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DNA Methylation in Newborns and Maternal Smoking in Pregnancy
- Source :
- American Journal of Human Genetics, 98(4), 680-696. Cell Press, American Journal of Human Genetics, 98(4), 680. Cell Press, American Journal of Human Genetics, 98(4), 680-696. CELL PRESS, The American Journal of Human Genetics, Recercat. Dipósit de la Recerca de Catalunya, instname
- Publication Year :
- 2016
- Publisher :
- CELL PRESS, 2016.
-
Abstract
- Epigenetic modifications, including DNA methylation, represent a potential mechanism for environmental impacts on human disease. Maternal smoking in pregnancy remains an important public health problem that impacts child health in a myriad of ways and has potential lifelong consequences. The mechanisms are largely unknown, but epigenetics most likely plays a role. We formed the Pregnancy And Childhood Epigenetics (PACE) consortium and meta-analyzed, across 13 cohorts (n = 6,685), the association between maternal smoking in pregnancy and newborn blood DNA methylation at over 450,000 CpG sites (CpGs) by using the Illumina 450K BeadChip. Over 6,000 CpGs were differentially methylated in relation to maternal smoking at genome-wide statistical significance (false discovery rate, 5%), including 2,965 CpGs corresponding to 2,017 genes not previously related to smoking and methylation in either newborns or adults. Several genes are relevant to diseases that can be caused by maternal smoking (e.g., orofacial clefts and asthma) or adult smoking (e.g., certain cancers). A number of differentially methylated CpGs were associated with gene expression. We observed enrichment in pathways and processes critical to development. In older children (5 cohorts, n = 3,187), 100% of CpGs gave at least nominal levels of significance, far more than expected by chance (p value < 2.2 × 10−16). Results were robust to different normalization methods used across studies and cell type adjustment. In this large scale meta-analysis of methylation data, we identified numerous loci involved in response to maternal smoking in pregnancy with persistence into later childhood and provide insights into mechanisms underlying effects of this important exposure. The BAMSE cohort was supported by The Swedish Research Council, The Swedish Heart-Lung Foundation, Freemason Child House Foundation in Stockholm, MeDALL (Mechanisms of the Development of ALLergy), a collaborative project conducted within the European Union (grant agreement No. 261357), Centre for Allergy Research, Stockholm County Council (ALF), Swedish foundation for strategic research (SSF, RBc08-0027, EpiGene project), the Strategic Research Programme (SFO) in Epidemiology at Karolinska Institutet, The Swedish Research Council Formas and the Swedish Environment Protection Agency.
- Subjects :
- 0301 basic medicine
AUTISM SPECTRUM DISORDERS
Bioinformatics
Epigenesis, Genetic
Pregnancy
HYDROCARBON RECEPTOR REPRESSOR
POSTSYNAPTIC DENSITY
Genetics(clinical)
Child
NEUROPILIN-2 EXPRESSION
Genetics (clinical)
Genetics
Smoking
Chromosome Mapping
Methylation
3. Good health
Cleft Palate
CpG site
Meta-analysis
Child, Preschool
DNA methylation
Female
medicine.medical_specialty
Cleft Lip
European Continental Ancestry Group
IN-UTERO
Biology
Article
White People
03 medical and health sciences
Genetic
LUNG-FUNCTION DECLINE
medicine
Journal Article
Humans
BREAST-CANCER
Epigenetics
Preschool
Genetic Association Studies
Asthma
PRENATAL EXPOSURE
Public health
Infant, Newborn
LYMPH-NODE METASTASIS
Infant
DNA Methylation
medicine.disease
Newborn
030104 developmental biology
CIGARETTE-SMOKING
Epigenesis
Meta-Analysis
Subjects
Details
- Language :
- English
- ISSN :
- 00029297
- Volume :
- 98
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- American Journal of Human Genetics
- Accession number :
- edsair.doi.dedup.....a15183f3d57162432590ba820f8ffac6
- Full Text :
- https://doi.org/10.1016/j.ajhg.2016.02.019