Polymorphism K469E of intercellular adhesion molecule-1 gene and restenosis after coronary stenting in Chinese patients

Zhao Ping Liu, Yong Huo, Jian Ping Li, Yan Zhang, Lin Xue, Chun Yu Zhao, Xiu Mei Hong, Ai Qun Huang, Wei Gao

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Background. Inflammation is a major cause of restenosis after coronary stenting. Intercellular adhesion molecule-1 (ICAM-1) is an important adhesion molecule that plays a key role in the tight adhesion between leukocytes and vascular endothelium. The object of this study was to investigate the association between the K469E polymorphism of the ICAM-1 gene and restenosis after coronary stenting in North Chinese population. Methods. The ICAM-1 K469E polymorphism was genotyped using polymerase chain reaction-restriction fragment length polymorphism method in 124 patients who had undergone coronary stenting and coronary angiography at least 3 months earlier. Information on clinical risk factors and procedure-related data were also collected. Results. Of 124 enrolled patients in total, there were 72 cases of in-stent restenosis. The restenosis rate in this population was 58.1%. The frequencies of the three possible genotypes of the ICAM-1 K469E polymorphism were: KK genotype 50.8%, EE genotype 41.9%, and EK genotype 41.9%. Among restenosis patients, the frequency of the KK genotype was 58.3% and the frequency of E allele carriers was 41.7%. Among non-restenosis patients, the frequency of the KK genotype was 40.4%, and the frequency of E allele carriers was 59.6%. The distribution of these two genotype groups between restenosis and non-restenosis patients was significantly different (P = 0.049). Using multivariate logistic regression, the difference between the two groups was more apparent. The odds ratio of KK homozygotes vs E allele carriers was 2.6, with 95% confidence interval 1.2-5.8 (P = 0.018). After grading of risk factors, we found that the KK genotype was a stronger predictor of instent restenosis in obesity or hyperlipemia patients, with an odds ratio of 9.3 and 3.7, respectively (P <0.05). Conclusion. In our study population, KK homozygotes of the ICAM-1 codon 469 mutation had a higher risk of restenosis after coronary stenting, especially in the case of obese or hyperlipemia patients.

Original languageEnglish (US)
Pages (from-to)172-175
Number of pages4
JournalChinese medical journal
Volume117
Issue number2
StatePublished - Feb 2004
Externally publishedYes

Keywords

  • Coronary diseases
  • Gene polymorphism
  • Intercellular adhesion molecule-1
  • Restenosis
  • Stents

ASJC Scopus subject areas

  • General Medicine

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