Lack of association between CYP1A1 polymorphism and Parkinson's disease in a Chinese population

被引:17
作者
Chan, DKY [1 ]
Mellick, GD
Buchanan, DD
Hung, WT
Ng, PW
Woo, J
Kay, R
机构
[1] Bankstown Hosp, Dept Aged Care & Rehabil, Bankstown, NSW 2200, Australia
[2] Princess Alexandra Hosp, Dept Med, Woolloongabba, Qld 4102, Australia
[3] Univ Technol, Key Univ Res Strength Hlth Technol, Broadway, NSW, Australia
[4] United Christian Hosp, Dept Med & Geriatr, Hong Kong, Hong Kong, Peoples R China
[5] Chinese Univ Hong Kong, Dept Med, Hong Kong, Hong Kong, Peoples R China
关键词
Parkinson's disease; polymorphism; CYP1A1; candidate gene;
D O I
10.1007/s702-002-8234-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Apart from very few families who have a direct cause from genetic mutation, causes of most Parkinson's disease (PD) remain unclear. Many allelic association studies on polymorphism of different candidate genes have been studied. Although these association studies do not imply a causal relationship, it does warrant further studies to elucidate the pathophysiologic significance. CYP1A1 polymorphisms have been reported to be associated with PD in a Japanese population sample. Since CYP1A1 transforms aromatic hydrocarbons into products that may be neurotoxic and perhaps lead to PD, we therefore undertook a study to look at the possible association of CYP1A1 polymorphism and PD in a Chinese population. Contrary to the Japanese result, we did not find any statistically significant difference between the PD group and the control group in our study with a bigger sample size.
引用
收藏
页码:35 / 39
页数:5
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