Festination Correlates with SNCA Polymorphism in Chinese Patients with Parkinson’s Disease

The genetic basis of festination, a common motor symptom in Parkinson’s disease (PD), remains unclear. Since polymorphism in the alpha-synuclein (SNCA) gene is associated with PD phenotype, we examined whether such polymorphism is also associated with festination. SNCA polymorphisms rs11931074 and r...

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Veröffentlicht in:Parkinson's disease 2017-01, Vol.2017 (2017), p.1-4
Hauptverfasser: Xu, Yanming, Huang, Hongyan, Tian, Sijia, Zhao, Quanzhen, Yang, Xinglong, Zheng, Jinhua, Chen, Yalan
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Sprache:eng
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Zusammenfassung:The genetic basis of festination, a common motor symptom in Parkinson’s disease (PD), remains unclear. Since polymorphism in the alpha-synuclein (SNCA) gene is associated with PD phenotype, we examined whether such polymorphism is also associated with festination. SNCA polymorphisms rs11931074 and rs894278 were genotyped in a consecutive series of 258 patients with PD, of whom 122 (47.3%) suffered festination. Univariate analysis revealed significant differences in genotype and minor allele frequencies at rs11931074 or rs894278 between patients with festination and those without it (all p
ISSN:2090-8083
2042-0080
DOI:10.1155/2017/3176805