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1.
Clin Epigenetics ; 14(1): 59, 2022 05 03.
Artículo en Inglés | MEDLINE | ID: mdl-35505416

RESUMEN

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.


Asunto(s)
Metilación de ADN , Epigenoma , Adolescente , Niño , Epigénesis Genética , Femenino , Ferritinas/genética , Estudio de Asociación del Genoma Completo , Humanos , Recién Nacido , Hierro , Embarazo , Estudios Prospectivos
2.
Ned Tijdschr Geneeskd ; 160: D130, 2016.
Artículo en Holandés | MEDLINE | ID: mdl-27229695

RESUMEN

At the outpatient clinic, an 8-month-old girl presented with a black hairy tongue. Since 2,5 weeks she used antibiotics because of osteomyelitis in her right humerus. There was no proper oral hygiene. She had no other complaints or abnormalities. The diagnosis 'lingua villosa nigra' was made. This is a benign, self-limiting disorder.


Asunto(s)
Lengua Vellosa/patología , Antibacterianos/uso terapéutico , Femenino , Humanos , Lactante , Higiene Bucal , Osteomielitis/tratamiento farmacológico
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