Literature DB >> 20227461

Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China.

Qing-Zhou Fei1, Li Cao, Qin Xiao, Ting Zhang, Lan Zheng, Xi-Jin Wang, Gang Wang, Hai-Yan Zhou, Ying Wang, Sheng-Di Chen.   

Abstract

ATP13A2 (PARK9) mutations are related to Kufor-Rakeb syndrome (KRS). We performed genetic analysis of the Ala746Thr variant in an independent cohort of the patients with PD and healthy controls from mainland China. The Ala746Thr variant was present in 1/532 (0.19%) of PD compared with 1/480 (0.21%) of healthy controls (odds ratio=0.90, 95% CI 0.06, 14.39, P=1.00). The two subjects carried the heterozygous genotype. Subset analysis in the group </=50 years of age revealed a prevalence of 0.7% in PD compared with 0% in healthy controls and in the group >50 years of age showed 0% in PD versus 0.3% in healthy controls. We did not observe a significant association between Ala746Thr and Parkinson's disease in Han Chinese population, even after stratification by age at onset. The results suggested that Ala746Thr variant was not a major susceptible factor for PD in Han Chinese people. Copyright 2010 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20227461     DOI: 10.1016/j.neulet.2010.03.018

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  6 in total

1.  Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78).

Authors:  Alejandro Estrada-Cuzcano; Shaun Martin; Teodora Chamova; Matthis Synofzik; Dagmar Timmann; Tine Holemans; Albena Andreeva; Jennifer Reichbauer; Riet De Rycke; Dae-In Chang; Sarah van Veen; Jean Samuel; Ludger Schöls; Thorsten Pöppel; Danny Mollerup Sørensen; Bob Asselbergh; Christine Klein; Stephan Zuchner; Albena Jordanova; Peter Vangheluwe; Ivailo Tournev; Rebecca Schüle
Journal:  Brain       Date:  2017-02       Impact factor: 13.501

2.  Emerging links between pediatric lysosomal storage diseases and adult parkinsonism.

Authors:  Daniel Ysselstein; Joshua M Shulman; Dimitri Krainc
Journal:  Mov Disord       Date:  2019-02-06       Impact factor: 10.338

3.  The role of the Ala746Thr variant in the ATP13A2 gene among Chinese patients with Parkinson's disease.

Authors:  Anne Y Y Chan; Larry Baum; Nelson L S Tang; Christine Y K Lau; Ping Wing Ng; Kwok Fai Hui; Yoshi Mizuno; Justin Y Kwan; Vincent C T Mok; Sheng-Han Kuo
Journal:  J Clin Neurosci       Date:  2013-03-20       Impact factor: 1.961

4.  ATP13A2 Gene Variants in Patients with Parkinson's Disease in Xinjiang.

Authors:  Dan Wang; Hua Gao; Yanxia Li; Sen Jiang; Xinling Yang
Journal:  Biomed Res Int       Date:  2020-11-30       Impact factor: 3.411

Review 5.  Mutations in the ATP13A2 gene and Parkinsonism: a preliminary review.

Authors:  Xinglong Yang; Yanming Xu
Journal:  Biomed Res Int       Date:  2014-08-14       Impact factor: 3.411

Review 6.  The Emerging Role of the Lysosome in Parkinson's Disease.

Authors:  Alba Navarro-Romero; Marta Montpeyó; Marta Martinez-Vicente
Journal:  Cells       Date:  2020-11-02       Impact factor: 6.600

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.