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塑造精神分裂症脑改变的跨尺度特性:磁共振成像与编码及非编码区域单核苷酸多态性研究

Shaping the Trans-Scale Properties of Schizophrenia Cerebral Alterations on Magnetic Resonance Imaging and Single-Nucleotide Polymorphisms of Coding and Non-Coding Regions.

作者信息

Zhao Shu-Wan, Xu Xian, Wang Xian-Yang, Yan Tian-Cai, Cao Yang, Yan Qing-Hong, Chen Kun, Jin Yin-Chuan, Zhang Ya-Hong, Yin Hong, Cui Long-Biao

机构信息

Department of Clinical Psychology, School of Medical Psychology, Fourth Military Medical University, Xi'an, China.

Department of Radiology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.

出版信息

Front Hum Neurosci. 2021 Sep 9;15:720239. doi: 10.3389/fnhum.2021.720239. eCollection 2021.

DOI:10.3389/fnhum.2021.720239
PMID:34566604
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8458928/
Abstract

Schizophrenia is a complex mental illness with genetic heterogeneity, which is often accompanied by alterations in brain structure and function. The neurobiological mechanism of schizophrenia associated with heredity remains unknown. Recently, the development of trans-scale and multi-omics methods that integrate gene and imaging information sheds new light on the nature of schizophrenia. In this article, we summarized the results of brain structural and functional changes related to the specific single-nucleotide polymorphisms (SNPs) in the past decade, and the SNPs were divided into non-coding regions and coding regions, respectively. It is hoped that the relationship between SNPs and cerebral alterations can be displayed more clearly and intuitively, so as to provide fresh approaches for the discovery of potential biomarkers and the development of clinical accurate individualized treatment decision-making.

摘要

精神分裂症是一种具有遗传异质性的复杂精神疾病,常伴有脑结构和功能的改变。与遗传相关的精神分裂症神经生物学机制尚不清楚。近年来,整合基因和影像信息的跨尺度多组学方法的发展为精神分裂症的本质研究带来了新的启示。本文总结了过去十年中与特定单核苷酸多态性(SNP)相关的脑结构和功能变化结果,这些SNP分别分为非编码区和编码区。希望能更清晰直观地展示SNP与脑改变之间的关系,为发现潜在生物标志物和制定临床精准个体化治疗决策提供新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2066/8458928/0e8eab6c7937/fnhum-15-720239-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2066/8458928/0e8eab6c7937/fnhum-15-720239-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2066/8458928/0e8eab6c7937/fnhum-15-720239-g0001.jpg

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本文引用的文献

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Integrative omics of schizophrenia: from genetic determinants to clinical classification and risk prediction.精神分裂症的综合组学:从遗传决定因素到临床分类和风险预测。
Mol Psychiatry. 2022 Jan;27(1):113-126. doi: 10.1038/s41380-021-01201-2. Epub 2021 Jun 30.
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Modulation on Glutamic Pathway of Frontal-Striatum-Thalamus by rs11146020 and rs3813296 Gene Polymorphism in First-Episode Negative Schizophrenia.首发阴性精神分裂症中rs11146020和rs3813296基因多态性对额-纹状体-丘脑谷氨酸通路的调控作用
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A neuroimaging biomarker for striatal dysfunction in schizophrenia.精神分裂症纹状体功能障碍的神经影像学生物标志物。
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Integrating Clinical Data and Imputed Transcriptome from GWAS to Uncover Complex Disease Subtypes: Applications in Psychiatry and Cardiology.整合 GWAS 的临床数据和推断转录组,揭示复杂疾病亚型:在精神病学和心脏病学中的应用。
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Association of rs1059004 polymorphism in the OLIG2 locus with whole-brain functional connectivity in first-episode schizophrenia.OLIG2 基因座 rs1059004 多态性与首发精神分裂症全脑功能连接的关联。
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Single nucleotide polymorphisms in piRNA-pathway genes: an insight into genetic determinants of human diseases.piRNA 通路基因中的单核苷酸多态性:人类疾病遗传决定因素的新视角。
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