4.7 Article

The MC1R Melanoma Risk Variant p.R160W Is Associated with Parkinson Disease

Journal

ANNALS OF NEUROLOGY
Volume 77, Issue 5, Pages 889-894

Publisher

WILEY
DOI: 10.1002/ana.24373

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Funding

  1. Fondo de Investigaciones Sanitarias [12/00840]
  2. Carlos III Health Institute
  3. Fondo Europeo de Desarrollo Regional of the European Commission
  4. Una manera de hacer Europa
  5. Catalan Government [AGAUR 2014 SGR 603]

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Epidemiological studies have reported the co-occurrence of Parkinson disease (PD) and melanoma. Common genetic variants in the MC1R (melanocortin 1 receptor) gene, which determines skin and hair color, are associated with melanoma. Here we investigated whether genetic variants in MC1R modulate the risk of PD by sequencing the entire gene in 870 PD patients and 736 controls ascertained from Spain. We found that the MC1R variant p.R160W (rs1805008) is marginally associated with PD (odds ratio=2.10, gender- and age-adjusted p=0.009, Bonferroni-corrected p=0.063). Our results suggest that MC1R genetic variants modulate the risk of PD disease in the Spanish population. Ann Neurol 2015;77:889-894

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