Differential effects of the methylenetetrahydrofolate reductase polymorphisms (C677T and A1298C) on hematological malignancies among Latinos: a meta-analysis.


Journal

Genetics and molecular biology
ISSN: 1415-4757
Titre abrégé: Genet Mol Biol
Pays: Brazil
ID NLM: 100883590

Informations de publication

Date de publication:
Historique:
received: 30 05 2018
accepted: 10 12 2018
pubmed: 13 6 2019
medline: 13 6 2019
entrez: 13 6 2019
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 31188929
pii: S1415-47572019005022102
doi: 10.1590/1678-4685-GMB-2018-0161
pmc: PMC6905449
pii:
doi:

Types de publication

Journal Article

Langues

eng

Pagination

549-559

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Auteurs

Samanta Celeste Garcia-Hernandez (SC)

Departamento de Genética, Facultad de Medicina, Benémerita Universidad Autónoma de Puebla. Puebla, Mexico.

Perla Meneses-Sanchez (P)

Departamento de Genética, Facultad de Medicina, Benémerita Universidad Autónoma de Puebla. Puebla, Mexico.

Leonardo Martin Porchia (LM)

Laboratorio de Investigación en Fisiopatología de Enfermedades Crónicas, Centro de Investigación Biomédica de Oriente, IMSS, Delegación Puebla. Atlixco, Puebla, Mexico.

Enrique Torres-Rasgado (E)

Facultad de Medicina, Benemérita Universidad Autónoma de Puebla. Puebla, Mexico.

Ricardo Pérez-Fuentes (R)

Laboratorio de Investigación en Fisiopatología de Enfermedades Crónicas, Centro de Investigación Biomédica de Oriente, IMSS, Delegación Puebla. Atlixco, Puebla, Mexico.
Facultad de Medicina, Benemérita Universidad Autónoma de Puebla. Puebla, Mexico.

Martha Elba Gonzalez-Mejia (ME)

Departamento de Genética, Facultad de Medicina, Benémerita Universidad Autónoma de Puebla. Puebla, Mexico.

Classifications MeSH