Meta-analysis of association between PITX3 gene polymorphism and Parkinson's disease

被引:11
|
作者
Tang, Lanhua [1 ,2 ,3 ]
Zhao, Shushan [1 ,4 ]
Wang, Meiping [2 ]
Sheth, Aniruddha [5 ]
Zhao, Zijin [1 ]
Chen, Luyao [1 ]
Fan, Xuegong [6 ]
Chen, Lizhang [7 ]
机构
[1] Cent S Univ, Xiangya Hosp, Eight Year Program, Changsha 410008, Hunan, Peoples R China
[2] Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China
[3] Cent S Univ, Xiangya Hosp, Dept Oncol, Changsha 410008, Hunan, Peoples R China
[4] Cent S Univ, Xiangya Hosp, Dept Spine Surg, Changsha 410008, Hunan, Peoples R China
[5] Univ Tasmania, Sch Med, Hobart, Tas, Australia
[6] Cent S Univ, Xiangya Hosp, Dept Infect Dis, Changsha 410008, Hunan, Peoples R China
[7] Cent S Univ, Sch Publ Hlth, Changsha 410008, Hunan, Peoples R China
关键词
PITX3; gene; Parkinson's disease; Meta-analysis; Gene polymorphism; MESENCEPHALIC DOPAMINERGIC-NEURONS; TRANSCRIPTION FACTOR PITX3; CHINESE POPULATION; SUBSTANTIA-NIGRA; RESPONSE ELEMENT; RETINOIC ACID; IN-VITRO; EXPRESSION; DIAGNOSIS; PROMOTER;
D O I
10.1016/j.jns.2012.02.025
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Parkinson's disease (PD) is one of the most common neurodegenerative diseases. Several studies had researched the association between the PITX3 gene polymorphism and Parkinson's disease. However, the results were inconsistent. To evaluate whether PITX3 gene polymorphism is involved in the risk of PD we conducted this metaanalysis. All the eligible studies were searched from the databases of Cochrane Central Register of Controlled Trials (CENTRAL) in The Cochrane Library, MEDLINE, EMBASE, and Science Citation Index EXPANDED in any languages up to May 2011. Finally ten studies about PITX3 gene including 5172 patients and 7290 controls were identified for meta-analysis. Meta-analysis was carried out to evaluate whether PITX3 gene polymorphism was associated with PD, and subgroup analysis was also performed when necessary. This meta-analysis finds that rs4919621 allele A was significantly associated with PD in the Caucasian population (P=0.04,). Subgroup analysis of early onset PD (EOPD) and late onset PD (LOPD) revealed that the rs2281983 allele C and rs4919621 allele A were significantly associated with the risk of PD (all of the P values were <= 0.0001) in EOPD population. This research indicated that the presence of the rs4919621 allele A significantly increased the risk of PD patients in Caucasian population while rs2281983 allele C and rs4919621 allele A were both risk factors in EOPD. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:80 / 86
页数:7
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