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Epigenome-wide meta-analyses of blood DNA methylation and its association with subcortical volumes: Findings from the ENIGMA Epigenetics Working Group

Research output: Contribution to journalArticle

  • Tianye Jia
  • Congying Chu
  • Yun Liu
  • Jenny van Dongen
  • Evangelous Papastergios
  • Nicola J Armstrong
  • Tania Carrillo-roa
  • Anouk den Braber
  • Rick Jansen
  • Jingyu Liu
  • Anil P. S. Ori
  • Roberto Roiz-Santianez
  • Barbara Ruggeri
  • Daniil Sarkisyan
  • Jean Shin
  • Kim Sungeun
  • Diana Tordesillas-Gutierrez
  • Dennis Van't Ent
  • David Ames
  • Eric Artiges
  • Georgy Bakalkin
  • Tobias Banaschewski
  • Arun L W Bokde
  • Henry Brodaty
  • Uli Bromberg
  • Rachel M Brouwer
  • Christian Büchel
  • Erin B. Quinlan
  • Wiepke Cahn
  • Greig I de Zubicaray
  • Stefan Ehrlich
  • Tomas J Ekström
  • Herta Flor
  • Juliane H Fröhner
  • Vincent Frouin
  • Hugh Garavan
  • Penny A Gowland
  • Andreas Heinz
  • Jacqueline Hoare
  • Bernd Ittermann
  • Neda Jahanshad
  • Jiyang Jiang
  • John B J Kwok
  • Nicholas G Martin
  • Jean-Luc Martinot
  • Karen A Mather
  • Katie L McMahon
  • Allan F. Mcrae
  • Frauke Nees
  • Dimitri Papadopoulos Orfanos
  • Tomas Paus
  • Luise Poustka
  • Philipp G Sämann
  • Peter R Schofield
  • Michael N Smolka
  • Dan J Stein
  • Lachlan T Strike
  • Jalmar Teeuw
  • Anbupalam Thalamuthu
  • Julian N. Trollor
  • Henrik Walter
  • Wei Wen
  • Robert Whelan
  • Liana G Apostolova
  • Elisabeth B. Binder
  • Dorrett Boomsma
  • Vince D Calhoun
  • Benedicto Crespo-Facorro
  • Hilleke E. Hulshoff Pol
  • Roel A. Ophoff
  • Zdenka Pausova
  • Perminder S Sachdev
  • Andrew J Saykin
  • Margaret J Wright
  • Paul M. Thompson
  • Gunter Schumann
  • Sylvane Desrivières

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Original languageEnglish
JournalMolecular Psychiatry
Early online date6 Dec 2019
DOIs
Publication statusE-pub ahead of print - 6 Dec 2019

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. 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 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.

    Research areas

  • genetics, molecular biology

ID: 120563118