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

IMR OpenIR

	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
其他题名	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
	Zhu Lanhui 1; Luo Xiaoguang 1; Zhou Yishu 1; Li Fengrui 1; Yang Yichun 3; Ren Yan 1; Pang Hao 1
	2012
发表期刊	CHINESE MEDICAL JOURNAL
ISSN	0366-6999
卷号	125 期号:4 页码:588-592
摘要	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.
其他摘要	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.
关键词	GENOME-WIDE ASSOCIATION P-TYPE ATPASE PYRAMIDAL SYNDROME ATP13A2 MUTATIONS VARIANTS FBXO7 LOCI Parkinson disease PARK9 PARK15 BST1 genetic association studies
收录类别	CSCD
语种	英语
资助项目	[National Natural Science Foundation of China]
CSCD记录号	CSCD:4440285
引用统计	被引频次：1[CSCD] [CSCD记录]
文献类型	期刊论文
条目标识符	http://ir.imr.ac.cn/handle/321006/157450
专题	中国科学院金属研究所
作者单位	1.中国科学院金属研究所 2.Baotou Med Coll, Department Forens Med, Baotou 014060, Inner Mongolia, Peoples R China 3.大连大学
推荐引用方式 GB/T 7714	Zhu Lanhui,Luo Xiaoguang,Zhou Yishu,et al. 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[J]. CHINESE MEDICAL JOURNAL,2012,125(4):588-592.
APA	Zhu Lanhui.,Luo Xiaoguang.,Zhou Yishu.,Li Fengrui.,Yang Yichun.,...&Pang Hao.(2012).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.CHINESE MEDICAL JOURNAL,125(4),588-592.
MLA	Zhu Lanhui,et al."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".CHINESE MEDICAL JOURNAL 125.4(2012):588-592.