Source:http://linkedlifedata.com/resource/pubmed/id/19406621
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-3
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pubmed:dateCreated |
2009-6-22
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pubmed:abstractText |
A variety of evidence suggests brain-derived neurotrophic factor (BDNF) as a candidate gene for schizophrenia, and several genetic studies have shown a significant association between the disease and certain SNPs within BDNF (specifically, Val66Met and C270T). According to a recent study, the functional microsatellite marker BDNF-LCPR (BDNF-linked complex polymorphic region), which affects the expression level of BDNF, is associated with bipolar disorder. The goals of our current study were to 1) evaluate the quality of HapMap-based linkage disequilibrium (LD) tagging of BDNF-LCPR, 2) examine whether these tagging SNPs are associated with schizophrenia in a Japanese population, and 3) conduct a meta-analysis of the two most extensively studied polymorphisms: Val66Met and C270T. We genotyped eight tagging SNPs, including Val66Met and C270T. Our LD evaluation showed that BDNF-LCPR could be represented by these tagging SNPs in controls (with 73.5% allelic coverage). However, the functional A1 allele was not captured due to its low minor allele frequency (2.2%). In a case-control study (1117 schizophrenics and 1102 controls), no association was found in single-marker or multimarker analysis. Moreover, in a meta-analysis, the Val66Met polymorphism was not associated with schizophrenia, whereas C270T showed a trend for association in a fixed model (p=0.036), but not in a random model (p=0.053). From these findings, we conclude that if BDNF is indeed associated with schizophrenia, the A1 allele in BDNF-LCPR would be the most promising candidate. Further LD evaluation, as well as an association study in which BDNF-LCPR is genotyped directly, would be required for a more conclusive result.
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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 |
Jul
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pubmed:issn |
1573-2509
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pubmed:author |
pubmed-author:BrankoAleksicA,
pubmed-author:IkedaMasashiM,
pubmed-author:InadaToshiyaT,
pubmed-author:IwataNakaoN,
pubmed-author:KawashimaKunihiroK,
pubmed-author:KinoshitaYokoY,
pubmed-author:KishiTaroT,
pubmed-author:KitajimaTsuyoshiT,
pubmed-author:KunugiHiroshiH,
pubmed-author:OkadaTakeyaT,
pubmed-author:OkochiTomoT,
pubmed-author:OzakiNorioN,
pubmed-author:TomitaMakotoM,
pubmed-author:YamanouchiYoshioY
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pubmed:issnType |
Electronic
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pubmed:volume |
112
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
72-9
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pubmed:dateRevised |
2010-9-2
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pubmed:meshHeading |
pubmed-meshheading:19406621-Adult,
pubmed-meshheading:19406621-Brain-Derived Neurotrophic Factor,
pubmed-meshheading:19406621-Case-Control Studies,
pubmed-meshheading:19406621-Female,
pubmed-meshheading:19406621-Gene Frequency,
pubmed-meshheading:19406621-Genotype,
pubmed-meshheading:19406621-Humans,
pubmed-meshheading:19406621-Japan,
pubmed-meshheading:19406621-Linkage Disequilibrium,
pubmed-meshheading:19406621-Male,
pubmed-meshheading:19406621-Methionine,
pubmed-meshheading:19406621-Middle Aged,
pubmed-meshheading:19406621-Polymorphism, Single Nucleotide,
pubmed-meshheading:19406621-Schizophrenia,
pubmed-meshheading:19406621-Valine,
pubmed-meshheading:19406621-Young Adult
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pubmed:year |
2009
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pubmed:articleTitle |
BDNF is not associated with schizophrenia: data from a Japanese population study and meta-analysis.
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pubmed:affiliation |
Department of Psychiatry, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Meta-Analysis
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