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

Beskrivning

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 ≤ 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.
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Publiceringsår

2024

Typ av data

Upphovspersoner

Kati Heinonen - Upphovsperson

Taylor & Francis - Utgivare

Unknown organization

Alexander Neumann - Upphovsperson

Christian M. Page - Upphovsperson

Christine Louise Parr - Upphovsperson

Edwina H. Yeung - Upphovsperson

Elizabeth W. Diemer - Upphovsperson

Emily Oken - Upphovsperson

Henning M. Tiemeier - Upphovsperson

Janine Frédérique Felix - Upphovsperson

Jari Lahti - Upphovsperson

Jianping Jin - Upphovsperson

Johanna Tuhkanen - Upphovsperson

L. Bouchard - Upphovsperson

Maria Christine Magnus - Upphovsperson

Marie France Hivert - Upphovsperson

Matthew J. Suderman - Upphovsperson

Patrice Perron - Upphovsperson

Ruby Fore - Upphovsperson

Sara Sammallahti - Upphovsperson

Sheryl L. Rifas-Shiman - Upphovsperson

Siri E. Håberg - Upphovsperson

Sonia L. Robinson - Upphovsperson

Stephanie J. London - Upphovsperson

Sunni L. Mumford - Upphovsperson

Weihua Guan - Upphovsperson

Wenche Nystad - Upphovsperson

Projekt

Övriga uppgifter

Vetenskapsområden

Biomedicinska vetenskaper

Språk

engelska

Öppen tillgång

Öppet

Licens

Creative Commons Attribution 4.0 International (CC BY 4.0)

Nyckelord

genetics, Science Policy, Biotechnology, Medicine, FOS: Biological sciences, Developmental Biology, Hematology

Ämnesord

cell biology

Temporal täckning

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