TY - JOUR
T1 - Can social support during pregnancy affect maternal DNA methylation? Findings from a cohort of African-Americans
AU - Surkan, Pamela J.
AU - Hong, Xiumei
AU - Zhang, Boyang
AU - Nawa, Nobutoshi
AU - Ji, Hongkai
AU - Tang, Wan Yee
AU - Ji, Yuelong
AU - Kimmel, Mary C.
AU - Wang, Guoying
AU - Pearson, Colleen
AU - Wang, Xiaobin
N1 - Publisher Copyright:
© 2019, International Pediatric Research Foundation, Inc.
PY - 2020/7/1
Y1 - 2020/7/1
N2 - Background: While stress and the absence of social support during pregnancy have been linked to poor health outcomes, the underlying biological mechanisms are unclear. Methods: We examined whether adverse experiences during pregnancy alter DNA methylation (DNAm) in maternal epigenomes. Analyses included 250 African-American mothers from the Boston Birth Cohort. Genome-wide DNAm profiling was performed in maternal blood collected after delivery, using the Infinium HumanMethylation450 Beadchip. Linear regression models, with adjustment of pertinent covariates, were applied. Results: While self-reported maternal psychosocial lifetime stress and stress during pregnancy was not associated with DNAm alterations, we found that absence of support from the baby’s father was significantly associated with maternal DNAm changes in TOR3A, IQCB1, C7orf36, and MYH7B and that lack of support from family and friends was associated with maternal DNA hypermethylation on multiple genes, including PRDM16 and BANKL. Conclusions: This study provides intriguing results suggesting biological embedding of social support during pregnancy on maternal DNAm, warranting additional investigation, and replication.
AB - Background: While stress and the absence of social support during pregnancy have been linked to poor health outcomes, the underlying biological mechanisms are unclear. Methods: We examined whether adverse experiences during pregnancy alter DNA methylation (DNAm) in maternal epigenomes. Analyses included 250 African-American mothers from the Boston Birth Cohort. Genome-wide DNAm profiling was performed in maternal blood collected after delivery, using the Infinium HumanMethylation450 Beadchip. Linear regression models, with adjustment of pertinent covariates, were applied. Results: While self-reported maternal psychosocial lifetime stress and stress during pregnancy was not associated with DNAm alterations, we found that absence of support from the baby’s father was significantly associated with maternal DNAm changes in TOR3A, IQCB1, C7orf36, and MYH7B and that lack of support from family and friends was associated with maternal DNA hypermethylation on multiple genes, including PRDM16 and BANKL. Conclusions: This study provides intriguing results suggesting biological embedding of social support during pregnancy on maternal DNAm, warranting additional investigation, and replication.
UR - http://www.scopus.com/inward/record.url?scp=85070097191&partnerID=8YFLogxK
U2 - 10.1038/s41390-019-0512-7
DO - 10.1038/s41390-019-0512-7
M3 - Article
C2 - 31349361
AN - SCOPUS:85070097191
SN - 0031-3998
VL - 88
SP - 131
EP - 138
JO - Pediatric research
JF - Pediatric research
IS - 1
ER -