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Article: Polymorphisms of CR1, CLU and PICALM confer susceptibility of Alzheimer's disease in a southern Chinese population
Title | Polymorphisms of CR1, CLU and PICALM confer susceptibility of Alzheimer's disease in a southern Chinese population |
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Authors | |
Keywords | Alzheimer's disease Chinese CLU and PICALM CR1 Genetics |
Issue Date | 2012 |
Publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/neuaging |
Citation | Neurobiology of Aging, 2012, v. 33 n. 1, p. 210.e1-210.e7 How to Cite? |
Abstract | In this case-controlled study, we tested susceptible genetic variants for Alzheimer's disease (AD) in CR1, CLU and PICALM from genome-wide association studies (GWAS) in a southern Chinese population. Eight hundred twelve participants consisting of 462 late-onset Alzheimer's disease (LOAD) patients and 350 nondemented control subjects were recruited. We found by multivariate logistic regression analysis, that single nucleotide polymorphisms (SNPs) in CR1 (rs6656401 adjusted allelic p = 0.035; adjusted genotypic p = 0.043) and CLU (rs2279590 adjusted allelic p = 0.035; adjusted genotypic p = 0.006; rs11136000 adjusted allelic p = 0.038; adjusted genotypic p = 0.009) were significantly different between LOAD patients and nondemented controls. For PICALM, LOAD association was found only in the APOE ε4 (-) subgroup (rs3851179 adjusted allelic p = 0.028; adjusted genotypic p = 0.013). Our findings showed evidence of CR1, CLU, and PICALM and LOAD susceptibility in an independent southern Chinese population, which provides additional evidence for LOAD association apart from prior genome-wide association studies in Caucasian populations. © 2012 Elsevier Inc. |
Persistent Identifier | http://hdl.handle.net/10722/147651 |
ISSN | 2023 Impact Factor: 3.7 2023 SCImago Journal Rankings: 1.488 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chen, LH | en_US |
dc.contributor.author | Kao, PYP | en_US |
dc.contributor.author | Fan, YH | en_US |
dc.contributor.author | Ho, DTY | en_US |
dc.contributor.author | Chan, CSY | en_US |
dc.contributor.author | Yik, PY | en_US |
dc.contributor.author | Ha, JCT | en_US |
dc.contributor.author | Chu, LW | en_US |
dc.contributor.author | Song, YQ | en_US |
dc.date.accessioned | 2012-05-29T06:05:14Z | - |
dc.date.available | 2012-05-29T06:05:14Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.citation | Neurobiology of Aging, 2012, v. 33 n. 1, p. 210.e1-210.e7 | en_US |
dc.identifier.issn | 0197-4580 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/147651 | - |
dc.description.abstract | In this case-controlled study, we tested susceptible genetic variants for Alzheimer's disease (AD) in CR1, CLU and PICALM from genome-wide association studies (GWAS) in a southern Chinese population. Eight hundred twelve participants consisting of 462 late-onset Alzheimer's disease (LOAD) patients and 350 nondemented control subjects were recruited. We found by multivariate logistic regression analysis, that single nucleotide polymorphisms (SNPs) in CR1 (rs6656401 adjusted allelic p = 0.035; adjusted genotypic p = 0.043) and CLU (rs2279590 adjusted allelic p = 0.035; adjusted genotypic p = 0.006; rs11136000 adjusted allelic p = 0.038; adjusted genotypic p = 0.009) were significantly different between LOAD patients and nondemented controls. For PICALM, LOAD association was found only in the APOE ε4 (-) subgroup (rs3851179 adjusted allelic p = 0.028; adjusted genotypic p = 0.013). Our findings showed evidence of CR1, CLU, and PICALM and LOAD susceptibility in an independent southern Chinese population, which provides additional evidence for LOAD association apart from prior genome-wide association studies in Caucasian populations. © 2012 Elsevier Inc. | en_US |
dc.language | eng | en_US |
dc.publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/neuaging | en_US |
dc.relation.ispartof | Neurobiology of Aging | en_US |
dc.rights | NOTICE: this is the author’s version of a work that was accepted for publication in Neurobiology of Aging. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Neurobiology of Aging, 2012, v. 33 n. 1, p. 210.e1-210.e7. DOI: 10.1016/j.neurobiolaging.2011.09.016 | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Alzheimer's disease | - |
dc.subject | Chinese | - |
dc.subject | CLU and PICALM | - |
dc.subject | CR1 | - |
dc.subject | Genetics | - |
dc.subject.mesh | Alzheimer Disease - Genetics | en_US |
dc.subject.mesh | Apolipoprotein E4 - Genetics | en_US |
dc.subject.mesh | Asian Continental Ancestry Group - Genetics | en_US |
dc.subject.mesh | Case-Control Studies | en_US |
dc.subject.mesh | Clusterin - Genetics | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Genetic Association Studies | en_US |
dc.subject.mesh | Genetic Predisposition To Disease - Genetics | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Monomeric Clathrin Assembly Proteins - Genetics | en_US |
dc.subject.mesh | Multivariate Analysis | en_US |
dc.subject.mesh | Polymorphism, Single Nucleotide | en_US |
dc.subject.mesh | Receptors, Complement 3B - Genetics | en_US |
dc.title | Polymorphisms of CR1, CLU and PICALM confer susceptibility of Alzheimer's disease in a southern Chinese population | en_US |
dc.type | Article | en_US |
dc.identifier.email | Song, YQ:songy@hkucc.hku.hk | en_US |
dc.identifier.authority | Song, YQ=rp00488 | en_US |
dc.description.nature | postprint | en_US |
dc.identifier.doi | 10.1016/j.neurobiolaging.2011.09.016 | en_US |
dc.identifier.pmid | 22015308 | - |
dc.identifier.scopus | eid_2-s2.0-81355148562 | en_US |
dc.identifier.hkuros | 205931 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-81355148562&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 33 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.spage | 210.e1 | en_US |
dc.identifier.epage | 210.e7 | en_US |
dc.identifier.eissn | 1558-1497 | - |
dc.identifier.isi | WOS:000297934700057 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Chen, LH=54584975000 | en_US |
dc.identifier.scopusauthorid | Kao, PYP=24280722500 | en_US |
dc.identifier.scopusauthorid | Fan, YH=37461378000 | en_US |
dc.identifier.scopusauthorid | Ho, DTY=54585293500 | en_US |
dc.identifier.scopusauthorid | Chan, CSY=7404813785 | en_US |
dc.identifier.scopusauthorid | Yik, PY=15060623700 | en_US |
dc.identifier.scopusauthorid | Ha, JCT=54585132200 | en_US |
dc.identifier.scopusauthorid | Chu, LW=7202236665 | en_US |
dc.identifier.scopusauthorid | Song, YQ=7404921212 | en_US |
dc.identifier.citeulike | 9949130 | - |
dc.identifier.issnl | 0197-4580 | - |