Evidence map›Paper›PMID 42789309›Full record

ArticleEpigenetics2026

Differential methylation at novel putative imprinting control regions on chromosome 20 associated with childhood obesity.

Catherine F Everly, Terrence K Allen, David A Skaar, Bruce A Corliss, Dereje D Jima, Rachel L Maguire, Halah Jadallah, Randy L Jirtle, Susan K Murphy, Jung-Ying Tzeng and 1 more

Abstract read
In one paragraph

Article in Epigenetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Catherine F EverlyBioinformatics Research Center, North Carolina State University, Raleigh, NC, USA.ORCID 0009-0005-6918-6936
Terrence K AllenDepartment of Anesthesiology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0003-3904-7618
David A SkaarCenter for Human Health and the Environment, North Carolina State University, Raleigh, NC, USA.ORCID 0000-0003-3530-957X
Bruce A CorlissBioinformatics Research Center, North Carolina State University, Raleigh, NC, USA.ORCID 0000-0003-2962-7344
Dereje D JimaBioinformatics Research Center, North Carolina State University, Raleigh, NC, USA.ORCID 0000-0002-7784-1612
Rachel L MaguireCenter for Human Health and the Environment, North Carolina State University, Raleigh, NC, USA.ORCID 0000-0001-6421-2545
Halah JadallahDepartment of Biological Sciences, North Carolina State University, Raleigh, NC, USA.ORCID 0009-0006-4918-8675
Randy L JirtleCenter for Human Health and the Environment, North Carolina State University, Raleigh, NC, USA.ORCID 0000-0003-1767-045X
Susan K MurphyDepartment of Obstetrics and Gynecology, Division of Reproductive Sciences, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0001-8298-7272
Jung-Ying TzengBioinformatics Research Center, North Carolina State University, Raleigh, NC, USA.ORCID 0000-0002-5505-1775
Cathrine HoyoCenter for Human Health and the Environment, North Carolina State University, Raleigh, NC, USA.ORCID 0000-0002-2466-8617

Funding

Translational Research Support CoreP30ES025128 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Sue Fenton · 2015 to 2026
$18.3M
Prenatal stress and diet, and the fetal epigenomeR01MD017696 · NIMHD · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Cathrine Hoyo · 2022 to 2026
$3.2M
Novel imprint control regions (ICRs) responsive to environmental exposuresR01ES032462 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI HOYO, CATHRINE · 2021 to 2025
$3.0M
NIEHS NIH HHS P30 ES025128NIEHS NIH HHS R01 ES032462NIMHD NIH HHS R01 MD017696
6 · The paper itself

Abstract

DNA methylation may link early-life exposures to later obesity risk; however, most studies examine individual CpG sites using commercial arrays that cover < 5% of the genome and often overlook biologically relevant regulatory regions. Imprinting control regions (ICRs) regulate parent-of-origin gene expression and are enriched for growth and metabolic genes, representing strong candidates for developmental programming of obesity. In 586 participants of the Newborn Epigenetics STudy (NEST), we leveraged the novel Human Imprintome Array to measure methylation at >1,000 characterized and putative ICRs genome-wide in umbilical cord blood. We applied principal component and kernel machine regression to identify ICR methylation at birth associated with sustained childhood obesity, defined as BMI ≥ 95th percentile during most of childhood. Sustained childhood obesity was associated with differential methylation at seven ICRs in cord blood, with 2-10% mean differences between obesity and normal weight groups, including novel regions localized to chromosome 20q11.1-20q11.21 (ICR_1182, ICR_1179, ICR_1181, ICR_1177, ICR_1180, and ICR_1165), mapping to or near

Indexed as

DNA MethylationGenomic ImprintingPediatric ObesityChildCpG IslandsDevelopmental Origins of Health and DiseaseEpigenesis, GeneticFemaleFetal BloodHumansInfant, NewbornMalechildhood obesityDNA methylationImprinting control regions (ICRs)kernel machine (KM) regressionprincipal component (PC) regression

Identifiers

PMID42789309
PMCPMC13618840

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.