Polymorphisms of the methylenetetrahydrofolate reductase, vascular endothelial growth factor, endothelial nitric oxide synthase, monocyte chemoattractant protein-1 and apolipoprotein E genes are not associated with carotid intima-media thickness
dc.contributor.author | Alioglu E. | |
dc.contributor.author | Turk U. | |
dc.contributor.author | Cam S. | |
dc.contributor.author | Abbasaliyev A. | |
dc.contributor.author | Tengiz I. | |
dc.contributor.author | Ercan E. | |
dc.date.accessioned | 2024-07-22T08:22:04Z | |
dc.date.available | 2024-07-22T08:22:04Z | |
dc.date.issued | 2009 | |
dc.description.abstract | Background: Single nucleotide polymorphisms in the 5,10-methyl-enetetrahydrofolate reductase (MTHFR), vascular endothelial growth factor (VEGF), endothelial nitric oxide synthase (eNOS), monocyte chemoattractant protein-1 (MCP-1) and apolipoprotein E (ApoE) genes appear to be a genetic risk factor for atherosclerosis. Common carotid intima-media thickness (cIMT) provides information on the severity of atherosclerosis. Objective: To investigate the relationship between cIMT and gene polymorphisms associated with atherosclerosis in Turkish patients with coronary artery disease (CAD). Methods: Sixty-two patients with angiographically diagnosed stable CAD were divided into two groups according to their cIMT values (group 1: n=35, cIMT of 1 mm or greater; group 2: n=27, cIMT of less than 1 mm). MTHFR 677 C/T, VEGF -460 C/T, eNOS 894 G/T, MCP-1 -2518 A/G and ApoE (E2, E3 and E4) gene polymorphisms (where A is adenine, C is cytosine, G is guanine and T is thymine) were analyzed by polymerase chain reaction and restriction fragment length polymorphism. Evaluations of cardiovascular risk factors and coronary atherosclerotic lesions were performed in all patients. Serum homocysteine and high-sensitivity C-reactive protein were measured and compared between the two groups. Results: Serum high-sensitivity C-reactive protein (P=0.04) and homocysteine (P=0.006) levels were higher in group 1 than in group 2. The ratio of multivessel CAD and previous myocardial infarction was significantly higher in group 1 than in group 2 (P=0.014). In the study population, no significant difference in cIMT was observed according to the polymorphisms studied. Only hyperhomocysteinemia (OR 1.17 [95% CI 1.01 to 1.35], P=0.033) and previous myocardial infarction (OR 3.76 [95% CI 1.10 to 12.81], P=0.034) maintained a significant correlation with cIMT on multiple logistic regression analysis. Conclusion: cIMT is increased in patients with hyperhomocysteinemia, inflammation and extended CAD. MTHFR 677 C/T, VEGF -460 C/T, eNOS 894 G/ T, MCP-1 -2518 A/G and ApoE single nucleotide polymorphisms were not associated with increased cIMT. © 2009 Pulsus Group Inc. All rights reserved. | |
dc.identifier.DOI-ID | 10.1016/S0828-282X(09)70022-4 | |
dc.identifier.issn | 0828282X | |
dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/18909 | |
dc.language.iso | English | |
dc.publisher | Pulsus Group Inc. | |
dc.rights | All Open Access; Green Open Access | |
dc.subject | 5,10 methylenetetrahydrofolate reductase (FADH2) | |
dc.subject | apolipoprotein E | |
dc.subject | C reactive protein | |
dc.subject | endothelial nitric oxide synthase | |
dc.subject | homocysteine | |
dc.subject | monocyte chemotactic protein 1 | |
dc.subject | vasculotropin | |
dc.subject | adult | |
dc.subject | amino acid blood level | |
dc.subject | artery intima proliferation | |
dc.subject | article | |
dc.subject | cardiovascular risk | |
dc.subject | coronary artery atherosclerosis | |
dc.subject | coronary artery disease | |
dc.subject | DNA polymorphism | |
dc.subject | female | |
dc.subject | genetic association | |
dc.subject | genotype | |
dc.subject | heart infarction | |
dc.subject | human | |
dc.subject | major clinical study | |
dc.subject | male | |
dc.subject | polymerase chain reaction | |
dc.subject | protein blood level | |
dc.subject | restriction fragment length polymorphism | |
dc.subject | risk assessment | |
dc.subject | single nucleotide polymorphism | |
dc.subject | Turkey (republic) | |
dc.title | Polymorphisms of the methylenetetrahydrofolate reductase, vascular endothelial growth factor, endothelial nitric oxide synthase, monocyte chemoattractant protein-1 and apolipoprotein E genes are not associated with carotid intima-media thickness | |
dc.type | Article |