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Epigenome-wide meta-analysis of prenatal vitamin D insufficiency and cord blood DNA methylation

Title: Epigenome-wide meta-analysis of prenatal vitamin D insufficiency and cord blood DNA methylation
Authors: Elizabeth W. Diemer; Johanna Tuhkanen; Sara Sammallahti; Kati Heinonen; Alexander Neumann; Sonia L. Robinson; Matthew Suderman; Jianping Jin; Christian M. Page; Ruby Fore; Sheryl L. Rifas-Shiman; Emily Oken; Patrice Perron; Luigi Bouchard; Marie France Hivert; Katri Räikköne; Jari Lahti; Edwina H. Yeung; Weihua Guan; Sunni L. Mumford; Maria C. Magnus; Siri Håberg; Wenche Nystad; Christine L. Parr; Stephanie J. London; Janine F. Felix; Henning Tiemeier
Source: Epigenetics, Vol 19, Iss 1 (2024)
Publisher Information: Taylor & Francis Group, 2024.
Publication Year: 2024
Collection: LCC:Genetics
Subject Terms: Vitamin D insufficiency; EWAS; PACE; DNA methylation; epigenetics; Vitamin D; Genetics; QH426-470
Description: Low maternal vitamin D concentrations during pregnancy have been associated with a range of offspring health outcomes. DNA methylation is one mechanism by which the maternal vitamin D status during pregnancy could impact offspring’s health in later life. We aimed to evaluate whether maternal vitamin D insufficiency during pregnancy was conditionally associated with DNA methylation in the offspring cord blood. Maternal vitamin D insufficiency (plasma 25-hydroxy vitamin D [Formula: see text] 75 nmol/L) during pregnancy and offspring cord blood DNA methylation, assessed using Illumina Infinium 450k or Illumina EPIC Beadchip, was collected for 3738 mother–child pairs in 7 cohorts as part of the Pregnancy and Childhood Epigenetics (PACE) consortium. Associations between maternal vitamin D and offspring DNA methylation, adjusted for fetal sex, maternal smoking, maternal age, maternal pre-pregnancy or early pregnancy BMI, maternal education, gestational age at measurement of 25(OH)D, parity, and cell type composition, were estimated using robust linear regression in each cohort, and a fixed-effects meta-analysis was conducted. The prevalence of vitamin D insufficiency ranged from 44.3% to 78.5% across cohorts. Across 364,678 CpG sites, none were associated with maternal vitamin D insufficiency at an epigenome-wide significant level after correcting for multiple testing using Bonferroni correction or a less conservative Benjamini–Hochberg False Discovery Rate approach (FDR, p > 0.05). In this epigenome-wide association study, we did not find convincing evidence of a conditional association of vitamin D insufficiency with offspring DNA methylation at any measured CpG site.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1559-2308; 1559-2294
Relation: https://doaj.org/toc/1559-2294; https://doaj.org/toc/1559-2308
DOI: 10.1080/15592294.2024.2413815
Access URL: https://doaj.org/article/5e8e802a77ca43568fa7aaec9fcc5eb2
Accession Number: edsdoj.5e8e802a77ca43568fa7aaec9fcc5eb2
Database: Directory of Open Access Journals