4.6 Article

Alpha-Synuclein Repeat Variants and Survival in Parkinson's Disease

Journal

MOVEMENT DISORDERS
Volume 29, Issue 8, Pages 1053-1057

Publisher

WILEY
DOI: 10.1002/mds.25841

Keywords

Parkinson's disease; alpha-synuclein; gene; survival; association

Funding

  1. Italian Telethon Foundation [GTB07001]
  2. Fondazione Grigioni per il Morbo di Parkinson
  3. National Institutes of Health [R01 ES10751, P50 NS072187]
  4. Medical Research Council UK
  5. Midlands Neuroscience Teaching and Research Fund
  6. Queen Elizabeth Hospital Birmingham Charity
  7. Interuniversity Attraction Poles program of the Belgian Science Policy Office
  8. Foundation for Alzheimer Research
  9. Belgian Parkinson Foundation
  10. Methusalem Excellence Program of the Flemish Government
  11. Research Foundation Flanders
  12. Agency for Innovation by Science and Technology Flanders
  13. Special Research Fund of the University of Antwerp, Antwerp, Belgium
  14. Mayo Clinic Florida Research Committee CR program

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Objectives: To determine whether alpha-synuclein dinucleotide repeat (REP1) genotypes are associated with survival in Parkinson's disease (PD). 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. Results: Twenty-one sites contributed data for 6,154 cases. There was no significant association between alpha-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). Conclusions: In our large consortium study, alpha-synuclein REP1 genotypes were not associated with survival in PD. Further studies of alpha-synuclein's role in disease progression and long-term outcomes are needed. (C) 2014 International Parkinson and Movement Disorder Society

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