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自闭症谱系障碍中遗传见解与神经影像学的桥接:系统评价。

Bridging Genetic Insights with Neuroimaging in Autism Spectrum Disorder-A Systematic Review.

机构信息

Departamento de Promoção da Saúde e Doenças Não Transmissíveis, Instituto Nacional de Saúde Doutor Ricardo Jorge, Avenida Padre Cruz, 1649-016 Lisboa, Portugal.

BioISI-Biosystems & Integrative Sciences Institute, Faculty of Sciences, University of Lisboa, Campo Grande, C8, 1749-016 Lisboa, Portugal.

出版信息

Int J Mol Sci. 2024 Apr 30;25(9):4938. doi: 10.3390/ijms25094938.

Abstract

Autism Spectrum Disorder (ASD) is an early onset neurodevelopmental disorder characterized by impaired social interaction and communication, and repetitive patterns of behavior. Family studies show that ASD is highly heritable, and hundreds of genes have previously been implicated in the disorder; however, the etiology is still not fully clear. Brain imaging and electroencephalography (EEG) are key techniques that study alterations in brain structure and function. Combined with genetic analysis, these techniques have the potential to help in the clarification of the neurobiological mechanisms contributing to ASD and help in defining novel therapeutic targets. To further understand what is known today regarding the impact of genetic variants in the brain alterations observed in individuals with ASD, a systematic review was carried out using Pubmed and EBSCO databases and following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. This review shows that specific genetic variants and altered patterns of gene expression in individuals with ASD may have an effect on brain circuits associated with face processing and social cognition, and contribute to excitation-inhibition imbalances and to anomalies in brain volumes.

摘要

自闭症谱系障碍(ASD)是一种早期发生的神经发育障碍,其特征为社交互动和沟通受损,以及行为的重复模式。家族研究表明,ASD 具有高度遗传性,先前已有数百个基因与该疾病有关;然而,其病因仍不完全清楚。脑成像和脑电图(EEG)是研究大脑结构和功能改变的关键技术。结合遗传分析,这些技术有可能有助于阐明导致 ASD 的神经生物学机制,并有助于确定新的治疗靶点。为了进一步了解目前已知的与 ASD 患者大脑改变相关的遗传变异的影响,我们使用 Pubmed 和 EBSCO 数据库进行了系统评价,并遵循系统评价和荟萃分析的首选报告项目(PRISMA)指南。这项综述表明,ASD 个体中特定的遗传变异和基因表达模式的改变可能会对面部处理和社会认知相关的大脑回路产生影响,并导致兴奋-抑制失衡以及大脑体积异常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e9f/11084239/824ec5008cc2/ijms-25-04938-g001.jpg

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