Journal Article

Folic acid supplementation, MTHFR and MTRR polymorphisms, and the risk of childhood leukemia: the ESCALE study (SFCE)

Nelken, Brigitte, Leverger, Guy, Plat, Geneviève, Amigou, Alicia, Rudant, Jérémie, Michel, Gérard, Clavel, Jacqueline, Haouy, Stéphanie, Ducassou, Stéphane, Baruchel, André, Hémon, Denis, Goujon-Bellec, Stéphanie, Rialland, Xavier, Orsi, Laurent, Bertrand, Yves, Chastagner, Pascal

2012

Overview

Purpose: Fetal folate deficiency may increase the risk of subsequent childhood acute leukemia (AL), since folates are required for DNA methylation, synthesis, and repair, but the literature remains scarce. This study tested the hypothesis that maternal folic acid supplementation before or during pregnancy reduces AL risk, accounting for the SNPs rs1801133 (C677T) and rs1801131 (A1298C) in MTHFR and rs1801394 (A66G) and rs1532268 (C524T) in MTRR, assumed to modify folate metabolism. Methods: The nationwide registry-based case-control study, ESCALE, carried out in 2003-2004, included 764 AL cases and 1,681 controls frequency matched with the cases on age and gender. Information on folic acid supplementation was obtained by standardized telephone interview. The genotypes were obtained using high-throughput platforms and imputation for untyped polymorphisms. Odds ratios (OR) were estimated using unconditional regression models adjusted for potential confounders. Results: AL was significantly inversely associated with maternal folic acid supplementation before and during pregnancy (OR = 0.4; 95 % confidence interval: [0.3-0.6]). MTHFR and MTRR genetic polymorphisms were not associated with AL. However, AL was positively associated with homozygosity for any of the MTHFR polymorphisms and carriership of both MTRR variant alleles (OR = 1.6 [0.9-3.1]). No interaction was observed between MTHFR, MTRR, and maternal folate supplementation. Conclusion: The study findings support the hypothesis that maternal folic acid supplementation may reduce the risk of childhood AL. The findings also suggest that the genotype homozygous for any of the MTHFR variants and carrying both MTRR variants could be a risk factor for AL.

• Publisher: Springer,Springer Netherlands,Springer Nature B.V,Springer Verlag
• Subject: Acids / Acute nonlymphocytic leukemia / Alleles / Biomedical and Life Sciences / Biomedicine / Cancer / Cancer Research / Case-Control Studies / Child, Preschool / Childhood / Children / Dietary Supplements / DNA methylation / Epidemiology / Female / Ferredoxin-NADP Reductase - genetics / Folic acid / Folic Acid - administration & dosage / Folic Acid Deficiency - drug therapy / Folic Acid Deficiency - enzymology / Folic Acid Deficiency - genetics / Folic Acid Deficiency - prevention & control / Genetic Predisposition to Disease / Genotypes / Hematology / Humans / Hypotheses / Infant, Newborn / Leukemia / Life Sciences / Lymphocytic leukemia / Male / Metabolism / Methylenetetrahydrofolate Reductase (NADPH2) - genetics / Mothers / Oncology / Original Paper / Polymorphism, Single Nucleotide / Precursor Cell Lymphoblastic Leukemia-Lymphoma - enzymology / Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics / Precursor Cell Lymphoblastic Leukemia-Lymphoma - prevention & control / Pregnancy / Pregnancy Complications - drug therapy / Pregnancy Complications - enzymology / Pregnancy Complications - genetics / Pregnancy Complications - prevention & control / Public Health / Regression analysis / Risk reduction / Socioeconomic status / Vitamin B