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Single-nucleotide polymorphism of ADRβ2 and CDKN1B genes in Egyptian patients with coronary artery in-stent restenosis.
- Source :
-
Coronary artery disease [Coron Artery Dis] 2022 Jun 01; Vol. 33 (4), pp. 277-283. - Publication Year :
- 2022
-
Abstract
- Background: In-stent restenosis is a common complication after percutaneous coronary intervention. The purpose of the current study is to look for associations of genetic variation in adrenergic beta-2 receptor (ADRβ2), and cyclin-dependent kinase inhibitor 1B (CDKN1B) genes in patients diagnosed with in-stent restenosis (ISR) after percutaneous coronary intervention in the Egyptians.<br />Methods: Polymorphisms in ADRβ2 and CDKN1B were determined using PCR-restriction fragment length polymorphism in 200 Egyptian patients who underwent coronary angioplasty and stent placement of whom 100 patients developed ISR.<br />Results: We found that the GG genotype of ADRβ2 and CC genotype of CDKN1B were more likely to develop restenosis after stenting (odds ratio = 3.7 and 3.2; P = 0.001, respectively). Our study considered that male sex, diabetes, obesity, bare-metal stents type of implanted stents, longer stents, GG genotype of ADRβ2, and CC genotype of CDK1B were significant independent predictors for ISR.<br />Conclusion: our results indicate that ADRβ2 (rs1042713) and CDKN1B (rs36228499) could be associated with the development of ISR in Egyptians.<br /> (Copyright © 2022 Wolters Kluwer Health, Inc. All rights reserved.)
- Subjects :
- Humans
Male
Constriction, Pathologic complications
Coronary Angiography adverse effects
Coronary Vessels
Cyclin-Dependent Kinase Inhibitor p27 genetics
Egypt
Polymorphism, Single Nucleotide
Receptors, Adrenergic, beta genetics
Risk Factors
Stents adverse effects
Coronary Restenosis etiology
Subjects
Details
- Language :
- English
- ISSN :
- 1473-5830
- Volume :
- 33
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Coronary artery disease
- Publication Type :
- Academic Journal
- Accession number :
- 35044333
- Full Text :
- https://doi.org/10.1097/MCA.0000000000001123