Genetic polymorphisms involved in folate metabolism and concentrations of methylmalonic acid and folate on plasma homocysteine and risk of coronary artery disease


Autoria(s): BISELLI, Patricia Matos; GUERZONI, Alexandre Rodrigues; GODOY, Moacir Fernandes de; EBERLIN, Marcos Nogueira; HADDAD, Renato; CARVALHO, Valdemir Melechco; VANNUCCHI, Helio; PAVARINO-BERTELLI, Erika Cristina; GOLONI-BERTOLLO, Eny Maria
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

Objectives Alterations in the enzymes involved in homocysteine (Hcy) metabolism or vitamin deficiency could play a role in coronary artery disease (CAD) development. This study investigated the influence of MTHFR and MTR gene polymorphisms, plasma folate and MMA on Hcy concentrations and CAD development. MMA and folate concentrations were also investigated according to the polymorphisms. Methods Two hundred and eighty-three unrelated Caucasian individuals undergoing coronary angiography (175 with CAD and 108 non-CAD) were assessed in a case-control study. Plasma Hcy and MMA were measured by liquid chromatography/tandem mass spectrometry. Plasma folate was measured by competitive immunoassay. Dietary intake was evaluated using a nutritional questionnaire. Polymorphisms MTHFR and MTR were investigated by polymerase chain reaction (PCR) followed by enzyme digestion or allele-specific PCR. Results Hcy mean concentrations were higher in CAD patients compared to controls, but below statistical significance (P = 0.246). Increased MMA mean concentrations were frequently observed in the CAD group (P = 0.048). Individuals with MMA concentrations > 0.5 mu mol/l (vitamin B(12) deficiency) were found only in the CAD group (P = 0.004). A positive correlation between MMA and Hcy mean concentrations was observed in both groups, CAD (P = 0.001) and non-CAD (P = 0.020). MMA mean concentrations were significantly higher in patients with hyperhomocysteinemia in both groups, CAD and non-CAD (P = 0.0063 and P = 0.013, respectively). Folate mean concentration was significantly lower in carriers of the wild-type MTHFR 1298AA genotype (P = 0.010). Conclusion Our results suggest a correlation between the MTHFR A1298C polymorphism and plasma folate concentration. Vitamin B(12) deficiency, reflected by increased MMA concentration, is an important risk factor for the development both of hyperhomocysteinemia and CAD.

State of Sao Paulo Research Foundation (FAPESP)

Coordination for the Improvement of Higher Education (CAPES)

National Council for Scientific and Technological Development (CNPq)

Fleury Medicine and Health

Identificador

JOURNAL OF THROMBOSIS AND THROMBOLYSIS, v.29, n.1, p.32-40, 2010

0929-5305

http://producao.usp.br/handle/BDPI/24167

10.1007/s11239-009-0321-7

http://dx.doi.org/10.1007/s11239-009-0321-7

Idioma(s)

eng

Publicador

SPRINGER

Relação

Journal of Thrombosis and Thrombolysis

Direitos

restrictedAccess

Copyright SPRINGER

Palavras-Chave #Coronary artery disease #Homocysteine #Genetic polymorphisms #Methylmalonic acid #METHYLENETETRAHYDROFOLATE REDUCTASE GENE #INTRODUCTION MASS-SPECTROMETRY #METHIONINE SYNTHASE #MYOCARDIAL-INFARCTION #SERUM HOMOCYSTEINE #C677T MUTATION #HEART-DISEASE #FOLIC-ACID #RAT-LIVER #MTHFR #Hematology #Peripheral Vascular Disease
Tipo

article

original article

publishedVersion