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Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China
- Source :
- Neuroscience Letters. 475:61-63
- Publication Year :
- 2010
- Publisher :
- Elsevier BV, 2010.
-
Abstract
- ATP13A2 (PARK9) mutations are related to Kufor-Rakeb syndrome (KRS). We performed genetic analysis of the Ala746Thr variant in an independent cohort of the patients with PD and healthy controls from mainland China. The Ala746Thr variant was present in 1/532 (0.19%) of PD compared with 1/480 (0.21%) of healthy controls (odds ratio=0.90, 95% CI 0.06, 14.39, P=1.00). The two subjects carried the heterozygous genotype. Subset analysis in the group/=50 years of age revealed a prevalence of 0.7% in PD compared with 0% in healthy controls and in the group50 years of age showed 0% in PD versus 0.3% in healthy controls. We did not observe a significant association between Ala746Thr and Parkinson's disease in Han Chinese population, even after stratification by age at onset. The results suggested that Ala746Thr variant was not a major susceptible factor for PD in Han Chinese people.
- Subjects :
- Adult
Male
Subset Analysis
China
medicine.medical_specialty
Pathology
Single-nucleotide polymorphism
Genome-wide association study
Young Adult
Asian People
Internal medicine
Genetic variation
Genotype
Humans
Medicine
Genetic Predisposition to Disease
Aged
Aged, 80 and over
business.industry
General Neuroscience
Haplotype
Parkinson Disease
Odds ratio
Middle Aged
Proton-Translocating ATPases
Mutation
Cohort
Female
business
Genome-Wide Association Study
Subjects
Details
- ISSN :
- 03043940
- Volume :
- 475
- Database :
- OpenAIRE
- Journal :
- Neuroscience Letters
- Accession number :
- edsair.doi.dedup.....f7511f1b7b945d05b7603451de7b82f2