Newborn Differential DNA Methylation and Subcortical Brain Volumes as Early Signs of Severe Neurodevelopmental Delay in a South African Birth Cohort Study

• Authors: Anke Hüls, Emory University; Catherine J Wedderburn, University of Cape Town; Nynke A Groenewold, University of Cape Town; Nicole Gladish, University of British Columbia; Meaghan Jones, University of Manitoba; Nastassja Koen, University of Cape Town; Julia L MacIsaac, University of British Columbia; David TS Lin, University of British Columbia; Katia E Ramadori, University of British Columbia; Michael Epstein, Emory University; Kirsten A Donald, University of Cape Town; Michael S Kobor, University of British Columbia; Heather J Zar, University of Cape Town; Dan J Stein, University of Cape Town
• Journal Title: The World Journal of Biological Psychiatry
• Volume: Volume 23, Number 8
• Publisher: Taylor & Francis | 2022-01-12, Pages 601-612
• Type of Work: Article | Post-print: After Peer Review
• Publisher DOI: http://doi.org/10.1080/15622975.2021.2016955
• Subjects: Biology, Neuroscience; Biology, Genetics; Health Sciences, Human Development
• Keywords: Early child development; methylome-wide association study; MRI imaging data; early biomarkers; brain development

Abstract

Objectives: Early detection of neurodevelopmental delay is crucial for intervention and treatment strategies. We analyzed associations between newborn DNA methylation (DNAm), neonatal magnetic resonance imaging (MRI) neuroimaging data, and neurodevelopment. Methods: Neurodevelopment was assessed in 161 children from the South African Drakenstein Child Health Study at two years of age using the Bayley Scales of Infant and Toddler Development III. We performed an epigenome-wide association study of neurodevelopmental delay using DNAm from cord blood. Subsequently, we analyzed if associations between DNAm and neurodevelopmental delay were mediated by altered neonatal brain volumes (subset of 51 children). Results: Differential DNAm at SPTBN4 (cg26971411, Δbeta=−0.024, p-value=3.28×10−08), and two intergenic regions (chromosome 11: cg00490349, Δbeta=−0.036, p-value=3.02×10−08; chromosome 17: cg15660740, Δbeta=−0.078, p-value = 6.49 × 10−08) were significantly associated with severe neurodevelopmental delay. While these associations were not mediated by neonatal brain volume, neonatal caudate volumes were independently associated with neurodevelopmental delay, particularly in language (Δcaudate volume=165.30mm3, p=0.0443) and motor (Δcaudate volume=365.36mm3, p-value=0.0082) domains. Conclusions: Differential DNAm from cord blood and increased neonatal caudate volumes were independently associated with severe neurodevelopmental delay at two years of age. These findings suggest that neurobiological signals for severe developmental delay may be detectable in very early life.