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与青少年灰质成熟和认知发展的表观遗传学关联。

Epigenetic associations with adolescent grey matter maturation and cognitive development.

作者信息

Jensen Dawn, Chen Jiayu, Turner Jessica A, Stephen Julia M, Wang Yu-Ping, Wilson Tony W, Calhoun Vince D, Liu Jingyu

机构信息

Tri-Institutional Center for Translational Research in Neuroimaging and Data Science (TReNDS), Georgia State University, Georgia Institute of Technology, Emory University, Atlanta, GA, United States.

Neuroscience Institute, Georgia State University, Atlanta, GA, United States.

出版信息

Front Genet. 2023 Jul 17;14:1222619. doi: 10.3389/fgene.2023.1222619. eCollection 2023.

Abstract

Adolescence, a critical phase of human neurodevelopment, is marked by a tremendous reorganization of the brain and accompanied by improved cognitive performance. This development is driven in part by gene expression, which in turn is partly regulated by DNA methylation (DNAm). We collected brain imaging, cognitive assessments, and DNAm in a longitudinal cohort of approximately 200 typically developing participants, aged 9-14. This data, from three time points roughly 1 year apart, was used to explore the relationships between seven cytosine-phosphate-guanine (CpG) sites in genes highly expressed in brain tissues (, , , , , , and ), seven networks of grey matter (GM) volume change, and scores from seven cognitive tests. The demethylation of the CpGs as well as the rates of change in DNAm were significantly related to improvements in total, crystalized, and fluid cognition scores, executive function, episodic memory, and processing speed, as well as several networks of GM volume increases and decreases that highlight typical patterns of brain maturation. Our study provides a first look at the DNAm of genes involved in myelination, excitatory and inhibitory receptors, and connectivity, how they are related to the large-scale changes occurring in the brain structure as well as cognition during adolescence.

摘要

青春期是人类神经发育的关键阶段,其特点是大脑发生巨大重组,并伴随着认知能力的提升。这种发育部分由基因表达驱动,而基因表达又部分受DNA甲基化(DNAm)调控。我们在一个约200名9至14岁发育正常的参与者的纵向队列中收集了脑成像、认知评估和DNAm数据。这些来自三个大致相隔1年的时间点的数据,被用于探究脑组织中高表达基因(、、、、、、和)的七个胞嘧啶-磷酸-鸟嘌呤(CpG)位点、七个灰质(GM)体积变化网络以及七项认知测试得分之间的关系。CpG的去甲基化以及DNAm的变化率与总体认知、晶态认知和流体认知得分、执行功能、情景记忆、处理速度的改善显著相关,也与几个GM体积增减网络显著相关,这些网络突出了大脑成熟的典型模式。我们的研究首次探讨了参与髓鞘形成、兴奋性和抑制性受体以及连接性的基因的DNAm,以及它们如何与青春期大脑结构和认知中发生的大规模变化相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deed/10390095/37e49087065c/fgene-14-1222619-g001.jpg

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