Case-control study of UCHL1 S18Y variant in Parkinson's disease

被引:25
作者
Tan, Eng-King
Puong, Kim-Yoong
Fook-Chong, Stephanie
Chua, Eva
Shen, Hui
Yuen, Yih
Pavanni, Ratnagopal
Wong, Meng-Cheong
Puvan, Kathiravelu
Zhao, Yi
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.
引用
收藏
页码:1765 / 1768
页数:4
相关论文
共 19 条
[1]   S18Y polymorphism in the UCH-L1 gene and Parkinson's disease:: Evidence for an age-dependent relationship [J].
Elbaz, A ;
Levecque, C ;
Clavel, J ;
Vidal, JS ;
Richard, F ;
Corrèze, JR ;
Delemotte, B ;
Amouyel, P ;
Alpérovitch, A ;
Chartier-Harlin, MC ;
Tzourio, C .
MOVEMENT DISORDERS, 2003, 18 (02) :130-137
[2]   UCHL1 is associated with Parkinson's disease: A case-unaffected sibling and case-unrelated control study [J].
Facheris, M ;
Strain, KJ ;
Lesnick, TG ;
de Andrade, M ;
Bower, JH ;
Ahlskog, JE ;
Cunningham, JM ;
Lincoln, S ;
Farrer, MJ ;
Rocca, WA ;
Maraganore, DM .
NEUROSCIENCE LETTERS, 2005, 381 (1-2) :131-134
[3]   UCHL-1 is not a Parkinson's disease susceptibility gene [J].
Healy, DG ;
Abou-Sleiman, PM ;
Casas, JP ;
Ahmadi, KR ;
Lynch, T ;
Gandhi, S ;
Muqit, MMK ;
Foltynie, T ;
Barker, R ;
Bhatia, KP ;
Quinn, NP ;
Lees, AJ ;
Gibson, JM ;
Holton, JL ;
Revesz, T ;
Goldstein, DB ;
Wood, NW .
ANNALS OF NEUROLOGY, 2006, 59 (04) :627-633
[4]   New aspects of genetic contributions to Parkinson's disease [J].
Hofer, A ;
Gasser, T .
JOURNAL OF MOLECULAR NEUROSCIENCE, 2004, 24 (03) :417-423
[5]   The ubiquitin pathway in Parkinson's disease [J].
Leroy, E ;
Boyer, R ;
Auburger, G ;
Leube, B ;
Ulm, G ;
Mezey, E ;
Harta, G ;
Brownstein, MJ ;
Jonnalagada, S ;
Chernova, T ;
Dehejia, A ;
Lavedan, C ;
Gasser, T ;
Steinbach, PJ ;
Wilkinson, KD ;
Polymeropoulos, MH .
NATURE, 1998, 395 (6701) :451-452
[6]   No genetic association of the Ubiquitin Carboxy-terminal Hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease [J].
Levecque, C ;
Destée, A ;
Mouroux, V ;
Becquet, E ;
Defebvre, L ;
Amouyel, P ;
Chartier-Harlin, MC .
JOURNAL OF NEURAL TRANSMISSION, 2001, 108 (8-9) :979-984
[7]   The UCH-L1 gene encodes two opposing enzymatic activities that affect α-synuclein degradation and Parkinson's disease susceptibility [J].
Liu, YC ;
Fallon, L ;
Lashuel, HA ;
Liu, ZH ;
Lansbury, PT .
CELL, 2002, 111 (02) :209-218
[8]   Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease [J].
Maraganore, DM ;
Farrer, MJ ;
Hardy, JA ;
Lincoln, SJ ;
McDonnell, SK ;
Rocca, WA .
NEUROLOGY, 1999, 53 (08) :1858-1860
[9]   UCHL1 is a Parkinson's disease susceptibility gene [J].
Maraganore, DM ;
Lesnick, TG ;
Elbaz, A ;
Chartier-Harlin, MC ;
Gasser, T ;
Krüger, R ;
Hattori, N ;
Mellick, GD ;
Quattrone, A ;
Satoh, J ;
Toda, T ;
Wang, J ;
Ioannidis, JPA ;
de Andrade, M ;
Rocca, WA .
ANNALS OF NEUROLOGY, 2004, 55 (04) :512-521
[10]   The ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism does not confer protection against idiopathic Parkinson's disease [J].
Mellick, GD ;
Silburn, PA .
NEUROSCIENCE LETTERS, 2000, 293 (02) :127-130