Effect of Prenatal Opioid Exposure on the Human Placental Methylome

• Published in: Biomedicines Vol. 10; no. 5; p. 1150
• Main Authors: Borrelli, Kristyn N, Wachman, Elisha M, Beierle, Jacob A, Taglauer, Elizabeth S, Jain, Mayuri, Bryant, Camron D, Zhang, Huiping
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 17.05.2022; MDPI
• Subjects: Babies; Childbirth & labor; CpG islands; differential methylation; DNA methylation; DNA methylome; Drug addiction; Drug withdrawal; Epigenetics; Fetuses; functional annotation; Gene expression; Gene regulation; Genetic testing; Genomes; Genomics; Gestational age; Narcotics; Neonatal abstinence syndrome; neonatal opioid withdrawal syndrome; Neonates; Nervous system; Opioids; Placenta; Pregnancy; Prenatal experience; prenatal opioid exposure; Research methodology; Substance abuse treatment; Synaptic transmission; Toxicology; Withdrawal; United States > US; DNA methylome; neonatal opioid withdrawal syndrome; placenta; differential methylation; functional annotation; prenatal opioid exposure
• ISSN: 2227-9059; 2227-9059
• DOI: 10.3390/biomedicines10051150

Prenatal exposure to addictive drugs can lead to placental epigenetic modifications, but a methylome-wide evaluation of placental DNA methylation changes after prenatal opioid exposure has not yet been performed. Placental tissue samples were collected at delivery from 19 opioid-exposed and 20 unexposed control full-term pregnancies. Placental DNA methylomes were profiled using the Illumina Infinium HumanMethylationEPIC BeadChip. Differentially methylated CpG sites associated with opioid exposure were identified with a linear model using the ‘limma’ R package. To identify differentially methylated regions (DMRs) spanning multiple CpG sites, the ‘DMRcate’ R package was used. The functions of genes mapped by differentially methylated CpG sites and DMRs were further annotated using Enrichr. Differentially methylated CpGs (n = 684, unadjusted p < 0.005 and |∆β| ≥ 0.05) were mapped to 258 genes (including PLD1, MGAM, and ALCS2). Differentially methylated regions (n = 199) were located in 174 genes (including KCNMA1). Enrichment analysis of the top differentially methylated CpG sites and regions indicated disrupted epigenetic regulation of genes involved in synaptic structure, chemical synaptic transmission, and nervous system development. Our findings imply that placental epigenetic changes due to prenatal opioid exposure could result in placental dysfunction, leading to abnormal fetal brain development and the symptoms of opioid withdrawal in neonates.