Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/195839
Type: Artigo de periódico
Title: Polymorphisms In The Methylenetetrahydrofolate Reductase And Methionine Synthase Reductase Genes And Homocysteine Levels In Brazilian Children.
Author: Aléssio, Ana Claudia M
Annichino-Bizzacchi, Joyce M
Bydlowski, Sergio P
Eberlin, Marcos N
Vellasco, Adriana P
Höehr, Nelci Fenalti
Abstract: Hyperhomocysteinemia is a risk factor for thrombosis, and methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) polymorphisms, folate, and B12 levels could contribute to plasma homocysteine (Hcy) variation. Although well established in adults, few studies have been performed in childhood. In this study, we investigated association of polymorphisms C677T and A1298C in the MTHFR gene and A66G in the MTRR gene with Hcy levels in children. These polymorphisms, as well as Hcy, folate, and vitamin B12 levels were investigated in 220 normal children with ages ranging from 1 to 8 years. Plasma Hcy, folate, and vitamin B12 levels were normal in all children. None of the polymorphisms could be considered an independent risk factor for hyperhomocysteinemia during childhood. The median Hcy levels in 37 children (17%) doubly heterozygous for C677T and A1298C mutations in the MTHFR gene were not different from the other genotypes. However, the association of the different genotypes with Hcy, folate, and vitamin B12 levels demonstrated significant P-values. The folate levels demonstrated a statistically significant decrease (P = 0.0477) from the C677T mutation in the MTHFR gene (TT genotype) when compared to the other groups. Folate was the only independent risk factor for hyperhomocysteinemia. Thus, monitoring the concentrations of folate would be more helpful for evaluating hyperhomocysteinemia and for preventing cardiovascular disease.
Subject: Brazil
Child
Child, Preschool
Ferredoxin-nadp Reductase
Folic Acid
Homocysteine
Humans
Hyperhomocysteinemia
Infant
Methylenetetrahydrofolate Reductase (nadph2)
Polymorphism, Genetic
Risk Factors
Vitamin B 12
Rights: fechado
Identifier DOI: 10.1002/ajmg.a.30108
Address: http://www.ncbi.nlm.nih.gov/pubmed/15216546
Date Issue: 2004
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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