Lack of association between three single nucleotide polymorphisms in the PARK9, PARK15, and BST1 genes and Parkinson's disease in the northern Han Chinese population
查看参考文献22篇
文摘
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Background Parkinson's disease (PD) is an autosomally inherited neurodegenerative disease in elderly people. The etiology of PD has long been thought to be associated with both genetic and environmental factors. To explore potential genetic risk factors for PD in the northern Han Chinese population, we investigated three single nucleotide polymorphisms (SNPs) (rs4538475, rs11107 and rs12564040) in the BST1, PARK15 and PARK9 genes. Methods Genomic DNA from 215 PD patients and 212 matched controls was amplified in two independent PCR systems and subsequently genotyped by digestion with the endonuclease PstI. Genetic parameter and association studies were carried out with SPSS 13.0 and PLINK 1.07 software. Results We could accurately detect all genotypes in the three loci with the PCR-RFLP or mismatched PCR-RFLP techniques. The observed heterozygosities of the rs4538475 and rs11107 loci in PD and control groups ranged from 0.460–0.481 and 0.410–0.441, in BST1, PARK15 respectively, while we detected no heterozygosity at the rs12564040 locus in PARK9. The similar distributions of genotypic frequency between both groups suggest that the three SNPs investigated in this study are unlikely to play roles as common risk factors or pathogenic mutations for PD in northern Han Chinese. Conclusion The SNPs investigated in the BST1, PARK15 and PARK9 genes associated with PD susceptibility are not associated with PD in the northern Han Chinese population. |
来源
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Chinese Medical Journal
,2012,125(4):588-592 【核心库】
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DOI
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10.3760/cma.j.issn.0366-6999.2012.04.006
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关键词
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Parkinson disease
;
PARK9
;
PARK15
;
BST1
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genetic association studies
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地址
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1.
School of Forensic Medicine, China Medical University, Liaoning, Shenyang, 110001
2.
Department of Neurology, the First Hospital of China Medical University, Liaoning, Shenyang, 110001
3.
Department of Neurosurgery, Dalian University Affiliated Xinhua Hospital, Liaoning, Dalian, 116021
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语种
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英文 |
文献类型
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研究性论文 |
ISSN
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0366-6999 |
学科
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中国医学 |
基金
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supported by a grant from the National Natural Science Foundation of China
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文献收藏号
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CSCD:4440285
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参考文献 共
22
共2页
|
1.
Spencer A H. The prevalence and clinical characteristics of punding in Parkinson’s disease.
Mov Disord,2011,26:578-586
|
CSCD被引
3
次
|
|
|
|
2.
Nuytemans K. Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.
Hum Mutat,2010,31:763-780
|
CSCD被引
16
次
|
|
|
|
3.
Lesage S. Parkinson’s disease: from monogenic forms to genetic susceptibility factors.
Hum Mol Genet,2009,18:R48-R59
|
CSCD被引
24
次
|
|
|
|
4.
Saad M. Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson’s disease in the European population.
Hum Mol Genet,2011,20:615-627
|
CSCD被引
5
次
|
|
|
|
5.
International Parkinson Disease Genomics Consortium. Imputation of sequence variants for identification of genetic risks for Parkinson’s disease: a meta-analysis of genome-wide association studies.
Lancet,2011,377:641-649
|
CSCD被引
11
次
|
|
|
|
6.
Ramirez A. Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.
Nat Genet,2006,38:1184-1191
|
CSCD被引
29
次
|
|
|
|
7.
Paisan-Ruiz C. Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations.
Mov Disord,2010,25:1791-1800
|
CSCD被引
6
次
|
|
|
|
8.
Satake W. Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson’s disease.
Nat Genet,2009,41:1303-1307
|
CSCD被引
26
次
|
|
|
|
9.
Shi Q. An Ile93Met substitution in the UCH-L1 gene is not a disease-causing mutation for idiopathic Parkinson’s disease.
Chin Med J,2003,116:312-313
|
CSCD被引
2
次
|
|
|
|
10.
Wang T. Systematic examination of DNA variants in the parkin gene in patients with Parkinson’s disease.
Chin Med J,2004,117:1567-1569
|
CSCD被引
2
次
|
|
|
|
11.
Purcell S. PLINK: a tool set for whole-genome association and population-based linkage analyses.
Am J Hum Genet,2007,81:559-575
|
CSCD被引
632
次
|
|
|
|
12.
Pang H. Polymorphic analysis of the human phosphoglucomutase-3 gene based on mismatched PCR-RFLP technique.
Biochem Genet,2010,48:208-214
|
CSCD被引
1
次
|
|
|
|
13.
Pang H. Mismatched multiplex PCR amplification and subsequent RFLP analysis to simultaneously identify polymorphisms of erythrocytic ESD, GLO1, and GPT genes.
J Forensic Sci,2011,56:S176-S178
|
CSCD被引
2
次
|
|
|
|
14.
Shojaee S. Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays.
Am J Hum Genet,2008,82:1375-1384
|
CSCD被引
5
次
|
|
|
|
15.
Di Fonzo A. FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome.
Neurology,2009,72:240-245
|
CSCD被引
10
次
|
|
|
|
16.
Luo L Z. FBXO7 gene mutations may be rare in Chinese early-onset Parkinsonism patients.
Neurosci Lett,2010,482:86-89
|
CSCD被引
1
次
|
|
|
|
17.
Gitler A D. Alpha-synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicity.
Nat Genet,2009,41:308-315
|
CSCD被引
9
次
|
|
|
|
18.
Fei Q Z. Lack of association between ATP13A2 Ala746Thr variant and Parkinson’s disease in Han population of mainland China.
Neurosci Lett,2010,475:61-63
|
CSCD被引
4
次
|
|
|
|
19.
Ning Y P. PARK9-linked parkinsonism in eastern Asia: mutation detection in ATP13A2 and clinical phenotype.
Neurology,2008,70:1491-1493
|
CSCD被引
6
次
|
|
|
|
20.
Rakovic A. Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson’s disease.
Mov Disord,2009,24:429-433
|
CSCD被引
2
次
|
|
|
|
引证文献
1
篇
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1
Cui Honggang
Association of Five SNPs at the PARK16 Locus as a Susceptibility Locus with Parkinson's Disease for Forensic Application
法医学杂志,2013,29(3):185-189
CSCD被引
0
次
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