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

AbstractOBJECTIVE:
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.
METHODS:
We have used targeted high-throughput sequencing to characterize the 135kb SNCA locus in a large multinational cohort of patients with PD, PDD, and DLB and healthy controls.
RESULTS:
An analysis of 43 tagging single nucleotide polymorphisms across the SNCA locus shows 2 distinct association profiles for symptoms of parkinsonism and/or dementia, respectively, toward the 3' or the 5' of the SNCA gene. In addition, we define a specific haplotype in intron 4 that is directly associated with PDD. The PDD risk haplotype has been interrogated at single nucleotide resolution and is uniquely tagged by an expanded TTTCn repeat.
INTERPRETATION:
Our data show that PD, PDD, and DLB, rather than a disease continuum, have distinct genetic etiologies albeit within one genomic locus. Such results may serve as prognostic biomarkers to these disorders, to inform physicians and patients, and to assist in the design and stratification of clinical trials aimed at disease modification. Ann Neurol 2016;79:991-999.
AuthorsIlaria Guella, Daniel M Evans, Chelsea Szu-Tu, Ekaterina Nosova, Stephanie F Bortnick, SNCA Cognition Study Group, Jennifer G Goldman, John C Dalrymple-Alford, Gert J Geurtsen, Irene Litvan, Owen A Ross, Lefkos T Middleton, Laura Parkkinen, Matthew J Farrer
JournalAnnals of neurology (Ann Neurol) Vol. 79 Issue 6 Pg. 991-9 (Jun 2016) ISSN: 1531-8249 [Electronic] United States
PMID27091628 (Publication Type: Journal Article, Multicenter Study)
Copyright© 2016 American Neurological Association.
Chemical References
  • Biomarkers
  • alpha-Synuclein
Topics
  • Aged
  • Aged, 80 and over
  • Biomarkers
  • Case-Control Studies
  • Cognitive Dysfunction (complications, genetics)
  • Dementia (complications, genetics, psychology)
  • Female
  • Genetic Predisposition to Disease (genetics)
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Lewy Body Disease (complications, genetics, psychology)
  • Male
  • Parkinson Disease (complications, genetics, psychology)
  • Polymorphism, Single Nucleotide (genetics)
  • alpha-Synuclein (genetics)

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