Document Detail


Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease.
MedLine Citation:
PMID:  22322877     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Chromosome 9p21 single nucleotide polymorphisms (SNPs) have been shown to be associated with coronary heart disease in multiple studies. The aim of the present study was to identify whether these SNPs are associated with recurrent myocardial infarction (MI), revascularization, or death in acute coronary syndrome (ACS) patients or in those undergoing coronary artery bypass grafting (CABG).
METHODS AND RESULTS: TexGen registry participants with ACS (n=2,067) or CABG (n=1,176) were evaluated, to assess whether 9p21 SNPs (rs1333049, rs2383206, rs10757278, rs10757274) were associated with recurrent MI (primary outcome), recurrent revascularization, or death (secondary outcomes) at approximately 3.2 years of follow-up. Carriers of risk allele (C) for rs1333049 presented at an earlier age (62 vs. 63.5 years in non-carriers, P=0.0004) with more extensive disease (number of vessels with significant stenosis: 1.9 vs. 1.7 in non-carriers, P=0.001) in the ACS group. In adjusted models, the C allele was not associated with recurrent MI (hazard ratio [HR], 1.01; 95% confidence interval [CI]: 0.74-1.38), recurrent revascularization (HR, 0.98; 95%CI: 0.78-1.23), or death (HR, 0.91; 95%CI: 0.69-1.18) in the ACS or CABG groups (recurrent MI: HR, 0.64; 95%CI: 0.40-1.05; recurrent revascularization: HR, 0.98; 95%CI: 0.61-1.55; death: HR, 0.89; 95%CI: 0.61-1.30). Results were similar for the other 3 SNPs.
CONCLUSIONS: 9p21 SNPs were not associated with recurrent MI, revascularization, or mortality after ACS or CABG. Individuals with the rs1333049 C allele, however, may present with earlier and more extensive disease.
Authors:
Salim S Virani; Ariel Brautbar; Vei-Vei Lee; Elayda MacArthur; Alanna C Morrison; Megan L Grove; Vijay Nambi; Lorraine Frazier; James M Wilson; James T Willerson; Eric Boerwinkle; Christie M Ballantyne
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.     Date:  2012-02-09
Journal Detail:
Title:  Circulation journal : official journal of the Japanese Circulation Society     Volume:  76     ISSN:  1347-4820     ISO Abbreviation:  Circ. J.     Publication Date:  2012  
Date Detail:
Created Date:  2012-03-27     Completed Date:  2012-06-25     Revised Date:  2013-12-08    
Medline Journal Info:
Nlm Unique ID:  101137683     Medline TA:  Circ J     Country:  Japan    
Other Details:
Languages:  eng     Pagination:  950-6     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Aged
Chromosomes, Human, Pair 9*
Coronary Artery Bypass / adverse effects,  mortality
Coronary Artery Disease / complications,  genetics*,  mortality,  surgery
Disease-Free Survival
Female
Gene Frequency
Genetic Predisposition to Disease
Humans
Kaplan-Meier Estimate
Male
Middle Aged
Myocardial Infarction / genetics*,  mortality,  surgery
Phenotype
Polymorphism, Single Nucleotide*
Proportional Hazards Models
Recurrence
Registries
Risk Assessment
Risk Factors
Severity of Illness Index
Texas
Time Factors
Treatment Outcome
Grant Support
ID/Acronym/Agency:
1R01NR010235-01A1/NR/NINR NIH HHS; R01 NR010235/NR/NINR NIH HHS; UL1 RR024148/RR/NCRR NIH HHS
Comments/Corrections

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