Maternal-Infant Factors in Relation to Extracellular Vesicle and Particle miRNA in Prenatal Plasma and in Postpartum Human Milk

• Published in: International journal of molecular sciences Vol. 25; no. 3; p. 1538
• Main Authors: Muse, Meghan E, Armstrong, David A, Hoen, Anne G, Gilbert-Diamond, Diane, Gui, Jiang, Palys, Thomas J, Kolling, Frederick W, Christensen, Brock C, Karagas, Margaret R, Howe, Caitlin G
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.02.2024
• Subjects: Analysis; Babies; Cesarean Section; Cohort Studies; Communication; Epigenesis, Genetic; Epigenetics; Extracellular Vesicles - genetics; Extracellular Vesicles - metabolism; extracellular vesicles and particles; Female; Gene expression; Gestational age; Gestational diabetes; human milk; Humans; Infant; Infants; Influence; MicroRNA; MicroRNAs; MicroRNAs - metabolism; Milk, Human - metabolism; miRNA; Parity; Pilot Projects; Plasma; Postpartum Period; Preeclampsia; Pregnancy; Pregnant women; Lebanon; New Hampshire; miRNA; extracellular vesicles and particles; human milk; plasma; pregnancy
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25031538

MicroRNAs (miRNA) in extracellular vesicles and particles (EVPs) in maternal circulation during pregnancy and in human milk postpartum are hypothesized to facilitate maternal-offspring communication via epigenetic regulation. However, factors influencing maternal EVP miRNA profiles during these two critical developmental windows remain largely unknown. In a pilot study of 54 mother-child dyads in the New Hampshire Birth Cohort Study, we profiled 798 EVP miRNAs, using the NanoString nCounter platform, in paired maternal second-trimester plasma and mature (6-week) milk samples. In adjusted models, total EVP miRNA counts were lower for plasma samples collected in the afternoon compared with the morning ( = 0.024). Infant age at sample collection was inversely associated with total miRNA counts in human milk EVPs ( = 0.040). Milk EVP miRNA counts were also lower among participants who were multiparous after delivery ( = 0.047), had a pre-pregnancy BMI > 25 kg/m ( = 0.037), or delivered their baby via cesarean section ( = 0.021). In post hoc analyses, we also identified 22 specific EVP miRNA that were lower among participants who delivered their baby via cesarean section ( < 0.05). Target genes of delivery mode-associated miRNAs were over-represented in pathways related to satiety signaling in infants (e.g., CCKR signaling) and mammary gland development and lactation (e.g., FGF signaling, EGF receptor signaling). In conclusion, we identified several key factors that may influence maternal EVP miRNA composition during two critical developmental windows, which should be considered in future studies investigating EVP miRNA roles in maternal and child health.