Methylenetetrahydrofolate reductase gene polymorphism and its association with coronary artery disease

CONTEXT AND OBJECTIVE: Obstructive coronary artery disease (CAD) is characterized by the deposition of atherosclerotic plaque on the coronary artery wall. Its manifestations depend on interactions between environmental and genetic risk factors. The aim of this work was to analyze the frequency of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism in patients with CAD and its association with plasma homocysteine levels. Risk factors for CAD were also evaluated. DESIGN AND SETTING: Retrospective with blind quantitative analysis, at Hospital de Base, Faculdade de Medicina de São José do Rio Preto. METHODS: One hundred and twenty-seven individuals were studied. All completed a questionnaire to analyze risk factors for CAD. MTHFR polymorphism was investigated by restriction fragment length analysis and correlated with the number of affected arteries and degree of arterial obstruction determined by coronary cineangiography, and with plasma homocysteine levels measured by liquid chromatography/sequential mass spectrometry. RESULTS: Smoking (p = 0.02) and high-density lipoprotein cholesterol (p = 0.01) were associated with CAD. The C allele was the most prevalent in patients (0.61) and controls (0.66). There was no correlation between MTHFR/C677T polymorphism and plasma homocysteine levels. However, in patients with the TT genotype there was a correlation with the prevalence of coronary obstruction greater than 95% (p = 0.02) and the presence of two affected arteries (p = 0.04). CONCLUSIONS: The TT genotype is associated with coronary artery obstruction greater than 95% and the presence of two affected arteries. This confirms the relationship between genetic variants in specific patient subgroups and cardiovascular diseases.

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Main Authors: Guerzoni,Alexandre Rodrigues, Pavarino-Bertelli,Érika Cristina, Godoy,Moacir Fernandes de, Graça,Carla Renata, Biselli,Patrícia Matos, Souza,Dorotéia Rossi Silva, Bertollo,Eny Maria Goloni
Format: Digital revista
Language:English
Published: Associação Paulista de Medicina - APM 2007
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802007000100002
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spelling oai:scielo:S1516-318020070001000022007-05-02Methylenetetrahydrofolate reductase gene polymorphism and its association with coronary artery diseaseGuerzoni,Alexandre RodriguesPavarino-Bertelli,Érika CristinaGodoy,Moacir Fernandes deGraça,Carla RenataBiselli,Patrícia MatosSouza,Dorotéia Rossi SilvaBertollo,Eny Maria Goloni Coronary arteriosclerosis Atherosclerosis Methylenetetrahydrofolate reductase (NADPH2) Polymorphism genetic Homocysteine CONTEXT AND OBJECTIVE: Obstructive coronary artery disease (CAD) is characterized by the deposition of atherosclerotic plaque on the coronary artery wall. Its manifestations depend on interactions between environmental and genetic risk factors. The aim of this work was to analyze the frequency of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism in patients with CAD and its association with plasma homocysteine levels. Risk factors for CAD were also evaluated. DESIGN AND SETTING: Retrospective with blind quantitative analysis, at Hospital de Base, Faculdade de Medicina de São José do Rio Preto. METHODS: One hundred and twenty-seven individuals were studied. All completed a questionnaire to analyze risk factors for CAD. MTHFR polymorphism was investigated by restriction fragment length analysis and correlated with the number of affected arteries and degree of arterial obstruction determined by coronary cineangiography, and with plasma homocysteine levels measured by liquid chromatography/sequential mass spectrometry. RESULTS: Smoking (p = 0.02) and high-density lipoprotein cholesterol (p = 0.01) were associated with CAD. The C allele was the most prevalent in patients (0.61) and controls (0.66). There was no correlation between MTHFR/C677T polymorphism and plasma homocysteine levels. However, in patients with the TT genotype there was a correlation with the prevalence of coronary obstruction greater than 95% (p = 0.02) and the presence of two affected arteries (p = 0.04). CONCLUSIONS: The TT genotype is associated with coronary artery obstruction greater than 95% and the presence of two affected arteries. This confirms the relationship between genetic variants in specific patient subgroups and cardiovascular diseases.info:eu-repo/semantics/openAccessAssociação Paulista de Medicina - APMSao Paulo Medical Journal v.125 n.1 20072007-01-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802007000100002en10.1590/S1516-31802007000100002
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country Brasil
countrycode BR
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databasecode rev-scielo-br
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region America del Sur
libraryname SciELO
language English
format Digital
author Guerzoni,Alexandre Rodrigues
Pavarino-Bertelli,Érika Cristina
Godoy,Moacir Fernandes de
Graça,Carla Renata
Biselli,Patrícia Matos
Souza,Dorotéia Rossi Silva
Bertollo,Eny Maria Goloni
spellingShingle Guerzoni,Alexandre Rodrigues
Pavarino-Bertelli,Érika Cristina
Godoy,Moacir Fernandes de
Graça,Carla Renata
Biselli,Patrícia Matos
Souza,Dorotéia Rossi Silva
Bertollo,Eny Maria Goloni
Methylenetetrahydrofolate reductase gene polymorphism and its association with coronary artery disease
author_facet Guerzoni,Alexandre Rodrigues
Pavarino-Bertelli,Érika Cristina
Godoy,Moacir Fernandes de
Graça,Carla Renata
Biselli,Patrícia Matos
Souza,Dorotéia Rossi Silva
Bertollo,Eny Maria Goloni
author_sort Guerzoni,Alexandre Rodrigues
title Methylenetetrahydrofolate reductase gene polymorphism and its association with coronary artery disease
title_short Methylenetetrahydrofolate reductase gene polymorphism and its association with coronary artery disease
title_full Methylenetetrahydrofolate reductase gene polymorphism and its association with coronary artery disease
title_fullStr Methylenetetrahydrofolate reductase gene polymorphism and its association with coronary artery disease
title_full_unstemmed Methylenetetrahydrofolate reductase gene polymorphism and its association with coronary artery disease
title_sort methylenetetrahydrofolate reductase gene polymorphism and its association with coronary artery disease
description CONTEXT AND OBJECTIVE: Obstructive coronary artery disease (CAD) is characterized by the deposition of atherosclerotic plaque on the coronary artery wall. Its manifestations depend on interactions between environmental and genetic risk factors. The aim of this work was to analyze the frequency of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism in patients with CAD and its association with plasma homocysteine levels. Risk factors for CAD were also evaluated. DESIGN AND SETTING: Retrospective with blind quantitative analysis, at Hospital de Base, Faculdade de Medicina de São José do Rio Preto. METHODS: One hundred and twenty-seven individuals were studied. All completed a questionnaire to analyze risk factors for CAD. MTHFR polymorphism was investigated by restriction fragment length analysis and correlated with the number of affected arteries and degree of arterial obstruction determined by coronary cineangiography, and with plasma homocysteine levels measured by liquid chromatography/sequential mass spectrometry. RESULTS: Smoking (p = 0.02) and high-density lipoprotein cholesterol (p = 0.01) were associated with CAD. The C allele was the most prevalent in patients (0.61) and controls (0.66). There was no correlation between MTHFR/C677T polymorphism and plasma homocysteine levels. However, in patients with the TT genotype there was a correlation with the prevalence of coronary obstruction greater than 95% (p = 0.02) and the presence of two affected arteries (p = 0.04). CONCLUSIONS: The TT genotype is associated with coronary artery obstruction greater than 95% and the presence of two affected arteries. This confirms the relationship between genetic variants in specific patient subgroups and cardiovascular diseases.
publisher Associação Paulista de Medicina - APM
publishDate 2007
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802007000100002
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