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https://www.um.edu.mt/library/oar/handle/123456789/48714| Title: | CYP2C19*2 allele carrier status and coronary in-stent restenosis : is there an association? |
| Authors: | Wirth, Francesca Zahra, Graziella Xuereb, Robert G. Barbara, Christopher H. Camilleri, Liberato Fenech, Albert Azzopardi, Lilian M. |
| Keywords: | Clopidogrel Coronary arteries -- Stenosis Chromosome polymorphism Pharmacogenetics |
| Issue Date: | 2018 |
| Publisher: | Medwell Journals |
| Citation: | Wirth, F., Zahra, G., Xuereb, R. G., Barbara, C., Camilleri, L., Fenech, A., & Azzopardi, L. M. (2018). CYP2C19*2 allele carrier status and coronary in-stent restenosis : is there an association?. Journal of Exploratory Research in Pharmacology, 3(2), 55-60. |
| Abstract: | Background and objective: The CYP2C19*2 allele is associated with reduced clopidogrel bioactivation, increasing the risk of complications after percutaneous coronary intervention (PCI), particularly stent thrombosis. Recently published data suggests that CYP2C19*2 allele carriers have a higher risk for in-stent restenosis (ISR) after endovascular treatment. Very few studies have investigated the relationship between CYP2C19*2 and coronary ISR, with no significant association reported. The objective of this study was to assess the relationship between CYP2C19*2 allele carrier status and coronary ISR. Methods: Patients with previous PCI with stenting and who were scheduled for elective PCI after coronary angiogram were recruited from the cardiac catheterization suite over a 12-month period. The angiography report of each patient was perused to identify patients requiring PCI due to ISR. For patients with angiography-confirmed ISR, date of previous PCI to the restenosed stent was noted. CYP2C19*2 genotyping was undertaken using a TaqMan® Drug Metabolism assay. The association between CYP2C19*2 allele carrier status and incidence of coronary ISR within 1 year was assessed using Fisher’s exact test (p < 0.05 significance) and by calculating the odds ratio (OR) with a 95% confidence interval (CI). Results: Of the 82 patients with previous PCI, 29 (35.4%) had angiography-confirmed ISR (12 carriers, 17 noncarriers of CYP2C19*2). In 13 (44.8%) of these patients, the restenosed stent was deployed within 1 year and the patients were on clopidogrel therapy at the time of repeat PCI (8 carriers, 5 non-carriers of CYP2C19*2). The association between CYP2C19*2 allele carrier status and ISR within 1 year was not statistically significant (Fisher’s exact p = 0.067; OR: 4.80, 95% CI: 0.98–23.54, p = 0.053). Conclusions: Despite a higher proportion of CYP2C19*2 allele carriers exhibiting ISR within 1 year compared to non-carriers, the association was not statistically significant. This result may be attributed to the small sample size, and larger prospective studies are recommended to further assess this association. |
| URI: | https://www.um.edu.mt/library/oar/handle/123456789/48714 |
| Appears in Collections: | Scholarly Works - FacM&SPha Scholarly Works - FacSciSOR |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| CYP2C19_2_allele_carrier_status_and_coronary_in_stent_restenosis.pdf | 715.69 kB | Adobe PDF | View/Open |
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