La maladie de Parkinson en France (serveur d'exploration)

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Follow-up study of variants of the GIGYF2 gene in Chinese patients with Parkinson’s disease.

Identifieur interne : 001584 ( Main/Exploration ); précédent : 001583; suivant : 001585

Follow-up study of variants of the GIGYF2 gene in Chinese patients with Parkinson’s disease.

Auteurs : Lei Wang [République populaire de Chine] ; Ji-Feng Guo ; Wen-Wen Zhang ; Qian Xu ; Xing Zuo ; Chang-He Shi ; Lin-Zi Luo ; Jia Liu ; Liang Hu ; Ya-Cen Hu ; Xin-Xiang Yan ; Bei-Sha Tang

Source :

RBID : pubmed:22115759

Descripteurs français

English descriptors

Abstract

The Grb10-interacting GYF protein-2 gene (GIGYF2) is a PARK11 gene that reportedly has a causal role in familial Parkinson’s disease (PD) among populations from Italy and France. However, no comprehensive study of the GIGYF2 gene has been conducted among PD patients from mainland China. In our previous study, the GIGYF2 gene was directly sequenced, and nine missense variants and 14 polymorphisms were identified. For these 14 polymorphisms, in the present study we performed a case–control analysis for 300 PD patients and 200 healthy controls from mainland China. The c.297T>C p.Ala99Ala polymorphism was associated with increased risk with respect to the pathogenesis of sporadic PD. In conclusion, within the Chinese population, the c.297T>C p.Ala99Ala polymorphism of the GIGYF2 gene may be associated with an increased risk of developing PD.

DOI: 10.1016/j.jocn.2011.05.014
PubMed: 22115759


Affiliations:


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<div type="abstract" xml:lang="en">The Grb10-interacting GYF protein-2 gene (GIGYF2) is a PARK11 gene that reportedly has a causal role in familial Parkinson’s disease (PD) among populations from Italy and France. However, no comprehensive study of the GIGYF2 gene has been conducted among PD patients from mainland China. In our previous study, the GIGYF2 gene was directly sequenced, and nine missense variants and 14 polymorphisms were identified. For these 14 polymorphisms, in the present study we performed a case–control analysis for 300 PD patients and 200 healthy controls from mainland China. The c.297T>C p.Ala99Ala polymorphism was associated with increased risk with respect to the pathogenesis of sporadic PD. In conclusion, within the Chinese population, the c.297T>C p.Ala99Ala polymorphism of the GIGYF2 gene may be associated with an increased risk of developing PD.</div>
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