Source:http://linkedlifedata.com/resource/pubmed/id/20043139
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
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| pubmed:dateCreated |
2009-12-31
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| pubmed:abstractText |
Although metabolic syndrome has been recognized as a risk factor for ischemic stroke, genetic factors associated with ischemic stroke in individuals with metabolic syndrome remain unknown. We examined an association of genetic variants with ischemic stroke among individuals with or without metabolic syndrome. The study population comprised 4,387 unrelated Japanese individuals, including 1,884 individuals with metabolic syndrome (240 subjects with ischemic stroke and 1,644 controls) and 2,503 individuals without metabolic syndrome (280 subjects with ischemic stroke and 2,223 controls). The 150 polymorphisms examined in the present study were selected by genome-wide association studies of ischemic stroke and myocardial infarction with the use of the GeneChip Human Mapping 500K Array Set (Affymetrix). The initial chi-square test revealed that the Cright curved arrow T polymorphism (rs9925481) of CLEC16A and the Aright curved arrow G polymorphism (rs4923918) of SPTBN5 were significantly (P<0.005) associated with ischemic stroke among individuals with metabolic syndrome. No polymorphism was significantly associated with ischemic stroke among individuals without metabolic syndrome. Multivariable logistic regression analysis with adjustment for covariates and a stepwise forward selection procedure revealed that the Aright curved arrow G polymorphism (rs4923918) of SPTBN5 was significantly (P<0.005), and the Cright curved arrow T polymorphism (rs9925481) of CLEC16A was almost significantly, associated with ischemic stroke in individuals with metabolic syndrome. Genetic variants that confer susceptibility to ischemic stroke may differ among individuals with or without metabolic syndrome. Stratification of subjects according to the presence or absence of metabolic syndrome may thus be important for personalized prevention of ischemic stroke based on genetic information.
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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 |
Feb
|
| pubmed:issn |
1791-244X
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| pubmed:author |
pubmed-author:AoyagiYukitoshiY,
pubmed-author:KatoKimihikoK,
pubmed-author:MetokiNorifumiN,
pubmed-author:NozawaYoshinoriY,
pubmed-author:OguriMitsutoshiM,
pubmed-author:SatohKeiK,
pubmed-author:WatanabeSachiroS,
pubmed-author:YamadaYoshijiY,
pubmed-author:YokoiKiyoshiK,
pubmed-author:YoshidaHidemiH,
pubmed-author:YoshidaTetsuroT
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| pubmed:issnType |
Electronic
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| pubmed:volume |
25
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| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
281-6
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| pubmed:dateRevised |
2010-5-20
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| pubmed:meshHeading |
pubmed-meshheading:20043139-Aged,
pubmed-meshheading:20043139-Brain Ischemia,
pubmed-meshheading:20043139-Chi-Square Distribution,
pubmed-meshheading:20043139-Female,
pubmed-meshheading:20043139-Genetic Predisposition to Disease,
pubmed-meshheading:20043139-Genetic Variation,
pubmed-meshheading:20043139-Humans,
pubmed-meshheading:20043139-Hypertension,
pubmed-meshheading:20043139-Japan,
pubmed-meshheading:20043139-Lectins, C-Type,
pubmed-meshheading:20043139-Male,
pubmed-meshheading:20043139-Metabolic Syndrome X,
pubmed-meshheading:20043139-Middle Aged,
pubmed-meshheading:20043139-Monosaccharide Transport Proteins,
pubmed-meshheading:20043139-Polymorphism, Single Nucleotide,
pubmed-meshheading:20043139-Regression Analysis,
pubmed-meshheading:20043139-Spectrin,
pubmed-meshheading:20043139-Stroke
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| pubmed:year |
2010
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| pubmed:articleTitle |
Association of genetic variants with ischemic stroke in Japanese individuals with or without metabolic syndrome.
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| pubmed:affiliation |
Department of Cardiovascular Medicine, Inabe General Hospital, Inabe, Japan.
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| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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