Genetic variants in CCNB1 associated with differential gene transcription and risk of coronary in-stent restenosis

Circ Cardiovasc Genet. 2014 Feb;7(1):59-70. doi: 10.1161/CIRCGENETICS.113.000305. Epub 2014 Jan 5.


Background: The development of diagnostic tools to assess restenosis risk after stent deployment may enable the intervention to be tailored to the individual patient, for example, by targeting the use of drug-eluting stent to high-risk patients, with the goal of improving safety and reducing costs. The CCNB1 gene (encoding cyclin B1) positively regulates cell proliferation, a key component of in-stent restenosis. Therefore, we hypothesized that single-nucleotide polymorphisms in CCNB1 may serve as useful tools in risk stratification for in-stent restenosis.

Methods and results: We identified 3 single-nucleotide polymorphisms in CCNB1 associated with increased restenosis risk in a cohort of 284 patients undergoing coronary angioplasty and stent placement (rs350099: TT versus CC+TC; odds ratio [OR], 1.82; 95% confidence interval [CI], 1.09-3.03; P=0.023; rs350104: CC versus CT+TT; OR, 1.82; 95% CI, 1.02-3.26; P=0.040; and rs164390: GG versus GT+TT; OR, 2.27; 95% CI, 1.33-3.85; P=0.002). These findings were replicated in another cohort study of 715 patients (rs350099: TT versus CC+TC; OR, 1.88; 95% CI, 0.92-3.81; P=0.080; rs350104: CC versus CT+TT; OR, 2.23; 95% CI, 1.18-4.25; P=0.016; and rs164390: GG versus GT+TT; OR, 1.87; 95% CI, 1.03-3.47; P=0.040). Moreover, the haplotype containing all 3 risk alleles is associated with higher CCNB1 mRNA expression in circulating lymphocytes and increased in-stent restenosis risk (OR, 1.43; 95% CI, 1.00-1.823; P=0.039). The risk variants of rs350099, rs350104, and rs164390 are associated with increased reporter gene expression through binding of transcription factors nuclear factor-Y, activator protein 1, and specificity protein 1, respectively.

Conclusions: Allele-dependent transcriptional regulation of CCNB1 associated with rs350099, rs350104, and rs164390 affects the risk of in-stent restenosis. These findings reveal these common genetic variations as attractive diagnostic tools in risk stratification for restenosis.

Keywords: AP-1 transcription factor; NF–Y transcription factor; SP1 transcription factor; in-stent restenosis; polymorphism, genetics; stents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • CCAAT-Binding Factor / genetics
  • CCAAT-Binding Factor / metabolism
  • Cohort Studies
  • Coronary Angiography
  • Coronary Restenosis / etiology
  • Coronary Restenosis / genetics*
  • Coronary Restenosis / mortality
  • Cyclin B1 / genetics*
  • Cyclin B1 / metabolism
  • Drug-Eluting Stents*
  • Genotype
  • Haplotypes
  • Humans
  • Kaplan-Meier Estimate
  • Odds Ratio
  • Polymorphism, Single Nucleotide
  • Proportional Hazards Models
  • RNA, Messenger / metabolism
  • Risk Factors
  • Sp1 Transcription Factor / genetics
  • Sp1 Transcription Factor / metabolism
  • Transcription Factor AP-1 / genetics
  • Transcription Factor AP-1 / metabolism
  • Transcription, Genetic


  • CCAAT-Binding Factor
  • CCNB1 protein, human
  • Cyclin B1
  • RNA, Messenger
  • Sp1 Transcription Factor
  • Transcription Factor AP-1