PLoS ONEGenetic & Genomic MedicinePeer-reviewed journal article
DNA Methylation Differences Stratified by Normalized Fetal/Placental Weight Ratios Suggest Neurodevelopmental Deficits in Neonates with Congenital Heart Disease
Marin JacobwitziD, Hongbo Michael XieiD, Jamie L. CatalanoiD, Ingo HelbigiD, James William GaynoriD, Nancy B. BurnhamiD, Rebecca L. LinniD, Juliana S. GebbiD, Mark W. W. RusselliD, Hakon H. HakonarsoniD, Barbara H. ChaiyachatiiD, Ana G. CristanchoiD
Abstract
BackgroundWe lack early biomarkers for predicting neurodevelopment (ND) outcomes in children with congenital heart disease (CHD). Placentas of fetuses with CHD have abnormalities, including unbalanced fetal/placental weight ratios (F/P). Although DNA methylation profiles have revealed insights into the maternal-fetal environment (MFE), it is unknown if DNA methylation correlates to normalized F/P weight ratio groups and how these differences relate to ND outcomes. MethodsWe prospectively recruited a cohort of pregnant women carrying a fetus with CHD. A subset of the cohort had DNA methylation performed on either umbilical cord blood or postnatal blood (45 full-term neonates). We calculated normalized F/P weight ratios, focusing on three normalized F/P ratio groups for analysis. We calculated differential methylation signals in eight ND disabilities-associated gene sets. Normalized F/P ratios were compared to 18-month Bayley Scales of Infant Development-III scores (BSID-III). ResultsUnbiased gene ontology enrichment analysis of differentially methylated regions revealed enrichment for brain development-related pathways. Although there were no significant differences between normalized F/P weight ratio groups and BSID-III, disease-associated gene set pathway analysis revealed significant methylation differences between the most severely unbalanced F/P weight ratio and normal F/P weight ratio groups. ConclusionGene ontology enrichment analysis of differential methylation regions revealed significant differences between normalized F/P weight ratio groups in neurogenesis genes. Furthermore, our data identified methylation differences between unbalanced and balanced normalized F/P weight ratio groups in gene pathways associated with ND dysfunction common in the aging CHD population suggesting converging pathways for ND disorders that should be investigated further.
- organism: human
- assay: DNA methylation
- research focus: differential expression
- approach: statistical model
- Citations
- 0
- FWCI
- 0.00
- Field percentile
- 22th percentile
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Fetal MRI Reveals Altered Subplate Development in Congenital Heart Disease
Andrea Gondová, Seungyoon Jeong, … Caitlin K. Rollins·bioRxiv·Aug 23, 2026
- Epigenomic signature of major congenital heart defects in newborns with Down syndrome
Julia S. Mouat, Shaobo Li, … Janine M. LaSalle·Human GenomicsPeer-reviewed·Oct 6, 2023
- Delayed maturation of the structural brain connectome in neonates with congenital heart disease
Maria Feldmann, Ting Guo, … Jakab András·Brain CommunicationsPeer-reviewed·Jan 1, 2020
- Placental epigenetics for evaluation of fetal congenital heart defects: Ventricular septal defect (VSD)
Uppala Radhakrishna, Samet Albayrak, … Ray O Bahado-Singh·PLoS ONEPeer-reviewed·Mar 21, 2019
- Multi-omic brain and behavioral correlates of cell-free fetal DNA methylation in macaque maternal obesity models
Benjamin I. Laufer, Yu Hasegawa, … Janine M. LaSalle·Nature CommunicationsPeer-reviewed·Sep 21, 2022
- Unveiling fetal brain changes in congenital diaphragmatic hernia: hypoxic injury with loss of progenitor cells, neurons, and oligodendrocytes
George Biouss, Lina Antounians, … Augusto Zani·bioRxiv·Sep 23, 2023