共 19 条
Case-control study of UCHL1 S18Y variant in Parkinson's disease
被引:25
作者:

Tan, Eng-King
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机构: Natl Inst Neurosci, Singapore Gen Hosp, Dept Neurol, SingHlth, Singapore, Singapore

Puong, Kim-Yoong
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机构: Natl Inst Neurosci, Singapore Gen Hosp, Dept Neurol, SingHlth, Singapore, Singapore

Fook-Chong, Stephanie
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机构: Natl Inst Neurosci, Singapore Gen Hosp, Dept Neurol, SingHlth, Singapore, Singapore

Chua, Eva
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机构: Natl Inst Neurosci, Singapore Gen Hosp, Dept Neurol, SingHlth, Singapore, Singapore

Shen, Hui
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h-index: 0
机构: Natl Inst Neurosci, Singapore Gen Hosp, Dept Neurol, SingHlth, Singapore, Singapore

Yuen, Yih
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机构: Natl Inst Neurosci, Singapore Gen Hosp, Dept Neurol, SingHlth, Singapore, Singapore

Pavanni, Ratnagopal
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机构: Natl Inst Neurosci, Singapore Gen Hosp, Dept Neurol, SingHlth, Singapore, Singapore

Wong, Meng-Cheong
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机构: Natl Inst Neurosci, Singapore Gen Hosp, Dept Neurol, SingHlth, Singapore, Singapore

Puvan, Kathiravelu
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机构: Natl Inst Neurosci, Singapore Gen Hosp, Dept Neurol, SingHlth, Singapore, Singapore

Zhao, Yi
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机构: Natl Inst Neurosci, Singapore Gen Hosp, Dept Neurol, SingHlth, Singapore, Singapore
机构:
[1] Natl Inst Neurosci, Singapore Gen Hosp, Dept Neurol, SingHlth, Singapore, Singapore
[2] Natl Inst Neurosci, Singapore, Singapore
[3] SingHlth Res, Singapore, Singapore
[4] Singapore Gen Hosp, Dept Clin Res, Singapore 0316, Singapore
[5] Singapore Gen Hosp, Dept Hlth Screening, Singapore 0316, Singapore
关键词:
Parkinson's disease;
UCHL1;
polymorphism;
survival;
D O I:
10.1002/mds.21064
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
A recent meta-analysis observed a greater significant inverse association of the ubiquitin carboxy-terminal hydrolase L1 (UCHL1) S18Y variant with Parkinson's disease (PD) for Asian (predominantly Japanese) populations compared with Caucasian populations. We performed an independent case-control study in 335 PD and 341 control subjects with data from a Chinese population to investigate the age-of-onset effect of the UCHL1 variant in PD. The Y/Y and Y/S genotypes were less frequent in the PD young-onset group than in controls and the frequency of the Y alleles was higher in young controls compared to young-onset PD (age at examination <= 65 years; P = 0.003). Multivariate analysis revealed the Y/Y genotype was significantly lower (P = 0.008) in the young-onset PD (Y/Y vs. S/S: odds ratio [OR]: 0.42; 95% confidence interval [Cl]: 0.24,0.74; S/Y vs. S/S: OR: 0.66, 95% Cl: 0.41, 1.08) compared with controls, but this difference was not seen for the late-onset PD. Kaplan-Meier analysis carried out on PD subjects demonstrated that the Y/Y genotype was associated with a later onset of PD than Y/S plus S/S genotypes (P = 0.05). We provided an independent confirmation of the protective effect of the UCHL1S18Y variant (Y/Y genotype) against PD in young Chinese subjects. Further functional studies of the S18Y variant in both cell and animal models will be of interest. (C) 2006 Movement Disorder Society.
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页码:1765 / 1768
页数:4
相关论文
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