RETRACTED: Association between T-786C polymorphism of endothelial nitric oxide synthase gene and level of the vessel dilation factor in patients with coronary artery disease (Retracted article. See vol. 8, pg. 51, 2019)
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作者:
Khaki-Khatibi, Fatemeh
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Tabriz Univ Med Sci, Fac Med, Dept Clin Biochem, Tabriz, IranTabriz Univ Med Sci, Fac Med, Dept Clin Biochem, Tabriz, Iran
Khaki-Khatibi, Fatemeh
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Yaghoubi, Ali Reza
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机构:Tabriz Univ Med Sci, Fac Med, Dept Clin Biochem, Tabriz, Iran
Yaghoubi, Ali Reza
Ghojazadeh, Morteza
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机构:Tabriz Univ Med Sci, Fac Med, Dept Clin Biochem, Tabriz, Iran
Ghojazadeh, Morteza
Rahbani-Nobar, Mohammad
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机构:Tabriz Univ Med Sci, Fac Med, Dept Clin Biochem, Tabriz, Iran
Rahbani-Nobar, Mohammad
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[1] Tabriz Univ Med Sci, Fac Med, Dept Clin Biochem, Tabriz, Iran
Various polymorphisms on endothelial nitric oxide synthase (eNOs) gene cause reduced production of NO, the endothelial relaxing factor, and may accelerate the process of atherosclerosis. The study designed to investigate the frequency of T-786C polymorphism of the eNOs gene in patients suffering from coronary artery disease (CAD) in north-west of Iran. One hundred twenty subjects including 60 patients with angiographically diagnosed CAD and 60 age and sex matched CAD-free subjects as control were studied. The levels of nitric oxide in the samples were measured with the Griess Method. The genotype studies were carried using allele specific PCR. Comparing with the control, reduced levels of NO were noticed in the patient group (P<0.05). Statistical analysis showed that the genotype TC associated with risk of CAD (OR=2.50, 95% CI: 1.13-5.50, P=0.023). The prevalence of C allele was significantly higher in patients compared to control group (OR=2.04, 95% CI: 1.16-3.57, P=0.013). The low levels of NO and increased frequency of T-786C polymorphism might be a risk factor in progression of coronary artery disease in the studied subjects.
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China Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R China
Liaoning Canc Hosp & Inst, Dept Radiat Oncol, Liaoning, Peoples R ChinaChina Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R China
Qu, Yan-Li
Yu, Hong
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Liaoning Canc Hosp & Inst, Dept Radiat Oncol, Liaoning, Peoples R ChinaChina Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R China
Yu, Hong
Chen, Yan-Zhi
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China Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R ChinaChina Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R China
Chen, Yan-Zhi
Zhao, Yu-Xia
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China Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R ChinaChina Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R China
Zhao, Yu-Xia
Chen, Guang-Jun
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Clin Border Control Bur Liaoning Prov, Liaoning, Peoples R ChinaChina Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R China
Chen, Guang-Jun
Bai, Lu
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China Med Univ, Affiliated Hosp 1, Dept Radiat Oncol, Shenyang, Peoples R ChinaChina Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R China
Bai, Lu
Liu, Dan
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China Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R ChinaChina Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R China
Liu, Dan
Su, Hong-Xin
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China Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R ChinaChina Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R China
Su, Hong-Xin
Wang, He-Tong
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China Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R ChinaChina Med Univ, Affiliated Hosp 4, Dept Radiat Oncol, Shenyang 110032, Peoples R China