Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese

The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 ( UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the UCHL1 variant in PD among ethnic...

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Published inNeurobiology of aging Vol. 31; no. 12; pp. 2194 - 2196
Main Authors Tan, E.K., Lu, C.S., Peng, R., Teo, Y.Y., Wu-Chou, Y.H., Chen, R.S., Weng, Y.H., Chen, C.M., Fung, H.C., Tan, L.C., Zhang, Z.J., An, X.K., Lee-Chen, G.J., Lee, M.C., Fook-Chong, S., Burgunder, J.M., Wu, R.M., Wu, Y.R.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.12.2010
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Abstract The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 ( UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the UCHL1 variant in PD among ethnic Chinese. Individual data sets from 5 centers comprising a total of 4088 study subjects were analyzed. In the univariate analysis, only data from 1 center showed a trend towards a protective effect among young subjects. However, in the combined analysis, no significant association between the UCHL1 variant and PD was detected (A allele frequency 0.531 vs. 0.528, p = 0.87, OR 1.01, 95% CI 0.92–1.1). Among subjects less than 60 years old, the OR is 0.99 (95% CI 0.84–1.16, p = 0.88). A multivariate logistic regression analysis showed that family history, UCHL1 variant and the interaction of UCHL1 variant and age at onset ( p = 0.816) were not significantly associated with PD.
AbstractList The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 ( UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the UCHL1 variant in PD among ethnic Chinese. Individual data sets from 5 centers comprising a total of 4088 study subjects were analyzed. In the univariate analysis, only data from 1 center showed a trend towards a protective effect among young subjects. However, in the combined analysis, no significant association between the UCHL1 variant and PD was detected (A allele frequency 0.531 vs. 0.528, p = 0.87, OR 1.01, 95% CI 0.92–1.1). Among subjects less than 60 years old, the OR is 0.99 (95% CI 0.84–1.16, p = 0.88). A multivariate logistic regression analysis showed that family history, UCHL1 variant and the interaction of UCHL1 variant and age at onset ( p = 0.816) were not significantly associated with PD.
The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 (UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the UCHL1 variant in PD among ethnic Chinese. Individual data sets from 5 centers comprising a total of 4088 study subjects were analyzed. In the univariate analysis, only data from 1 center showed a trend towards a protective effect among young subjects. However, in the combined analysis, no significant association between the UCHL1 variant and PD was detected (A allele frequency 0.531 vs. 0.528, p = 0.87, OR 1.01, 95% CI 0.92-1.1). Among subjects less than 60 years old, the OR is 0.99 (95% CI 0.84-1.16, p = 0.88). A multivariate logistic regression analysis showed that family history, UCHL1 variant and the interaction of UCHL1 variant and age at onset (p = 0.816) were not significantly associated with PD.
Abstract The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 ( UCHL1 ) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the UCHL1 variant in PD among ethnic Chinese. Individual data sets from 5 centers comprising a total of 4088 study subjects were analyzed. In the univariate analysis, only data from 1 center showed a trend towards a protective effect among young subjects. However, in the combined analysis, no significant association between the UCHL1 variant and PD was detected (A allele frequency 0.531 vs. 0.528, p = 0.87, OR 1.01, 95% CI 0.92–1.1). Among subjects less than 60 years old, the OR is 0.99 (95% CI 0.84–1.16, p = 0.88). A multivariate logistic regression analysis showed that family history, UCHL1 variant and the interaction of UCHL1 variant and age at onset ( p = 0.816) were not significantly associated with PD.
The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 (UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the UCHL1 variant in PD among ethnic Chinese. Individual data sets from 5 centers comprising a total of 4088 study subjects were analyzed. In the univariate analysis, only data from 1 center showed a trend towards a protective effect among young subjects. However, in the combined analysis, no significant association between the UCHL1 variant and PD was detected (A allele frequency 0.531 vs. 0.528, p=0.87, OR 1.01, 95% CI 0.92-1.1). Among subjects less than 60 years old, the OR is 0.99 (95% CI 0.84-1.16, p=0.88). A multivariate logistic regression analysis showed that family history, UCHL1 variant and the interaction of UCHL1 variant and age at onset (p=0.816) were not significantly associated with PD.The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 (UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the UCHL1 variant in PD among ethnic Chinese. Individual data sets from 5 centers comprising a total of 4088 study subjects were analyzed. In the univariate analysis, only data from 1 center showed a trend towards a protective effect among young subjects. However, in the combined analysis, no significant association between the UCHL1 variant and PD was detected (A allele frequency 0.531 vs. 0.528, p=0.87, OR 1.01, 95% CI 0.92-1.1). Among subjects less than 60 years old, the OR is 0.99 (95% CI 0.84-1.16, p=0.88). A multivariate logistic regression analysis showed that family history, UCHL1 variant and the interaction of UCHL1 variant and age at onset (p=0.816) were not significantly associated with PD.
Author An, X.K.
Burgunder, J.M.
Wu, Y.R.
Wu-Chou, Y.H.
Lu, C.S.
Tan, E.K.
Tan, L.C.
Fook-Chong, S.
Weng, Y.H.
Chen, C.M.
Chen, R.S.
Wu, R.M.
Lee, M.C.
Fung, H.C.
Peng, R.
Zhang, Z.J.
Lee-Chen, G.J.
Teo, Y.Y.
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  email: yihruwu@adm.cgmh.org.tw
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10.1002/mds.21064
10.1016/j.neulet.2008.07.012
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Issue 12
Keywords UCHL1
Parkinson's disease
Polymorphism
Language English
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Snippet The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 ( UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian...
Abstract The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 ( UCHL1 ) S18Y variant with Parkinson's disease (PD) among Caucasian...
The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 (UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian...
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StartPage 2194
SubjectTerms Adolescent
Adult
Age of Onset
Aged
Aged, 80 and over
Asian Continental Ancestry Group - ethnology
Asian Continental Ancestry Group - genetics
Female
Genetic Association Studies
Genetic Variation - genetics
Humans
Internal Medicine
Male
Middle Aged
Neurology
Parkinson Disease - enzymology
Parkinson Disease - epidemiology
Parkinson Disease - genetics
Parkinson's disease
Polymorphism
Singapore - epidemiology
Singapore - ethnology
Taiwan - epidemiology
Taiwan - ethnology
Ubiquitin Thiolesterase - genetics
Ubiquitination - genetics
UCHL1
Young Adult
Title Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0197458008004041
https://www.clinicalkey.es/playcontent/1-s2.0-S0197458008004041
https://dx.doi.org/10.1016/j.neurobiolaging.2008.11.008
https://www.ncbi.nlm.nih.gov/pubmed/19329225
https://www.proquest.com/docview/759879192
https://www.proquest.com/docview/899137019
Volume 31
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