Molecular PsychiatryGenomicsPeer-reviewed journal article
Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group
Tianye JiaiD, Congying ChuiD, Yun LiuiD, Jenny van DongeniD, Evangelos Papastergios, Nicola J. ArmstrongiD, Mark E. BastiniD, Tania Carrillo‐RoaiD, Anouk den BraberiD, Mathew A. HarrisiD, Rick JanseniD, Jingyu LiuiD, Michelle Luciano AiD, Anil P. S. OriiD, Roberto Roiz‐SantiáñeziD, Barbara RuggeriiD, Daniil SarkisyaniD, Jean ShiniD, Sungeun KimiD, Diana Tordesillas‐GutiérreziD, Dennis van ‘t EntiD, David J. Ames, Eric Artiges AiD, Georgy Ya. BakalkiniD, Tobias BanaschewskiiD, , Sylvane DesrivièresiD
Abstract
DNA methylation, which is modulated by both genetic factors and environmental exposures, may offer a unique opportunity to discover novel biomarkers of disease-related brain phenotypes, even when measured in other tissues than brain, such as blood. A few studies of small sample sizes have revealed associations between blood DNA methylation and neuropsychopathology, however, large-scale epigenome-wide association studies (EWAS) are needed to investigate the utility of DNA methylation profiling as a peripheral marker for the brain. Here, in an analysis of eleven international cohorts, totalling 3,337 individuals, we report epigenome-wide meta-analyses of blood DNA methylation with volumes of the hippocampus, thalamus and nucleus accumbens (NAcc) -three subcortical regions selected for their associations with disease and heritability and volumetric variability. Analyses of individual CpGs revealed genome-wide significant associations with hippocampal volume at two loci. No significant associations were found for analyses of thalamus and nucleus accumbens volumes. CpG sites associated with hippocampus volume were significantly enriched within cancer-related genes and within regulatory elements containing the transcriptionally repressive histone H3K27 tri-methylation mark that is vital for stem cell fate specification. Cluster-based analyses revealed additional differentially methylated regions (DMRs) associated with hippocampal volume. DNA methylation at these loci affected expression of proximal genes involved in in learning and memory, stem cell maintenance and differentiation, fatty acid metabolism and type-2 diabetes. These DNA methylation marks, their interaction with genetic variants and their impact on gene expression offer new insights into the relationship between epigenetic variation and brain structure and may provide the basis for biomarker discovery in neurodegeneration and neuropsychiatric conditions.
- organism: human
- assay: DNA methylation
- research focus: differential expression
- approach: statistical model
- Citations
- 57
- FWCI
- 0.75
- Field percentile
- top 37%
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