期刊
BIOMED RESEARCH INTERNATIONAL
卷 2016, 期 -, 页码 -出版社
HINDAWI LTD
DOI: 10.1155/2016/1539671
关键词
-
资金
- Medical University of Silesia [KNW-1-014/N/4/0]
Purpose. Single nucleotide polymorphisms of the CYBA gene maymodify the risk of coronary artery disease (CAD). The aim of the present study was to investigate whether the *49A>G (rs7195830) polymorphism is associated with CAD. Materials and Methods. CYBA gene *49A>G polymorphism was determined in 481 subjects: 242 patients with premature CAD and 239 age and sex matched controls using the fluorescently labeled allele-specific oligonucleotidesmethod. Results. The frequency of the *49G allele carrier state was significantly higher in patients than in controls (84.8% versus 76.6%, resp., P = 0.020), as well as the frequency of the *49G allele (62.2% versus 54.0%, P = 0.009). Both factors were associated with CAD in the analyzed population (OR = 1.70, 95% CI: 1.04-2.76 for GG+AG versus AA and OR = 1.40, 95% CI: 1.08-1.83 for *49G versus *49A). Carrier state of the *49G allele was a stronger and independent risk factor for CAD among women (OR = 4.35, 95% CI: 1.50-13.20, P = 0.002), as well as the *49G allele (OR = 2.25, 95% CI: 1.34-3.77, P = 0.001). The *49G allele carrier state was also associated with left ventricular hypertrophy in patients with coronary artery disease (P = 0.015). Conclusion. The CYBA gene *49A>G polymorphism modifies the risk of coronary artery disease.
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