An epigenome-wide association study of child appetitive traits and DNA methylation.

dc.contributor.author

Harris, Holly A

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Friedman, Chloe

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Starling, Anne P

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Dabelea, Dana

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Johnson, Susan L

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Fuemmeler, Bernard F

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Jima, Dereje

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Murphy, Susan K

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Hoyo, Cathrine

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Jansen, Pauline W

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Felix, Janine F

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Mulder, Rosa H

dc.date.accessioned

2024-03-27T16:32:08Z

dc.date.available

2024-03-27T16:32:08Z

dc.date.issued

2023-10

dc.description.abstract

The etiology of childhood appetitive traits is poorly understood. Early-life epigenetic processes may be involved in the developmental programming of appetite regulation in childhood. One such process is DNA methylation (DNAm), whereby a methyl group is added to a specific part of DNA, where a cytosine base is next to a guanine base, a CpG site. We meta-analyzed epigenome-wide association studies (EWASs) of cord blood DNAm and early-childhood appetitive traits. Data were from two independent cohorts: the Generation R Study (n = 1,086, Rotterdam, the Netherlands) and the Healthy Start study (n = 236, Colorado, USA). DNAm at autosomal methylation sites in cord blood was measured using the Illumina Infinium HumanMethylation450 BeadChip. Parents reported on their child's food responsiveness, emotional undereating, satiety responsiveness and food fussiness using the Children's Eating Behaviour Questionnaire at age 4-5 years. Multiple regression models were used to examine the association of DNAm (predictor) at the individual site- and regional-level (using DMRff) with each appetitive trait (outcome), adjusting for covariates. Bonferroni-correction was applied to adjust for multiple testing. There were no associations of DNAm and any appetitive trait when examining individual CpG-sites. However, when examining multiple CpGs jointly in so-called differentially methylated regions, we identified 45 associations of DNAm with food responsiveness, 7 associations of DNAm with emotional undereating, 13 associations of DNAm with satiety responsiveness, and 9 associations of DNAm with food fussiness. This study shows that DNAm in the newborn may partially explain variation in appetitive traits expressed in early childhood and provides preliminary support for early programming of child appetitive traits through DNAm. Investigating differential DNAm associated with appetitive traits could be an important first step in identifying biological pathways underlying the development of these behaviors.

dc.identifier

S0195-6663(23)02548-5

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0195-6663

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1095-8304

dc.identifier.uri

https://hdl.handle.net/10161/30398

dc.language

eng

dc.publisher

Elsevier BV

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Appetite

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10.1016/j.appet.2023.107086

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https://creativecommons.org/licenses/by-nc/4.0

dc.subject

Appetitive traits

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Childhood

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DNA methylation

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Eating behaviors

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Epigenetics

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Epigenome-wide association study

dc.title

An epigenome-wide association study of child appetitive traits and DNA methylation.

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Journal article

duke.contributor.orcid

Murphy, Susan K|0000-0001-8298-7272

pubs.begin-page

107086

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Duke

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Nicholas School of the Environment

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School of Medicine

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Clinical Science Departments

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Institutes and Centers

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Obstetrics and Gynecology

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Pathology

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Duke Cancer Institute

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Environmental Sciences and Policy

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Obstetrics and Gynecology, Reproductive Sciences

pubs.publication-status

Published

pubs.volume

191

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