Source:http://linkedlifedata.com/resource/pubmed/id/17786284
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2007-9-5
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pubmed:abstractText |
The purpose of the present study was to identify gene polymorphisms that confer susceptibility to recurrent restenosis after bare-metal stenting of coronary arteries, and thereby to assess the genetic risk for this condition. The study population comprised 527 unrelated Japanese individuals, including 28 subjects who developed in-stent restenosis two or more times and 499 subjects without restenosis. The genotypes for 142 polymorphisms of 121 candidate genes were determined with a method that combines the polymerase chain reaction and sequence-specific oligonucleotide probes with suspension array technology. Eleven polymorphisms were related (P<0.05) to the prevalence of recurrent in-stent restenosis as determined by the Chi-square test. Multivariable logistic regression analysis with adjustment for age, sex, body mass index, and the prevalence of smoking, hypertension, diabetes mellitus, and hypercholesterolemia revealed that the -55Cright curved arrow T polymorphism of the uncoupling protein 3 gene (UCP3) was significantly (P=0.0006 in a recessive model) associated with the prevalence of recurrent in-stent restenosis, with the T allele representing a risk factor for this condition. A stepwise forward selection procedure showed that the UCP3 genotype significantly (P=0.0014, recessive model) affected the prevalence of recurrent in-stent restenosis. Determination of the genotype for UCP3 may thus contribute to assessment of the genetic risk for recurrent in-stent restenosis.
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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 |
Oct
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pubmed:issn |
1107-3756
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pubmed:author |
pubmed-author:HibinoTakeshiT,
pubmed-author:KatoKimihikoK,
pubmed-author:MatsuoHitoshiH,
pubmed-author:MuroharaToyoakiT,
pubmed-author:NozawaYoshinoriY,
pubmed-author:OguriMitsutoshiM,
pubmed-author:SegawaTomonoriT,
pubmed-author:WatanabeSachiroS,
pubmed-author:YamadaYoshijiY,
pubmed-author:YokoiKiyoshiK
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pubmed:issnType |
Print
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
533-8
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pubmed:meshHeading |
pubmed-meshheading:17786284-Aged,
pubmed-meshheading:17786284-Chi-Square Distribution,
pubmed-meshheading:17786284-Coronary Restenosis,
pubmed-meshheading:17786284-Coronary Vessels,
pubmed-meshheading:17786284-Female,
pubmed-meshheading:17786284-Genetic Predisposition to Disease,
pubmed-meshheading:17786284-Humans,
pubmed-meshheading:17786284-Ion Channels,
pubmed-meshheading:17786284-Lipids,
pubmed-meshheading:17786284-Male,
pubmed-meshheading:17786284-Mitochondrial Proteins,
pubmed-meshheading:17786284-Polymorphism, Genetic,
pubmed-meshheading:17786284-Recurrence,
pubmed-meshheading:17786284-Regression Analysis,
pubmed-meshheading:17786284-Stents
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pubmed:year |
2007
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pubmed:articleTitle |
Identification of a polymorphism of UCP3 associated with recurrent in-stent restenosis of coronary arteries.
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pubmed:affiliation |
Department of Cardiovascular Medicine, Gifu Prefectural Tajimi Hospital, Tajimi, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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