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Periconceptional folate intake influences DNA methylation at birth based on dietary source in an analysis of pediatric acute lymphoblastic leukemia cases and controls.
Nickels, Eric M; Li, Shaobo; Morimoto, Libby; Kang, Alice Y; de Smith, Adam J; Metayer, Catherine; Wiemels, Joseph L.
Afiliación
  • Nickels EM; Children's Hospital Los Angeles, Center for Blood Disease Institute, Los Angeles, CA, USA.
  • Li S; University of Southern California Keck School of Medicine, Center for Genetic Epidemiology, Los Angeles, CA, USA.
  • Morimoto L; University of Southern California Keck School of Medicine, Center for Genetic Epidemiology, Los Angeles, CA, USA.
  • Kang AY; School of Public Health, University of California, Berkeley, Berkeley, CA, USA.
  • de Smith AJ; School of Public Health, University of California, Berkeley, Berkeley, CA, USA.
  • Metayer C; University of Southern California Keck School of Medicine, Center for Genetic Epidemiology, Los Angeles, CA, USA.
  • Wiemels JL; School of Public Health, University of California, Berkeley, Berkeley, CA, USA.
Am J Clin Nutr ; 116(6): 1553-1564, 2022 12 19.
Article en En | MEDLINE | ID: mdl-36178055
ABSTRACT

BACKGROUND:

Periconceptional folate intake is associated with the establishment of DNA methylation in offspring; however, variations in this relation by food sources compared with folic acid supplements are not described. Also, maternal folate intake is associated with decreased risk of pediatric acute lymphoblastic leukemia (ALL), but the mechanism is not known.

OBJECTIVES:

We evaluated the relation between periconceptional folate intake by source and DNA methylation at birth in a cohort of pediatric ALL cases and controls in an epigenome-wide association study.

METHODS:

Genome-wide DNA methylation status obtained from archived neonatal blood spots from pediatric ALL cases (n = 189) and controls (n = 205) in the California Childhood Leukemia Study (CCLS) from 1995-2008 was compared with periconceptional folate from total, food, and supplemental sources using multivariable linear regression. Further stratification was performed by income, education, ethnicity, and total folate intake. We evaluated variable DNA methylation response to periconceptional folate by ALL case status through an interaction term.

RESULTS:

Two significant differentially methylated probes (DMPs) were associated with food and supplemental periconceptional folate intake in all subjects (n = 394). The top differentially methylated region at the promoter region of DUSP22(dual specificity phosphatase 22) demonstrated DNA hypermethylation in ALL cases but not in controls in response to total and food folate intake. We further identified 8 interaction term DMPs with variable DNA methylation response to folate intake by ALL case status. Further stratification of the cohort by education and ethnicity revealed a substantially higher number of DMPs associated with supplemental folic acid intake in Hispanic subjects with lower income and educational level.

CONCLUSIONS:

We identified modest associations between periconceptional folate intake and DNA methylation differing by source, including variation by ALL case status. Hispanic subjects of lower income and education appear uniquely responsive to periconceptional folate supplementation.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Leucemia-Linfoma Linfoblástico de Células Precursoras / Ácido Fólico Tipo de estudio: Prognostic_studies Límite: Child / Humans / Newborn Idioma: En Revista: Am J Clin Nutr Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Leucemia-Linfoma Linfoblástico de Células Precursoras / Ácido Fólico Tipo de estudio: Prognostic_studies Límite: Child / Humans / Newborn Idioma: En Revista: Am J Clin Nutr Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos