Source:http://linkedlifedata.com/resource/pubmed/id/21059344
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
2011-1-3
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pubmed:abstractText |
Neural precursor cell-expressed, developmentally downregulated 9 (NEDD9) has been suspected to be associated with Alzheimer's disease (AD) through participating in the formation of neurite-like membrane extensions and neurite outgrowth to affect the number of neuronal cells/synapses in the brain under stressful conditions. A recent large-scale, multi-tiered association study has identified significant association of a common single nucleotide polymorphism (SNP) rs760678 in the NEDD9 gene with predisposition to late-onset Alzheimer's disease (LOAD) in Caucasians. In order to evaluate the involvement of the NEDD9 polymorphism in the risk of sporadic LOAD, we performed an independent case-control association study to analyze the genotype and allele distributions of the NEDD9 rs760678 polymorphism in a Han Chinese population (383 LOAD cases and 369 healthy controls). There were significant differences in genotype and allele frequencies between LOAD cases and controls (genotype P=0.003, allele P=0.002). After stratification by APOE ?4-carrying status, the C allele of rs760678 was only significantly associated with LOAD in non-APOE ?4 allele carriers (OR=1.43, 95%, CI=1.06-1.94, P=0.024). In addition, a logistic regression analysis also conferred positive association between the SNP rs760678 and LOAD (dominant model: OR=2.10, 95% CI=1.23-3.58, P=0.007; additive model: OR=1.37, 95% CI=1.09-1.74, P=0.008) after adjustment for age, gender, and the APOE ?4 carrier status. The study demonstrated a significant association between the tested SNP and LOAD, indicating that NEDD9 polymorphism has a possible role in changing the genetic susceptibility to LOAD in a Han Chinese population.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1872-6240
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Elsevier B.V. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
19
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pubmed:volume |
1369
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
230-4
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pubmed:meshHeading |
pubmed-meshheading:21059344-Adaptor Proteins, Signal Transducing,
pubmed-meshheading:21059344-Age of Onset,
pubmed-meshheading:21059344-Aged,
pubmed-meshheading:21059344-Alzheimer Disease,
pubmed-meshheading:21059344-Asian Continental Ancestry Group,
pubmed-meshheading:21059344-Case-Control Studies,
pubmed-meshheading:21059344-Female,
pubmed-meshheading:21059344-Gene Frequency,
pubmed-meshheading:21059344-Genetic Predisposition to Disease,
pubmed-meshheading:21059344-Genotype,
pubmed-meshheading:21059344-Humans,
pubmed-meshheading:21059344-Male,
pubmed-meshheading:21059344-Phosphoproteins,
pubmed-meshheading:21059344-Polymorphism, Genetic
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pubmed:year |
2011
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pubmed:articleTitle |
NEDD9 is genetically associated with Alzheimer's disease in a Han Chinese population.
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pubmed:affiliation |
Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, No.5 Donghai Middle Road, Qingdao, Shandong Province 266071, PR China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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