DNA methylation patterns in newborns exposed to tobacco in utero

• Published in: Journal of translational medicine Vol. 13; no. 1; p. 25
• Main Authors: Ivorra, Carmen, Fraga, Mario F, Bayón, Gustavo F, Fernández, Agustín F, Garcia-Vicent, Consuelo, Chaves, F Javier, Redon, Josep, Lurbe, Empar
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 27-01-2015; BioMed Central
• Subjects: Adrenomedullin - chemistry; Adult; Analysis; Cardiovascular diseases; Cluster Analysis; CpG Islands; DNA; DNA Methylation; Epigenesis, Genetic; Epigenetic inheritance; Epigenomics; Female; Fetal Blood; Fetus; Gene Expression Regulation; Genes; Genetic research; Genome-Wide Association Study; Growth; Health aspects; Humans; Immunoassay; Infant, Newborn; Infants (Newborn); Maternal Exposure; Methylation; Mothers; Nicotiana - adverse effects; Pregnancy; Pregnant women; Risk Factors; Tobacco Smoke Pollution; Type 2 diabetes; Young Adult; Spain
• ISSN: 1479-5876; 1479-5876
• DOI: 10.1186/s12967-015-0384-5

Maternal smoking during pregnancy is a major risk factor for adverse health outcomes. The main objective of the study was to assess the impact of in utero tobacco exposure on DNA methylation in children born at term with appropriate weight at birth.
Twenty mother-newborn dyads, after uncomplicated pregnancies, in the absence of perinatal illness were included. All mothers were healthy with no cardiovascular risk factors, except for the associated risks among those mothers who smoked. Umbilical cord blood and maternal peripheral venous blood were collected and an epigenome-wide association study was performed using a 450 K epigenome-wide scan (Illumina Infinium HumanMethylation 450BeadChip) with adjustment to normalize the DNA methylation for data cell variability in whole blood.
The maternal plasmatic cotinine levels ranged from 10.70-115.40 ng/ml in the exposed group to 0-0.59 ng/ml in the non-exposed group. After adjusting for multiple comparisons in 427102 probes, statistically significant differences for 31 CpG sites, associated to 25 genes were observed. There was a greater than expected proportion of statistically-significant loci located in CpG islands (Fisher's exact test, p = 0.029) and of those CpG islands, 90.3% exhibit higher methylation levels in the exposed group. The most striking and significant CpG site, cg05727225, is located in the chromosome 11p15.4, within the adrenomedullin gene.
In utero tobacco exposure, even in the absence of fetal growth restriction, may alter the epigenome, contributing to global DNA hypomethylation. Therefore, DNA status can be used as a biomarker of prenatal insults. Considering the possibility to reverse epigenetic modifications, a window of opportunity exists to change the programmed chronic disease.