RGD Reference Report - Identification of a polymorphism of UCP3 associated with recurrent in-stent restenosis of coronary arteries. - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Identification of a polymorphism of UCP3 associated with recurrent in-stent restenosis of coronary arteries.

Authors: Oguri, M  Kato, K  Hibino, T  Yokoi, K  Segawa, T  Matsuo, H  Watanabe, S  Nozawa, Y  Murohara, T  Yamada, Y 
Citation: Oguri M, etal., Int J Mol Med. 2007 Oct;20(4):533-8.
RGD ID: 2313513
Pubmed: PMID:17786284   (View Abstract at PubMed)

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.



RGD Manual Disease Annotations    Click to see Annotation Detail View

  
Object SymbolSpeciesTermQualifierEvidenceWithNotesSourceOriginal Reference(s)
UCP3Humancoronary restenosis susceptibilityIAGP DNA:polymorphism:promoter:-55C>T (human)RGD 
Ucp3Ratcoronary restenosis susceptibilityISOUCP3 (Homo sapiens)DNA:polymorphism:promoter:-55C>T (human)RGD 
Ucp3Mousecoronary restenosis susceptibilityISOUCP3 (Homo sapiens)DNA:polymorphism:promoter:-55C>T (human)RGD 

Objects Annotated

Genes (Rattus norvegicus)
Ucp3  (uncoupling protein 3)

Genes (Mus musculus)
Ucp3  (uncoupling protein 3 (mitochondrial, proton carrier))

Genes (Homo sapiens)
UCP3  (uncoupling protein 3)


Additional Information