Literature DB >> 14975197

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

Zhao-ping Liu1, Yong Huo, Jian-ping Li, Yan Zhang, Lin Xue, Chun-yu Zhao, Xiu-mei Hong, Ai-qun Huang, Wei Gao.   

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 in-stent 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.

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Year:  2004        PMID: 14975197

Source DB:  PubMed          Journal:  Chin Med J (Engl)        ISSN: 0366-6999            Impact factor:   2.628


  4 in total

1.  Polymorphisms in the ICAM1 gene predict circulating soluble intercellular adhesion molecule-1(sICAM-1).

Authors:  Suzette J Bielinski; Alex P Reiner; Deborah Nickerson; Chris Carlson; Kent R Bailey; Bharat Thyagarajan; Leslie A Lange; Eric A Boerwinkle; David R Jacobs; Myron D Gross
Journal:  Atherosclerosis       Date:  2011-02-18       Impact factor: 5.162

2.  K469E polymorphism of the intercellular adhesion molecule-1 gene in Egyptians with coronary heart disease.

Authors:  Amal A Mohamed; Laila Rashed; Hoda Amin; Manal Abu-Farha; Soheir Abu El Fadl; Sameh Pakhoum
Journal:  Ann Saudi Med       Date:  2010 Nov-Dec       Impact factor: 1.526

3.  Intercellular adhesion molecule-1 gene K469E polymorphism and ischemic stroke: a case-control study in a Chinese population.

Authors:  Xiao Xia Li; Jian Ping Liu; Jin Quan Cheng; Sheng Hong Han; Yi Jie Geng; Sheng Wei; Shi Tong Gao; Da Na Huang; Shao Fa Nie
Journal:  Mol Biol Rep       Date:  2008-09-14       Impact factor: 2.316

Review 4.  Genetics of coronary artery disease and myocardial infarction.

Authors:  Xuming Dai; Szymon Wiernek; James P Evans; Marschall S Runge
Journal:  World J Cardiol       Date:  2016-01-26
  4 in total

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