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Contributions of Prenatal Risk Factors and Neonatal Epigenetics to Cognitive Outcome in Children Born Very Preterm

Title: Contributions of Prenatal Risk Factors and Neonatal Epigenetics to Cognitive Outcome in Children Born Very Preterm
Language: English
Authors: Marie Camerota (ORCID 0000-0001-8293-6467); Barry M. Lester; Elisabeth C. McGowan; Brian S. Carter; Jennifer Check; Lynne M. Dansereau; Sheri A. DellaGrotta; Jennifer B. Helderman; Julie A. Hofheimer; Cynthia M. Loncar; Charles R. Neal; T. Michael O'Shea; Steven L. Pastyrnak; Lynne M. Smith; Sarina Abrishamcar; Anke Hüls; Carmen J. Marsit; Todd M. Everson
Source: Developmental Psychology. 2024 60(9):1606-1619.
Availability: American Psychological Association. Journals Department, 750 First Street NE, Washington, DC 20002. Tel: 800-374-2721; Tel: 202-336-5510; Fax: 202-336-5502; e-mail: order@apa.org; Web site: http://www.apa.org
Peer Reviewed: Y
Page Count: 14
Publication Date: 2024
Sponsoring Agency: National Institutes of Health (NIH) (DHHS); National Institute of Mental Health (NIMH) (DHHS/NIH)
Contract Number: R01HD072267; R01HD084515
Document Type: Journal Articles; Reports - Research
Descriptors: Premature Infants; Prenatal Influences; Toddlers; Risk; Cognitive Ability; Child Development; Infants; Genetics; Risk Assessment
Assessment and Survey Identifiers: Bayley Scales of Infant and Toddler Development
DOI: 10.1037/dev0001709
ISSN: 0012-1649; 1939-0599
Abstract: Children born less than 30 weeks gestational age (GA) are at high risk for neurodevelopmental delay compared to term peers. Prenatal risk factors and neonatal epigenetics could help identify preterm children at highest risk for poor cognitive outcomes. We aimed to understand the associations among cumulative prenatal risk, neonatal DNA methylation, and child cognitive ability at age 3 years, including whether DNA methylation mediates the association between prenatal risk and cognitive ability. We studied 379 neonates (54% male) born less than 30 weeks GA who had DNA methylation measured at neonatal intensive care unit discharge along with 3-year follow-up data. Cumulative prenatal risk was calculated from 24 risk factors obtained from maternal report and medical record and epigenome-wide neonatal DNA methylation was assayed from buccal swabs. At 3-year follow-up, child cognitive ability was assessed using the "Bayley Scales of Infant and Toddler Development" (third edition). Cumulative prenatal risk and DNA methylation at two cytosine-phosphate-guanines (CpGs) were uniquely associated with child cognitive ability. Using high-dimensional mediation analysis, we also identified differential methylation of 309 CpGs that mediated the association between cumulative prenatal risk and child cognitive ability. Many of the associated CpGs were located in genes (TNS3, TRAPPC4, MAD1L1, APBB2, DIP2C, TRAPPC9, DRD2) that have previously been associated with prenatal exposures and/or neurodevelopmental phenotypes. Our findings suggest a role for both prenatal risk factors and DNA methylation in explaining outcomes for children born preterm and suggest we should further study DNA methylation as a potential mechanism underlying the association between prenatal risk and child neurodevelopment.
Abstractor: As Provided
Entry Date: 2026
Accession Number: EJ1500077
Database: ERIC