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Maternal iron status in early pregnancy and DNA methylation in offspring: an epigenome-wide meta-analysis.
Taeubert, M J; de Prado-Bert, P; Geurtsen, M L; Mancano, G; Vermeulen, M J; Reiss, I K M; Caramaschi, D; Sunyer, J; Sharp, G C; Julvez, J; Muckenthaler, M U; Felix, J F.
Afiliación
  • Taeubert MJ; The Generation R Study Group, Erasmus University Medical Center, PO Box 2040, 3000 CA, Rotterdam, The Netherlands.
  • de Prado-Bert P; Department of Pediatric Oncology, Hematology and Immunology, University Medical Center Heidelberg, Heidelberg, Germany.
  • Geurtsen ML; ISGlobal, Barcelona, Spain.
  • Mancano G; Universitat Pompeu Fabra (UPF), Barcelona, Spain.
  • Vermeulen MJ; CIBER Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.
  • Reiss IKM; The Generation R Study Group, Erasmus University Medical Center, PO Box 2040, 3000 CA, Rotterdam, The Netherlands.
  • Caramaschi D; Department of Pediatrics, Sophia's Children's Hospital, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
  • Sunyer J; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
  • Sharp GC; Bristol Medical School Population Health Sciences, University of Bristol, Bristol, UK.
  • Julvez J; Department of Pediatrics, Sophia's Children's Hospital, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
  • Muckenthaler MU; Department of Pediatrics, Sophia's Children's Hospital, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
  • Felix JF; College of Life and Environmental Sciences, Psychology, University of Exeter, Exeter, UK.
Clin Epigenetics ; 14(1): 59, 2022 05 03.
Article en En | MEDLINE | ID: mdl-35505416
BACKGROUND: Unbalanced iron homeostasis in pregnancy is associated with an increased risk of adverse birth and childhood health outcomes. DNA methylation has been suggested as a potential underlying mechanism linking environmental exposures such as micronutrient status during pregnancy with offspring health. We performed a meta-analysis on the association of maternal early-pregnancy serum ferritin concentrations, as a marker of body iron stores, and cord blood DNA methylation. We included 1286 mother-newborn pairs from two population-based prospective cohorts. Serum ferritin concentrations were measured in early pregnancy. DNA methylation was measured with the Infinium HumanMethylation450 BeadChip (Illumina). We examined epigenome-wide associations of maternal early-pregnancy serum ferritin and cord blood DNA methylation using robust linear regression analyses, with adjustment for confounders and performed fixed-effects meta-analyses. We additionally examined whether associations of any CpGs identified in cord blood persisted in the peripheral blood of older children and explored associations with other markers of maternal iron status. We also examined whether similar findings were present in the association of cord blood serum ferritin concentrations with cord blood DNA methylation. RESULTS: Maternal early-pregnancy serum ferritin concentrations were inversely associated with DNA methylation at two CpGs (cg02806645 and cg06322988) in PRR23A and one CpG (cg04468817) in PRSS22. Associations at two of these CpG sites persisted at each of the follow-up time points in childhood. Cord blood serum ferritin concentrations were not associated with cord blood DNA methylation levels at the three identified CpGs. CONCLUSION: Maternal early-pregnancy serum ferritin concentrations were associated with lower cord blood DNA methylation levels at three CpGs and these associations partly persisted in older children. Further studies are needed to uncover the role of these CpGs in the underlying mechanisms of the associations of maternal iron status and offspring health outcomes.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Metilación de ADN / Epigenoma Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Adolescent / Child / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Clin Epigenetics Año: 2022 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Metilación de ADN / Epigenoma Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Adolescent / Child / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Clin Epigenetics Año: 2022 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Alemania