Avaliação da relação entre o polimorfismo C677T no gene para MTHFR e a concentração plasmática de homocisteína na doença arterial coronariana

Detalhes bibliográficos
Autor(a) principal: Muniz, Maria Tereza C.
Data de Publicação: 2006
Outros Autores: Siqueira, Erika R.f., Fonseca, Rosana A., D'Almeida, Vânia [UNIFESP], Hotta, Júlia K., Santos, José E. dos, Cavalcanti, Maria do Socorro de Mendonça, Sampaio, Cláudio A.m.
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
dARK ID: ark:/48912/001300000xvkj
Texto Completo: http://dx.doi.org/10.1590/S0004-27302006000600012
http://repositorio.unifesp.br/handle/11600/3405
Resumo: OBJECTIVE: The aim of this study is to determine the prevalence of C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism and correlate it with plasma homocysteine levels in coronary artery disease (CAD). METHODS: Ninety-three patients with documented CAD from Hospital Universitário Oswaldo Cruz (Recife, PE, Brazil) and 108 healthy controls were evaluated. Homocysteine and folate levels were determined by HPLC and chemoluminescence, respectively, and lipid profile was considered. Genotyping was done by RFLP/PCR. RESULTS: The groups were homogeneous for the C677T polymorphisms. The homocysteine level in cases (11.7 µmol/L) was statistically different from that observed in controls (8.84 µmol/L, p< 0.05). It was also observed that 72% of the patients had homocysteine values above12 µmol/L while the control group presented only 32% in this range. There was no relationship between homozigosity for the C677T polymorphism and the homocysteine level (p= 0.634). We noticed statistical differences between folate levels from patients and controls (6.22 and 7.69 ng/dL, p< 0.05, respectively). However, there was no correlation between homocysteine and folate concentrations in the entire group (r= -0.202). Comparing cases and controls, the odds ratio (OR) when homocysteine is high and folate is low was OR= 11.9; CI 95%= 4.16-34.42, p< 0.01. CONCLUSION: A lack of correlation between C677T mutation and homocysteine level suggests that environmental factors and others genetic factors seem to exert more influence on homocysteine level in this population.
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spelling Avaliação da relação entre o polimorfismo C677T no gene para MTHFR e a concentração plasmática de homocisteína na doença arterial coronarianaEvaluation of MTHFR C677T gene polymorphism and homocysteine level in coronary atherosclerotic diseaseCoronary arterial diseaseHomocysteineMethylenetetraidrofolate reductaseFolatePolymorphismDislipidemiasDoença aterosclerótica coronarianaHomocisteínaMetilenotetraidrofolato redutaseFolatoPolimorfismoDislipidemiasOBJECTIVE: The aim of this study is to determine the prevalence of C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism and correlate it with plasma homocysteine levels in coronary artery disease (CAD). METHODS: Ninety-three patients with documented CAD from Hospital Universitário Oswaldo Cruz (Recife, PE, Brazil) and 108 healthy controls were evaluated. Homocysteine and folate levels were determined by HPLC and chemoluminescence, respectively, and lipid profile was considered. Genotyping was done by RFLP/PCR. RESULTS: The groups were homogeneous for the C677T polymorphisms. The homocysteine level in cases (11.7 µmol/L) was statistically different from that observed in controls (8.84 µmol/L, p< 0.05). It was also observed that 72% of the patients had homocysteine values above12 µmol/L while the control group presented only 32% in this range. There was no relationship between homozigosity for the C677T polymorphism and the homocysteine level (p= 0.634). We noticed statistical differences between folate levels from patients and controls (6.22 and 7.69 ng/dL, p< 0.05, respectively). However, there was no correlation between homocysteine and folate concentrations in the entire group (r= -0.202). Comparing cases and controls, the odds ratio (OR) when homocysteine is high and folate is low was OR= 11.9; CI 95%= 4.16-34.42, p< 0.01. CONCLUSION: A lack of correlation between C677T mutation and homocysteine level suggests that environmental factors and others genetic factors seem to exert more influence on homocysteine level in this population.OBJETIVO: O objetivo deste trabalho é determinar a prevalência do polimorfismo C677T do gene metilenotetraidrofolato redutase (MTHFR) e associá-la com a concentração plasmática de homocisteína plasmática na doença arterial coronariana (DAC). MÉTODOS: Foram avaliados 93 pacientes com DAC documentada, atendidos no Hospital Universitário Oswaldo Cruz (Recife, PE, Brasil), e 108 controles sem a doença. Foram determinados os perfis lipídicos de pacientes e controles. As concentrações plasmáticas de homocisteína e folato foram determinadas por HPLC e quimioluminescência, respectivamente. A genotipagem foi realizada por RFLP/PCR. RESULTADOS: Os grupos de pacientes e controles foram homogêneos quanto aos perfis genéticos do polimorfismo investigado. Nos pacientes, as concentrações plasmáticas médias de homocisteina (11,7 ± 4,4 µmol/L) e de folato (6,22 ± 3,0 ng/dL) foram estatisticamente diferentes daquelas observadas nos controles (8,84 ± 3,2 µmol/L e 7,69 ± 3,1 ng/dL, respectivamente), ao nível de significância de 0,05. Entretanto, não houve correlação entre concentração plasmática de homocisteína e folato nos pacientes (r= -0,202). Não foi observada associação entre a homozigosidade 677TT para MTHFR e a concentração plasmática de homocisteína sérica (p= 0,634). A comparação dos casos e controles que apresentaram simultaneamente alta concentração plasmática de homocisteína e baixa concentração de folato, resultou numa razão de chance superior à de cada variável analisada independentemente (RC= 11,9; IC 95%= 4,16-34,42, p< 0,01). CONCLUSÕES: A mutação C677T não parece ser um fator genético importante capaz de explicar a hiperhomocisteinemia moderada observada nos pacientes com DAC. Outros fatores, ambientais e genéticos, devem ser investigados.Universidade Federal de São Paulo (UNIFESP) Departamento de Pediatria Laboratório de Erros Inatos de MetabolismoUniversidade de Pernambuco ICB Departamento de Ciências FisiológicasUniversidade de São Paulo Faculdade de Medicina de Ribeirão Preto Hospital das ClínicasUNIFESP, Depto. de Pediatria Laboratório de Erros Inatos de MetabolismoSciELOFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Sociedade Brasileira de Endocrinologia e MetabologiaUniversidade Federal de São Paulo (UNIFESP)Universidade de Pernambuco ICB Departamento de Ciências FisiológicasUniversidade de São Paulo (USP)Muniz, Maria Tereza C.Siqueira, Erika R.f.Fonseca, Rosana A.D'Almeida, Vânia [UNIFESP]Hotta, Júlia K.Santos, José E. dosCavalcanti, Maria do Socorro de MendonçaSampaio, Cláudio A.m.2015-06-14T13:36:35Z2015-06-14T13:36:35Z2006-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1059-1065application/pdfhttp://dx.doi.org/10.1590/S0004-27302006000600012Arquivos Brasileiros de Endocrinologia & Metabologia. Sociedade Brasileira de Endocrinologia e Metabologia, v. 50, n. 6, p. 1059-1065, 2006.10.1590/S0004-27302006000600012S0004-27302006000600012.pdf0004-2730S0004-27302006000600012http://repositorio.unifesp.br/handle/11600/3405ark:/48912/001300000xvkjporArquivos Brasileiros de Endocrinologia & Metabologiainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-05T14:53:53Zoai:repositorio.unifesp.br/:11600/3405Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T20:44:12.677501Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Avaliação da relação entre o polimorfismo C677T no gene para MTHFR e a concentração plasmática de homocisteína na doença arterial coronariana
Evaluation of MTHFR C677T gene polymorphism and homocysteine level in coronary atherosclerotic disease
title Avaliação da relação entre o polimorfismo C677T no gene para MTHFR e a concentração plasmática de homocisteína na doença arterial coronariana
spellingShingle Avaliação da relação entre o polimorfismo C677T no gene para MTHFR e a concentração plasmática de homocisteína na doença arterial coronariana
Muniz, Maria Tereza C.
Coronary arterial disease
Homocysteine
Methylenetetraidrofolate reductase
Folate
Polymorphism
Dislipidemias
Doença aterosclerótica coronariana
Homocisteína
Metilenotetraidrofolato redutase
Folato
Polimorfismo
Dislipidemias
title_short Avaliação da relação entre o polimorfismo C677T no gene para MTHFR e a concentração plasmática de homocisteína na doença arterial coronariana
title_full Avaliação da relação entre o polimorfismo C677T no gene para MTHFR e a concentração plasmática de homocisteína na doença arterial coronariana
title_fullStr Avaliação da relação entre o polimorfismo C677T no gene para MTHFR e a concentração plasmática de homocisteína na doença arterial coronariana
title_full_unstemmed Avaliação da relação entre o polimorfismo C677T no gene para MTHFR e a concentração plasmática de homocisteína na doença arterial coronariana
title_sort Avaliação da relação entre o polimorfismo C677T no gene para MTHFR e a concentração plasmática de homocisteína na doença arterial coronariana
author Muniz, Maria Tereza C.
author_facet Muniz, Maria Tereza C.
Siqueira, Erika R.f.
Fonseca, Rosana A.
D'Almeida, Vânia [UNIFESP]
Hotta, Júlia K.
Santos, José E. dos
Cavalcanti, Maria do Socorro de Mendonça
Sampaio, Cláudio A.m.
author_role author
author2 Siqueira, Erika R.f.
Fonseca, Rosana A.
D'Almeida, Vânia [UNIFESP]
Hotta, Júlia K.
Santos, José E. dos
Cavalcanti, Maria do Socorro de Mendonça
Sampaio, Cláudio A.m.
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Universidade de Pernambuco ICB Departamento de Ciências Fisiológicas
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Muniz, Maria Tereza C.
Siqueira, Erika R.f.
Fonseca, Rosana A.
D'Almeida, Vânia [UNIFESP]
Hotta, Júlia K.
Santos, José E. dos
Cavalcanti, Maria do Socorro de Mendonça
Sampaio, Cláudio A.m.
dc.subject.por.fl_str_mv Coronary arterial disease
Homocysteine
Methylenetetraidrofolate reductase
Folate
Polymorphism
Dislipidemias
Doença aterosclerótica coronariana
Homocisteína
Metilenotetraidrofolato redutase
Folato
Polimorfismo
Dislipidemias
topic Coronary arterial disease
Homocysteine
Methylenetetraidrofolate reductase
Folate
Polymorphism
Dislipidemias
Doença aterosclerótica coronariana
Homocisteína
Metilenotetraidrofolato redutase
Folato
Polimorfismo
Dislipidemias
description OBJECTIVE: The aim of this study is to determine the prevalence of C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism and correlate it with plasma homocysteine levels in coronary artery disease (CAD). METHODS: Ninety-three patients with documented CAD from Hospital Universitário Oswaldo Cruz (Recife, PE, Brazil) and 108 healthy controls were evaluated. Homocysteine and folate levels were determined by HPLC and chemoluminescence, respectively, and lipid profile was considered. Genotyping was done by RFLP/PCR. RESULTS: The groups were homogeneous for the C677T polymorphisms. The homocysteine level in cases (11.7 µmol/L) was statistically different from that observed in controls (8.84 µmol/L, p< 0.05). It was also observed that 72% of the patients had homocysteine values above12 µmol/L while the control group presented only 32% in this range. There was no relationship between homozigosity for the C677T polymorphism and the homocysteine level (p= 0.634). We noticed statistical differences between folate levels from patients and controls (6.22 and 7.69 ng/dL, p< 0.05, respectively). However, there was no correlation between homocysteine and folate concentrations in the entire group (r= -0.202). Comparing cases and controls, the odds ratio (OR) when homocysteine is high and folate is low was OR= 11.9; CI 95%= 4.16-34.42, p< 0.01. CONCLUSION: A lack of correlation between C677T mutation and homocysteine level suggests that environmental factors and others genetic factors seem to exert more influence on homocysteine level in this population.
publishDate 2006
dc.date.none.fl_str_mv 2006-12-01
2015-06-14T13:36:35Z
2015-06-14T13:36:35Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0004-27302006000600012
Arquivos Brasileiros de Endocrinologia & Metabologia. Sociedade Brasileira de Endocrinologia e Metabologia, v. 50, n. 6, p. 1059-1065, 2006.
10.1590/S0004-27302006000600012
S0004-27302006000600012.pdf
0004-2730
S0004-27302006000600012
http://repositorio.unifesp.br/handle/11600/3405
dc.identifier.dark.fl_str_mv ark:/48912/001300000xvkj
url http://dx.doi.org/10.1590/S0004-27302006000600012
http://repositorio.unifesp.br/handle/11600/3405
identifier_str_mv Arquivos Brasileiros de Endocrinologia & Metabologia. Sociedade Brasileira de Endocrinologia e Metabologia, v. 50, n. 6, p. 1059-1065, 2006.
10.1590/S0004-27302006000600012
S0004-27302006000600012.pdf
0004-2730
S0004-27302006000600012
ark:/48912/001300000xvkj
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Arquivos Brasileiros de Endocrinologia & Metabologia
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1059-1065
application/pdf
dc.publisher.none.fl_str_mv Sociedade Brasileira de Endocrinologia e Metabologia
publisher.none.fl_str_mv Sociedade Brasileira de Endocrinologia e Metabologia
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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