Paraoxonase 1 (PON1) gene polymorphisms and Parkinson's disease in a Finnish population

被引:26
|
作者
Clarimon, J
Eerola, J
Hellström, I
Tienari, PJ
Singleton, A
机构
[1] NIH, Lab Neurogenet, Mol Genet Sect, Bethesda, MD 20892 USA
[2] Helsinki Univ, Cent Hosp, Dept Neurol, Helsinki, Finland
[3] Helsinki Univ, Biomed Helsinki, Neurosci Programme, Helsinki, Finland
[4] Seinajoki Cent Hosp, Dept Neurol, Seinajoki, Finland
关键词
Parkinson's disease; Finland; genetic association; PON1; polymorphism; complex disorder;
D O I
10.1016/j.neulet.2004.05.108
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Paraoxonase 1 (PON1) is involved in the metabolism and detoxification of insecticides and pesticides. Two polymorphisms within the gene affect the enzyme activity. One is a methionine to leucine change at position 54 (M54L) and the other is a glutamine to arginine variant at position 192 (Q192R). There are contrasting reports assessing the role of these variants in Parkinson's disease (PD). We performed a case-control association study in order to elucidate the possible contribution of variability within PON1 to the risk of sporadic PD in a Finnish population. There was no statistically significant association of the allele, genotype or haplotype distribution with PD (all P values > 0.75). Our results suggest that the M54L and Q192R polymorphisms are not major risk factors for PD in the Finnish population. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:168 / 170
页数:3
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