Evidence map›Paper›PMID 40667220›Full record

ArticlebioRxiv : the preprint server for biology2025

Immune pathways and perinatal environmental exposures contribute to epigenetic gestational age prediction and acceleration.

Amy A Eapen, Ian M Loveless, Mingming Pan, Xiaoyu Liang, Audrey Urquhart, Jennifer Straughen, Andrea E Cassidy-Bushrow, Alexandra R Sitarik, Neil Simmerman, Emma E Thompson and 5 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

15 authors.

Amy A EapenDivision of Allergy and Clinical Immunology, Department of Internal Medicine, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI.
Ian M LovelessCenter for Bioinformatics, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI.
Mingming PanCenter for Bioinformatics, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI.
Xiaoyu LiangDepartment of Epidemiology and Biostatistics, Michigan State University, Lansing, MI.
Audrey UrquhartDepartment of Public Health Sciences, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI.
Jennifer StraughenDepartment of Public Health Sciences, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI.
Andrea E Cassidy-BushrowDepartment of Public Health Sciences, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI.
Alexandra R SitarikCenter for Bioinformatics, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI.
Neil SimmermanDepartment of Women's Health Services, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI.
Emma E ThompsonDepartment of Human Genetics, University of Chicago, Chicago, IL.
Leah KottyanCenter of Autoimmune Genomics and Etiology, Division of Eosinophilic Disorders, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Carole OberDepartment of Human Genetics, University of Chicago, Chicago, IL.
Christine C JohnsonCenter for Bioinformatics, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI.
Edward ZorattiDivision of Allergy and Clinical Immunology, Department of Internal Medicine, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI.
Albert M LevinCenter for Bioinformatics, Henry Ford Health + Michigan State University Health Sciences, Detroit, MI.

Funding

The Effect of Dog-Keeping and the Intestinal Microbiota on Immune DevelopmentP01AI089473 · NIAID · HENRY FORD HEALTH SYSTEM · PI LUKACS, NICHOLAS W · 2012 to 2024
$25.7M
Delivery mode, environment and the gut microbiome: influence on childhood body sizeR01HD082147 · NICHD · HENRY FORD HEALTH SYSTEM · PI CASSIDY-BUSHROW, ANDREA E · 2016 to 2020
$3.0M
Early Environmental Hygiene and Pediatric AtopyR01AI050681 · NIAID · HENRY FORD HEALTH SYSTEM · PI JOHNSON, CHRISTINE C · 2002 to 2006
$2.9M
NIAID NIH HHS P01 AI089473NIAID NIH HHS R01 AI050681NICHD NIH HHS R01 HD082147
6 · The paper itself

Abstract

DNA methylation (DNAm), capturing biological gestational age (GA) and epigenetic gestational age acceleration (EGAA), can be modified by environmental exposures. The Asthma&Allergy array is a new DNAm array developed with content focused on asthma and allergy loci. The association between content on the Asthma&Allergy array and chronological GA and EGAA has not been evaluated alone or in the context of perinatal exposures. We performed an epigenome wide association study(EWAS) based on chronological GA at single CpG sites and regions. We further constructed a multi-CpG site methylation model to predict chronological GA in cord blood from 391 newborn children from a Detroit-based birth cohort. Associations between perinatal environmental factors with GA, epigenetic gestational age (EGA), and EGAA were assessed. We identified 2,435 CpG sites associated with chronological GA. HLA class II (

Indexed as

Epigenetic gestational age clockGestational agePrenatal environment

Identifiers

PMID40667220
PMCPMC12262535

What OpenQuestion holds

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LicenceCC BY-ND
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Registered trials

None linked

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.