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Differential effects of the methylenetetrahydrofolate reductase polymorphisms (C677T and A1298C) on hematological malignancies among Latinos: a meta-analysis.
Garcia-Hernandez, Samanta Celeste; Meneses-Sanchez, Perla; Porchia, Leonardo Martin; Torres-Rasgado, Enrique; Pérez-Fuentes, Ricardo; Gonzalez-Mejia, Martha Elba.
Afiliação
  • Garcia-Hernandez SC; Departamento de Genética, Facultad de Medicina, Benémerita Universidad Autónoma de Puebla. Puebla, Mexico.
  • Meneses-Sanchez P; Departamento de Genética, Facultad de Medicina, Benémerita Universidad Autónoma de Puebla. Puebla, Mexico.
  • Porchia LM; Laboratorio de Investigación en Fisiopatología de Enfermedades Crónicas, Centro de Investigación Biomédica de Oriente, IMSS, Delegación Puebla. Atlixco, Puebla, Mexico.
  • Torres-Rasgado E; Facultad de Medicina, Benemérita Universidad Autónoma de Puebla. Puebla, Mexico.
  • Pérez-Fuentes R; Laboratorio de Investigación en Fisiopatología de Enfermedades Crónicas, Centro de Investigación Biomédica de Oriente, IMSS, Delegación Puebla. Atlixco, Puebla, Mexico.
  • Gonzalez-Mejia ME; Facultad de Medicina, Benemérita Universidad Autónoma de Puebla. Puebla, Mexico.
Genet Mol Biol ; 42(3): 549-559, 2019.
Article em En | MEDLINE | ID: mdl-31188929
Our objective was to determine the association between the methylenetetrahydrofolate reductase polymorphisms (C677T and A1298C) and the risk of developing acute lymphoblastic leukemia (ALL), chronic myeloid leukemia (CML), acute myeloid leukemia (AML), and multiple myelomas (MM) in Latinos. PubMed, SCOPUS, EBSCO, LILACS, and other Latin-specific databases were searched for case-control studies that investigated the association between these polymorphisms and hematologic malignancies until November 2017. Genotype distributions were extracted and either fixed-effects or random-effects models were used to calculate the pooled crude odds ratios (ORs) for the heterozygous, homozygous, dominant, recessive, and allelic genetic models. No publication bias was detected by the Begg-Mazumdar's test and Egger's test. From 290 publications, we identified 15 studies on the C677T polymorphism and 13 studies on the A1298C polymorphism. We observed a significant decrease in risk for the C677T polymorphism (OR range=0.54-0.75, p<0.01) and a significant increase in risk for the A1298C polymorphism (OR range=1.28-2.52, p<0.05) in developing ALL for all genetic models. No associations were determined for CML, AML, or MM for either polymorphism. This meta-analysis demonstrated that the A1298C polymorphism was associated with an increased risk of developing ALL, whereas the C677T polymorphism was associated with a decreased risk (protective factor) in the Latino population.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Idioma: En Revista: Genet Mol Biol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: México País de publicação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Idioma: En Revista: Genet Mol Biol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: México País de publicação: Brasil