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Vitamin K epoxide reductase complex subunit 1 gene polymorphism is associated with atherothrombotic complication after drug-eluting stent implantation: 2-Center prospective cohort study

  • Jung Won Suh
  • , Sang Hong Baek
  • , Jin Shik Park
  • , Hyun Jae Kang
  • , In Ho Chae
  • , Dong Ju Choi
  • , Hun Jun Park
  • , Pum Joon Kim
  • , Ki Bae Seung
  • , Hyo Soo Kim
  • Seoul National University
  • The Catholic University of Korea

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Background: Single nucleotide polymorphisms of vitamin K epoxide reductase complex subunit 1 (VKORC1) was reported to have association with arterial vascular disease. We investigated whether single nucleotide polymorphism of VKORC1 +2255 is associated with clinical outcomes among patients who underwent drug-eluting stent (DES) implantation. Methods: We prospectively collected genomic DNA in patients who underwent DES deployment from September 2003 to December 2006 and compared clinical outcomes according to their VKORC1 genotype at the locus + 2255 (rs 2359612). The primary end point was composite of atherothrombotic events (cardiac death, myocardial infarction, and nonhemorrhagic stroke). Results: Mean follow-up duration was 631 ± 251 days. Genotyping was completed in 764 cases (TT genotype [n = 640, 83.8%] vs non-TT [CC or CT] genotype [n = 124, 16.2%]). Non-TT group showed more composite events than TT group (7.3% vs 3.0%, P = .032). In the Cox regression analysis, non-TT genotype of VKORC gene was a significant predictor of atherothrombotic events (hazard ratio 2.56, 95% confidence interval 1.14-5.78). In the event-free survival analysis, non-TT group also showed significantly poorer cardiovascular events-free survival rate than TT group (P = .02). Conclusions: VKORC1 genotype is associated with cardiovascular events in patients with DES implantation, suggesting the role of coagulation system.

Original languageEnglish
Pages (from-to)908-912
Number of pages5
JournalAmerican Heart Journal
Volume157
Issue number5
DOIs
StatePublished - May 2009

Bibliographical note

Funding Information:
This study was supported by the grants from the Korea Health 21 R&D Project, Ministry of Health and Welfare, Republic of Korea (0412-CR02-0704-0001), and the Innovative Research Institute for Cell Therapy (A062260).

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