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Maternal asthma and newborn DNA methylation
Copenhagen Prospective Studies On Asthma in Childhood, Herlev and Gentofte Hospital, COPSAC, University of Copenhagen, Ledreborg Alle 34 Gentofte, Copenhagen, Denmark.
Division of Intramural Research, National Institute of Environmental Health Sciences (NIEHS), National Institutes of Health (NIH), PO 12233, MD A3-05, NC, Research Triangle Park, United States; Department of Pediatrics, Division of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, TX, Houston, United States; Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, TX, Houston, United States; Cancer and Hematology Center, Texas Children’s Hospital, TX, Houston, United States.
Division of Intramural Research, National Institute of Environmental Health Sciences (NIEHS), National Institutes of Health (NIH), PO 12233, MD A3-05, NC, Research Triangle Park, United States.
Department of Biomedicine, Aarhus University, Aarhus, Denmark; Center for Genomics and Personalized Medicine, CGPM, and Center for Integrative Sequencing, iSEQ, Aarhus University, Aarhus, Denmark; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, Denmark.
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2025 (English)In: Clinical Epigenetics, E-ISSN 1868-7083, Vol. 17, no 1, article id 79Article in journal (Refereed) Published
Abstract [en]

Background: Prenatal exposure to maternal asthma may influence DNA methylation patterns in offspring, potentially affecting their susceptibility to later diseases including asthma.

Objective: To investigate the relationship between parental asthma and newborn blood DNA methylation.

Methods: Epigenome-wide association analyses were conducted in 13 cohorts on 7433 newborns with blood methylation data from the Illumina450K or EPIC array. We used fixed effects meta-analyses to identify differentially methylated CpGs (DMCs) and comb-p to identify differentially methylated regions (DMRs) associated with maternal asthma during pregnancy and maternal asthma ever. Paternal asthma was analyzed for comparison. Models were adjusted for covariates and cell-type composition. We examined whether implicated sites related to gene expression analyses in publicly available data for childhood blood and adult lung.

Results: We identified 27 CpGs associated with maternal asthma during pregnancy at False Discovery Rate < 0.05 but none for maternal asthma ever. Two distinct CpGs were associated with paternal asthma. We observed 5 DMRs associated with maternal asthma during pregnancy 3 associated with maternal asthma ever and 13 DMRs associated with paternal asthma. Gene expression analysis using data in blood from 832 children and lung from 424 adults showed associations between identified DMCs using maternal asthma and expression of several genes, including HLA genes and HOXA5, previously implicated in asthma or lung function.

Conclusion: Parental asthma, especially maternal asthma during pregnancy, may be associated with alterations in newborn DNA methylation. These findings might shed light on underlying mechanisms for asthma susceptibility.

Place, publisher, year, edition, pages
BioMed Central (BMC), 2025. Vol. 17, no 1, article id 79
National Category
Respiratory Medicine and Allergy
Identifiers
URN: urn:nbn:se:umu:diva-239103DOI: 10.1186/s13148-025-01858-4ISI: 001485659400001PubMedID: 40349045Scopus ID: 2-s2.0-105004887387OAI: oai:DiVA.org:umu-239103DiVA, id: diva2:1961854
Available from: 2025-05-28 Created: 2025-05-28 Last updated: 2025-05-28Bibliographically approved

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Harlid, SophiaHarbs, JustinDomellöf, MagnusWest, Christina E.

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