TY - JOUR
T1 - Associations between maternal lifetime stressors and negative events in pregnancy and breast milk-derived extracellular vesicle microRNAs in the programming of intergenerational stress mechanisms (PRISM) pregnancy cohort
AU - Bozack, Anne K.
AU - Colicino, Elena
AU - Rodosthenous, Rodosthenis
AU - Bloomquist, Tessa R.
AU - Baccarelli, Andrea A.
AU - Wright, Robert O.
AU - Wright, Rosalind J.
AU - Lee, Alison G.
N1 - Funding Information:
The PRogramming of Intergenerational Stress Mechanisms (PRISM) cohort has been supported under US National Institute of Health (NIH) grants R01 HL095606, R01 HL114396, and R01 ES030302 (RJW, Principal Investigator). During the preparation of this manuscript, AGL was supported by US NIH grants R01 MD013310 and K23 HL135349. Analysis of EV-microRNAs was supported in a pilot grant under the US NIH grant P30 ES023515 (AGL, RJW).
Funding Information:
The PRogramming of Intergenerational Stress Mechanisms (PRISM) cohort has been supported under US National Institute of Health (NIH) grants R01 HL095606, R01 HL114396, and R01 ES030302 (RJW, Principal Investigator). During the preparation of this manuscript, AGL was supported by US NIH grants R01 MD013310 and K23 HL135349. Analysis of EV-microRNAs was supported in a pilot grant under the US NIH grant P30 ES023515 (AGL, RJW);National Heart, Lung, and Blood Institute [R01 HL095606];National Heart, Lung, and Blood Institute [K23 HL135349];National Heart, Lung, and Blood Institute [R01 HL114396];National Institute of Environmental Health Sciences [P30 ES023515];National Institute of Environmental Health Sciences [R01 ES030302];National Institute on Minority Health and Health Disparities [R01 MD013310]; The PRogramming of Intergenerational Stress Mechanisms (PRISM) cohort has been supported under US National Institute of Health (NIH) grants R01 HL095606, R01 HL114396, and R01 ES030302 (RJW, Principal Investigator). During the preparation of this manuscript, AGL was supported by US NIH grants R01 MD013310 and K23 HL135349. Analysis of EV-microRNAs was supported in a pilot grant under the US NIH grant P30 ES023515 (AGL, RJW).
Publisher Copyright:
© 2020 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2021
Y1 - 2021
N2 - Maternal stress is associated with adverse child health. Breast milk microRNAs encapsulated in extracellular vesicles (EVs) are involved in mother-infant biochemical communication during early-life programming. We leverage the PRogramming of Intergenerational Stress Mechanisms (PRISM) pregnancy cohort to investigate associations between maternal stress and breast milk EV-microRNAs. Lifetime stress and negative life events (NLEs) during pregnancy were assessed using the Life Stressor Checklist-Revised (LSCR) and the Crisis in Family Systems-Revised surveys, respectively. RNA was extracted from breast milk EVs (N = 80; collected 6.1 ± 5.9 weeks postnatally), and microRNAs were profiled using the TaqMan OpenArray Human miRNA panel. Associations between stress scores and detection (yes/no) of 173 microRNAs identified in 20–80% of samples were assessed using logistic regression; associations with expression levels of 205 EV-microRNAs identified in >50% of samples were assessed using linear regression. In adjusted models, detection of 60 and 44 EV-microRNAs was associated with higher LSCR and NLE scores, respectively (p < 0.05). Expression level of 8 and 17 EV-microRNAs was associated with LSCR and NLE scores, respectively, at our a priori criteria of p < 0.05 and |B regression|>0.2. Enriched KEGG pathways for microRNAs associated with stress scores included fatty acid metabolism and the Hippo signaling pathway. Maternal lifetime stress and NLEs during pregnancy were both associated with detection and expression level of breast milk EV-microRNAs, although associations with microRNA profiles differed between stress measures. Further research is needed to identify biological pathways impacted by associated microRNAs and investigate relationships with child health outcomes. Abbreviations: EV: extracellular vesicle; PRISM: PRogramming of Intergenerational Stress Mechanisms pregnancy cohort; LSCR: Life Stressor Checklist-Revised survey; NLE: negative life event; CRISYS-R: Crisis in Family Systems-Revised survey; KEGG: Kyoto Encyclopaedia of Genes and Genomes; NYC: New York City; SD: standard deviation; IQR: interquartile range; Cq: relative cycle threshold values; PCA: principal component analysis.
AB - Maternal stress is associated with adverse child health. Breast milk microRNAs encapsulated in extracellular vesicles (EVs) are involved in mother-infant biochemical communication during early-life programming. We leverage the PRogramming of Intergenerational Stress Mechanisms (PRISM) pregnancy cohort to investigate associations between maternal stress and breast milk EV-microRNAs. Lifetime stress and negative life events (NLEs) during pregnancy were assessed using the Life Stressor Checklist-Revised (LSCR) and the Crisis in Family Systems-Revised surveys, respectively. RNA was extracted from breast milk EVs (N = 80; collected 6.1 ± 5.9 weeks postnatally), and microRNAs were profiled using the TaqMan OpenArray Human miRNA panel. Associations between stress scores and detection (yes/no) of 173 microRNAs identified in 20–80% of samples were assessed using logistic regression; associations with expression levels of 205 EV-microRNAs identified in >50% of samples were assessed using linear regression. In adjusted models, detection of 60 and 44 EV-microRNAs was associated with higher LSCR and NLE scores, respectively (p < 0.05). Expression level of 8 and 17 EV-microRNAs was associated with LSCR and NLE scores, respectively, at our a priori criteria of p < 0.05 and |B regression|>0.2. Enriched KEGG pathways for microRNAs associated with stress scores included fatty acid metabolism and the Hippo signaling pathway. Maternal lifetime stress and NLEs during pregnancy were both associated with detection and expression level of breast milk EV-microRNAs, although associations with microRNA profiles differed between stress measures. Further research is needed to identify biological pathways impacted by associated microRNAs and investigate relationships with child health outcomes. Abbreviations: EV: extracellular vesicle; PRISM: PRogramming of Intergenerational Stress Mechanisms pregnancy cohort; LSCR: Life Stressor Checklist-Revised survey; NLE: negative life event; CRISYS-R: Crisis in Family Systems-Revised survey; KEGG: Kyoto Encyclopaedia of Genes and Genomes; NYC: New York City; SD: standard deviation; IQR: interquartile range; Cq: relative cycle threshold values; PCA: principal component analysis.
KW - Breast milk
KW - extracellular vesicles
KW - microRNA
KW - negative life events
KW - stress
UR - http://www.scopus.com/inward/record.url?scp=85089857914&partnerID=8YFLogxK
U2 - 10.1080/15592294.2020.1805677
DO - 10.1080/15592294.2020.1805677
M3 - Article
C2 - 32777999
AN - SCOPUS:85089857914
SN - 1559-2294
VL - 16
SP - 389
EP - 404
JO - Epigenetics
JF - Epigenetics
IS - 4
ER -