Methylene tetrahydrofolate reductase (MTHFR) and nitric oxide synthase (ecNOS) genes and risks of peripheral arterial disease and coronary heart disease: Edinburgh artery study

• Published in: Atherosclerosis Vol. 150; no. 1; pp. 179 - 185
• Main Authors: Fowkes, F.G.R, Lee, A.J, Hau, C.M, Cooke, A, Connor, J.M, Lowe, G.D.O
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier Ireland Ltd 01.05.2000; Elsevier
• Subjects: Aged; Alleles; Arteriosclerosis - genetics; Atherosclerosis (general aspects, experimental research); Biological and medical sciences; Blood and lymphatic vessels; Cardiology. Vascular system; Coronary Disease - genetics; Coronary heart disease; Female; Gene Frequency; Genes; Genotype; Homocysteine; Humans; Male; Medical sciences; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Nitric oxide; Nitric Oxide Synthase - genetics; Nitric Oxide Synthase Type III; Oxidoreductases Acting on CH-NH Group Donors - genetics; Peripheral arterial disease; Peripheral Vascular Diseases - genetics; Risk Factors; Peripheral arterial disease; Homocysteine; Coronary heart disease; Genes; Nitric oxide; Human; Methylenetetrahydrofolate reductase (NADPH); Thiol; Enzyme; Pathogenesis; Genetic variant; Cardiovascular disease; Exploration; Genotype; Biosynthesis; Synthase; Metabolism; Genetic determinism; Vascular disease; Sulfur containing aminoacid; Phenotype; Gene; Atherosclerosis; Risk factor; Oxidoreductases
• ISSN: 0021-9150; 1879-1484
• DOI: 10.1016/S0021-9150(99)00366-4

Hyperhomocysteinaemia and reduced nitric oxide synthesis may each result in endothelial dysfunction predisposing to atherogenesis. Genetic variants of methylene tetrahydrofolate reductase (MTHFR) and endothelial nitric oxide synthase (ecNOS) influence homocysteine metabolism and nitric oxide synthesis, respectively and might thus be determinants of the risk of atherosclerotic disease. The aim of our study was to identify, in a general population sample, the risks of peripheral arterial disease and of coronary heart disease related to MTHFR (175;198) and ecNOS (4;5) polymorphisms. In the Edinburgh Artery Study, which is a population based cohort study, 940 men and women aged 60–79 years, who had previously been selected at random from the general population, had DNA extracted from a venous blood sample. Based on a clinical examination at baseline and follow up investigations, three groups of subjects were identified: those with peripheral arterial disease ( n=80), those with coronary heart disease ( n=137), and healthy controls who had no evidence of cardiovascular disease ( n=300). The distributions of the ecNOS and MTHFR genotypes did not differ significantly between the groups with and without cardiovascular disease. However, the ecNOS-4 allele (frequency 0.13) was related to the occurrence of coronary heart disease in non smokers, OR=2.47 (95% CI [1.42, 4.34], P=0.02). No association was found with peripheral arterial disease. The MTHFR-175 allele (frequency 0.31) was not related to coronary heart disease, but was associated with a reduced risk of peripheral arterial disease, OR=0.54 (95% CI [0.32, 0.90], P=0.02). Neither the ecNOS-4 allele or MTHFR-175 allele was related to the ankle brachial pressure index in the whole study population. In conclusion, the ecNOS-4 allele was associated with a slightly increased risk of coronary heart disease in non-smokers, but otherwise the MTHFR and ecNOS genotypes appeared to have little influence on the risks of peripheral arterial disease and coronary heart disease in this older population.