Association of Polymorphisms in Endothelial Nitric Oxide Synthesis and Renin-Angiotensin-Aldosterone System with Developing of Coronary Artery Disease in Bulgarian Patients

被引:17
|
作者
Mokretar, Katya [1 ]
Velinov, Hristo [1 ]
Postadzhiyan, Arman [2 ]
Apostolova, Margarita [1 ]
机构
[1] Bulgarian Acad Sci, Roumen Tzanev Inst Mol Biol, Med & Biol Res Lab, Acad G Bonchev St,Bl 21,Room 509, Sofia 1113, Bulgaria
[2] Univ Hosp St Anna, Clin Cardiol, Sofia, Bulgaria
关键词
II TYPE-1 RECEPTOR; SYNTHASE GENE POLYMORPHISMS; CONVERTING-ENZYME GENE; MYOCARDIAL-INFARCTION; HYPERTENSIVE PATIENTS; HEART-FAILURE; RENAL-DISEASE; RISK; METAANALYSIS; MORTALITY;
D O I
10.1089/gtmb.2015.0195
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aim: The purpose of this study was to evaluate the association of common polymorphisms in endothelial nitric oxide synthesis (eNOS; G894T) and renin-angiotensin-aldosterone system (angiotensin converting enzyme [ACE]I/D, angiotensinogenT704C, and angiotensin II receptor type 1A1166C) as risk factors in the pathogenesis of coronary artery disease (CAD) in Bulgarian patients. Methods: This study included 171 patients with CAD and 123 control subjects. Polymerase chain reaction-restriction fragment length polymorphism was used for studying the single-nucleotide polymorphisms. Statistical analysis was performed using statistical software PASW for Windows. Results: A significantly higher percentage of the eNOS T894 allele was found in patients with acute coronary syndrome (ACS), compared to controls (p=0.006) and patients with stable angina pectoris (SAP, p=0.005). Results from a binary regression analysis suggested that eNOS T allele and ACE D allele carriers were more likely to develop ACS than controls (T allele odds ratio [OR] 2.585, p=0.024; D allele OR 3.585, p=0.046) and patients with SAP (T allele OR 2.955, p=0.009; D allele OR 2.703, p=0.05). Exploratory evaluation of gene-gene combinations showed a significant association between eNOS-G894T/ACE-I/D and ACS compared to controls (p=0.022) and patients with SAP (p=0.017). Conclusions: The eNOS G894T and ACE I/D polymorphisms are associated with an increased risk of developing ACS after adjusting for classical risk factors for atherosclerosis in the Bulgarian cohort.
引用
收藏
页码:67 / 73
页数:7
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