Literature DB >> 25452228

Validating GWAS-Identified Risk Loci for Alzheimer's Disease in Han Chinese Populations.

Hui-Zhen Wang1,2, Rui Bi1,3, Qiu-Xiang Hu1,3, Qun Xiang1,3, Chen Zhang4, Deng-Feng Zhang1,3, Wen Zhang1,3, Xiaohong Ma5,6, Wanjun Guo5,6, Wei Deng5,6, Liansheng Zhao5,6, Peiyan Ni5,6, Mingli Li5,6, Yiru Fang4, Tao Li5,6, Yong-Gang Yao7,8,9,10.   

Abstract

In recent years, genome-wide association studies (GWASs) have identified many novel susceptible genes/loci for Alzheimer's disease (AD). However, most of these studies were conducted in European and populations of European origin, and limited studies have been performed in Han Chinese. In this study, we genotyped 14 single-nucleotide polymorphisms (SNPs) in eight GWAS-reported AD risk genes in 1509 individuals comprising two independent Han Chinese case-control cohorts. Four SNPs (rs11234495, rs592297, rs676733, and rs3851179) in the PICALM gene were significantly associated with late-onset (LO)-AD in populations from Southwest China, whereas SNPs rs744373 (BIN1), rs9331942 (CLU), and rs670139 (MS4A4E) were linked to LO-AD in populations from East China. In the combined Han Chinese population, positive associations were observed between PICALM, CLU, MS4A4E genes, and LO-AD. The association between rs3851179 (PICALM), rs744373 (BIN1), and AD was further confirmed by meta-analysis of Asian populations. Our study verified the association between PICALM, BIN1, CLU, and MS4A4E variants and AD susceptibility in Han Chinese populations. We also discerned some regional differences concerning AD susceptibility SNPs.

Entities:  

Keywords:  Alzheimer’s disease; GWAS; Han Chinese; Variants

Mesh:

Substances:

Year:  2014        PMID: 25452228     DOI: 10.1007/s12035-014-9015-z

Source DB:  PubMed          Journal:  Mol Neurobiol        ISSN: 0893-7648            Impact factor:   5.590


  43 in total

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7.  PICALM gene rs3851179 polymorphism contributes to Alzheimer's disease in an Asian population.

Authors:  Guiyou Liu; Shuyan Zhang; Zhiyou Cai; Guoda Ma; Liangcai Zhang; Yongshuai Jiang; Rennan Feng; Mingzhi Liao; Zugen Chen; Bin Zhao; Keshen Li
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Journal:  Transl Psychiatry       Date:  2012-05-15       Impact factor: 6.222

10.  Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology.

Authors:  J Chapuis; F Hansmannel; M Gistelinck; A Mounier; C Van Cauwenberghe; K V Kolen; F Geller; Y Sottejeau; D Harold; P Dourlen; B Grenier-Boley; Y Kamatani; B Delepine; F Demiautte; D Zelenika; N Zommer; M Hamdane; C Bellenguez; J-F Dartigues; J-J Hauw; F Letronne; A-M Ayral; K Sleegers; A Schellens; L V Broeck; S Engelborghs; P P De Deyn; R Vandenberghe; M O'Donovan; M Owen; J Epelbaum; M Mercken; E Karran; M Bantscheff; G Drewes; G Joberty; D Campion; J-N Octave; C Berr; M Lathrop; P Callaerts; D Mann; J Williams; L Buée; I Dewachter; C Van Broeckhoven; P Amouyel; D Moechars; B Dermaut; J-C Lambert
Journal:  Mol Psychiatry       Date:  2013-02-12       Impact factor: 15.992

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  31 in total

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2.  A Weighted Genetic Risk Score Based on Four APOE-Independent Alzheimer's Disease Risk Loci May Supplement APOE E4 for Better Disease Prediction.

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6.  Correlation of PICALM polymorphism rs3851179 with Alzheimer's disease among Caucasian and Chinese populations: a meta-analysis and systematic review.

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10.  Meta-analysis of the Association between Alzheimer Disease and Variants in GAB2, PICALM, and SORL1.

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