Neonatal Methylation and Social-Emotional Development at 6 and 18 Months of Age.

Front Behav Neurosci

Cincinnati Children's Hospital Medical Center, Department of Pediatrics, Division of Biostatistics and Epidemiology, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Published: February 2019

The variation in childhood social-emotional development within at-risk populations may be attributed in part to epigenetic mechanisms such as DNA methylation (DNAm) that respond to environmental stressors. These mechanisms may partially underlie the degree of vulnerability (and resilience) to negative social-emotional development within adverse psychosocial environments. Extensive research supports an association between maternal adversity and offspring DNAm of the gene, which encodes the glucocorticoid receptor (GR). A gap in knowledge remains regarding the relationship between DNAm, measured in neonatal (1-month of age) buccal cells, and subsequent social-emotional development during infancy and early childhood. We conducted a longitudinal cohort study of = 53 mother-child dyads ( = 30 with developmental outcomes formed the basis of current study) who were enrolled in a home visiting (HV) program. Higher mean DNAm of the exon 1 promoter was significantly associated with lower 6-month Ages and Stages Questionnaire: Social-Emotional (ASQ:SE) scores-more positive infant social-emotional functioning. A similar trend was observed at 18-months of age in a smaller sample ( = 12). The findings of this pilot study indicate that in a diverse and disadvantaged population, the level of neonatal DNAm is related to later social-emotional development. Limitations and implications for future research are discussed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371639PMC
http://dx.doi.org/10.3389/fnbeh.2019.00014DOI Listing

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