Functional enrichment analysis highlighted the pathways involved in early embryonic development and placental function, implicating early-pregnancy maternal epigenetic alterations in SGA delivery among Black women and supporting DNA methylation profiling as a potential SGA biomarker.
Abstract
Approximately 10% US infants are born small for gestational age (SGA), a condition linked to increased morbidity and mortality. Infants born to Black women are twice as likely to be SGA compared with those born to White women. Although maternal factors, including epigenetic modifications, likely contribute to SGA, the underlying biological mechanisms remain poorly understood. We evaluated whether epigenetic modifications in early pregnancy were associated with SGA among pregnant Black women. We analyzed data from 931 pregnant non-Hispanic Black women (6–13 weeks of gestation) enrolled in the Nulliparous Pregnancy Outcomes Study: Monitoring Mothers-to-be (nuMoM2b) cohort across eight academic medical centers. We conducted an epigenome-wide association study using the Infinium MethylationEPIC assay on blood samples from women who delivered SGA infants (n = 133) and appropriate for gestational age infants (n = 798). We adjusted for maternal age, prenatal smoking, education, body mass index, and infant sex, and corrected with multiple testing. We identified 14 differentially methylated 5'-C-phosphate-G-3' (CpG) sites mapping to genes involved in placental development, vascular remodeling, and fetal growth regulation. Functional enrichment analysis highlighted the pathways involved in early embryonic development and placental function, implicating early-pregnancy maternal epigenetic alterations in SGA delivery among Black women and supporting DNA methylation profiling as a potential SGA biomarker.
Prenatal serum PFAS concentrations were associated with alterations in maternal DNA methylation, which in turn were associated with infant birth size, which in turn was associated with infant birth size.
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DNA methylation is associated with individual differences in birthweight in a high-risk clinical population of MC twins, independent of shared genetic, familial, maternal, and obstetric factors.
M. Sulaiman, L. Franken, J. A. Spekman et al.· medRxiv· 0 citations
Background: Both fetal and maternal genomes contribute to birthweight, but the timing and relative magnitude of their effects during gestation remain unclear. Polygenic risk scores (PRSs), constructed from genome-wide association studies (GWAS), capture the cumulative influence of common birthweight-associated variants...
F. Cates, O. Wootton, J. X. Kiley et al.· medRxiv· 0 citations
B Buccal DNA methylation-derived EpiScores capture biological signatures associated with neonatal morbidity burden in very preterm infants, and reflected immune, inflammatory, metabolic, and growth-related pathways.
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Summary Background Pregnancies complicated by fetal growth restriction (FGR) and preeclampsia are associated with increased long-term chronic disease risk. A blood test could possibly identify those at risk, opening the door to early interventions soon after delivery. Prior work in non-pregnant people have identified p...
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Maternal exposure to adverse childhood experiences (ACEs) may influence aging biomarkers in pediatric populations, as estimated using epigenetic clocks or other measures of aging, such as telomere length. This scoping review aimed to identify and map the available evidence on the association between maternal ACEs a...
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