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Maternal smoking during pregnancy is associated with DNA methylation in early adolescence

A sibling comparison design

Bibliographic Data

ID9792129
AuthorsNikolina Nonkovic (corresponding author), Kristine Marceau (0000-0002-8924-6597), John E McGeary (0000-0003-4025-9511, John Brown University), Amanda M Ramos (0000-0001-7391-1428, University of North Carolina at Chapel Hill), Rohan H Palmer (0000-0002-6809-9962), Rohan H C Palmer, Andrew C Heath (0000-0002-9414-6857, Washington University in St. Louis), Valerie S Knopik (0000-0002-5727-0576)
Year2024
Volume60
Issue9
Pages1639-1654
Publication date2024-09-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueDevelopmental Psychology (JOURNAL)
Journal identifiersISSN: 0012-1649 • E-ISSN: 1939-0599
PublisherAmerican Psychological Association (APA) (PUBLISHER)
DOI10.1037/dev0001747
PMID38661663
OpenAlexW4395465025
LanguageEN

Maternal smoking during pregnancy (MSDP) may impact offspring biological (e.g., deoxyribonucleic acid methylation [DNAm]) and behavioral (e.g., attention-deficit/hyperactivity disorder hyperactive/impulsive [ADHD-HI] symptoms) development. There has been consistency in findings of differential methylation in global DNAm, and the specific genes AHRR, CYP1A1, CNTNAP2, MYO1G, and GFI1 in relation to MSDP. The current study aims to (a) replicate the associations of MSDP and DNAm in prior literature in middle childhood-adolescence (cross-sectionally) using a sibling-comparison design where siblings were discordant for MSDP ( n = 328 families; M age Sibling 1 = 13.02; Sibling 2 = 10.20), adjusting for prenatal and postnatal covariates in order to isolate the MSDP exposure on DNAm. We also (b) cross-sectionally explored the role of DNAm in the most robust MSDP-ADHD associations (i.e., with ADHD-HI) previously found in this sample. We quantified smoking exposure severity for each sibling reflecting time and quantity of MSDP, centered relative to the sibling pair's average (i.e., within-family centered, indicating child-specific effects attributable MSDP exposure) and controlling for the sibling average MSDP (i.e., between-family component, indicating familial confounding related to MSDP). We found that child-specific MSDP was associated with global DNAm, and CNTNAP2, CYP1A1, and MYO1G methylation after covariate adjustment, corroborating emerging evidence for a potentially causal pathway between MSDP and DNAm. There was some evidence that child-specific CNTNAP2 and MYO1G methylation partially explained associations between MSDP and ADHD-HI symptoms, though only on one measure (of two). Future studies focused on replication of these findings in a longitudinal genetic design could further solidify the associations found in the current study. (PsycInfo Database Record (c) 2024 APA, all rights reserved)

Biology · Cognition · Developmental psychology · DNA methylation · dNaM · Gene · Methylation · Offspring · Pregnancy · Psychiatry · Sibling · Attention Deficit Hyperactivity Disorder · Breastfeeding Practices and Influences · Clinical Psychology · Epigenetics and DNA Methylation · Genetics · Pediatric health and respiratory diseases · Psychology

Citation velocityhistorical
Highly citedNo

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