Association of polymorphisms of renin angiotensin system and endothelial nitric oxide synthase genes with premature cardiovascular disease in an Iranian population

被引:3
|
作者
Poorzand, Hoorak [1 ]
Fazeli, Bahareh [2 ]
Khajavi, Omid [3 ]
Gholoobi, Arash [3 ]
Keihanian, Faeze [3 ,5 ]
Morovatdar, Negar [4 ]
机构
[1] Mashhad Univ Med Sci, Vasc & Endovasc Surg Res Ctr, Mashhad, Iran
[2] Mashhad Univ Med Sci, Inflammat & Inflammatory Dis Res Ctr, Mashhad, Iran
[3] Mashhad Univ Med Sci, Fac Med, Cardiovasc Dept, Mashhad, Iran
[4] Mashhad Univ Med Sci, Fac Med, Clin Res Unit, Mashhad, Iran
[5] Mashhad Univ Med Sci, Pharmaceut Res Ctr, Mashhad, Iran
关键词
Polymorphism; Renin angiotensin; Endothelial nitric oxide synthase; Premature cardiovascular disease; CORONARY-ARTERY-DISEASE; CONVERTING-ENZYME GENE; RISK-FACTORS; INSERTION/DELETION POLYMORPHISM; ENOS GLU298ASP; VARIANTS; G894T;
D O I
10.1186/s12872-023-03276-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionThe study of polymorphisms and their relationship with diseases is very important for risk assessment. The aim of this study was to determine the relationship between early risk of coronary artery disease(CAD) with renin-angiotensin(RAS) genes and endothelial nitric oxide synthase(eNOS) in a sample of the Iranian population.Methods & materialsIn this cross-sectional study, 63 patients with premature CAD and 72 healthy samples were enrolled. Polymorphism of the promotor region of eNOS- and ACE-I/D (Angiotensin Converting Enzyme-I/D) polymorphism was evaluated. Polymerase chain reaction (PCR) test and PCR-RFLP (Restriction Fragment Length Polymorphism) was performed for ACE and eNOS-786 gene, respectively.ResultsThe frequency of deletion(D) for the ACE gene was significantly higher in patients(96% versus 61%; P < 0.001). Conversely, the number of defective C alleles for the eNOS gene was similar in both groups (p > 0.9).ConclusionACE polymorphism seems to be an independent risk factor for premature CAD.
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页数:6
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