Schuurmans Isabel K, Mulder Rosa H, Baltramonaityte Vilte, Lahtinen Alexandra, Qiuyu Fan, Rothmann Leonardo Melo, Staginnus Marlene, Tuulari Jetro J, Burt S Alexandra, Buss Claudia, Craig Jeffrey M, Donald Kirsten A, Eriksson Johan G, Felix Janine F, Freeman Tom P, Grassi-Oliveira Rodrigo, Huels Anke, Hyde Luke W, Jones Scott A, Karlsson Hasse, Karlsson Linnea, Koen Nastassja, Lawn Will, Mitchell Colter, Monk Christopher S, Mooney Michael A, Muetzel Ryan, Nigg Joel T, Belangero Síntia Iole Nogueira, Notterman Daniel, Ong Yi Ying, O'Connor Tom, O'Donnell Kieran J, Pan Pedro Mario, Paunio Tiina, Ryabinin Peter, Saffery Richard, Salum Giovanni A, Seal Marc, Silk Tim J, Stein Dan J, Tan Ai Peng, Teh Ai Ling, Wang Dennis, Zar Heather, Walton Esther, Cecil Charlotte A M
Department of Child and Adolescent Psychiatry and Psychology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands.
Department of Psychology, University of Bath, Bath, UK.
Mol Psychiatry. 2025 Sep 6. doi: 10.1038/s41380-025-03203-w.
Epigenetic processes, such as DNA methylation, show potential as biological markers and mechanisms underlying gene-environment interplay in the prediction of mental health and other brain-based phenotypes. However, little is known about how peripheral epigenetic patterns relate to individual differences in the brain itself. An increasingly popular approach to address this is by combining epigenetic and neuroimaging data; yet, research in this area is almost entirely comprised of cross-sectional studies in adults. To bridge this gap, we established the Methylation, Imaging and NeuroDevelopment (MIND) Consortium, which aims to bring a developmental focus to the emerging field of Neuroimaging Epigenetics by (i) promoting collaborative, adequately powered developmental research via multi-cohort analyses; (ii) increasing scientific rigor through the establishment of shared pipelines and open science practices; and (iii) advancing our understanding of DNA methylation-brain dynamics at different developmental periods (from birth to emerging adulthood), by leveraging data from prospective, longitudinal pediatric studies. MIND currently integrates 16 cohorts worldwide, comprising (repeated) measures of DNA methylation in peripheral tissues (blood, buccal cells, and saliva) and neuroimaging by magnetic resonance imaging across up to five time points over a period of up to 21 years (N = 12,877; N = 10,899; N = 6074). By triangulating associations across multiple developmental time points and study types, we hope to generate new insights into the dynamic relationships between peripheral DNA methylation and the brain, and how these ultimately relate to neurodevelopmental and psychiatric phenotypes.
表观遗传过程,如DNA甲基化,在预测心理健康和其他基于大脑的表型方面,显示出作为生物标志物和基因-环境相互作用潜在机制的可能性。然而,对于外周表观遗传模式如何与大脑本身的个体差异相关,我们知之甚少。解决这一问题的一种越来越流行的方法是将表观遗传学和神经影像学数据相结合;然而,该领域的研究几乎完全由针对成年人的横断面研究组成。为了弥补这一差距,我们成立了甲基化、成像与神经发育(MIND)联盟,其目的是通过以下方式,将发展重点引入神经影像表观遗传学这一新兴领域:(i)通过多队列分析促进协作性的、有足够效力支持的发展研究;(ii)通过建立共享流程和开放科学实践来提高科学严谨性;(iii)利用前瞻性纵向儿科研究的数据,增进我们对不同发育时期(从出生到成年初期)DNA甲基化与大脑动态关系的理解。MIND目前整合了全球16个队列,包括外周组织(血液、颊细胞和唾液)中DNA甲基化的(重复)测量数据,以及在长达21年的时间里,通过磁共振成像进行的多达五个时间点的神经影像数据(N = 12877;N = 10899;N = 6074)。通过对多个发育时间点和研究类型之间的关联进行三角测量,我们希望能够对外周DNA甲基化与大脑之间的动态关系,以及这些关系最终如何与神经发育和精神疾病表型相关,产生新的见解。