkos T. Middleton [Royaume-Uni] ; Laura Parkkinen [Royaume-Uni] ; Matthew J. Farrer [Canada]

Source :

RBID : pubmed:27091628

Abstract

The relationship between Parkinson disease (PD), PD with dementia (PDD), and dementia with Lewy bodies (DLB) has long been debated. Although PD is primarily considered a motor disorder, cognitive impairment is often present at diagnosis, and only ∼20% of patients remain cognitively intact in the long term. Alpha-synuclein (SNCA) was first implicated in the pathogenesis of the disease when point mutations and locus multiplications were identified in familial parkinsonism with dementia. In worldwide populations, SNCA genetic variability remains the most reproducible risk factor for idiopathic PD. However, few investigators have looked at SNCA variability in terms of cognitive outcomes.

DOI: 10.1002/ana.24664
PubMed: 27091628


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<div type="abstract" xml:lang="en">The relationship between Parkinson disease (PD), PD with dementia (PDD), and dementia with Lewy bodies (DLB) has long been debated. Although PD is primarily considered a motor disorder, cognitive impairment is often present at diagnosis, and only ∼20% of patients remain cognitively intact in the long term. Alpha-synuclein (SNCA) was first implicated in the pathogenesis of the disease when point mutations and locus multiplications were identified in familial parkinsonism with dementia. In worldwide populations, SNCA genetic variability remains the most reproducible risk factor for idiopathic PD. However, few investigators have looked at SNCA variability in terms of cognitive outcomes.</div>
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