自闭症谱系障碍儿童脑功能网络的个体间异质性。

IF 6.3 1区 医学 Q1 GENETICS & HEREDITY
Xiaonan Guo, Guangjin Zhai, Junfeng Liu, Yabo Cao, Xia Zhang, Dong Cui, Le Gao
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引用次数: 4

摘要

背景:自闭症谱系障碍(ASD)是一种具有相当临床异质性的神经发育障碍。本研究旨在通过脑功能网络的个体间异质性来探讨自闭症谱系障碍的异质性。方法:本研究使用来自自闭症脑成像数据交换数据库的静息状态功能磁共振成像数据,对105名ASD儿童和102名人口统计学匹配的典型对照(TC)儿童进行研究。首先获得ASD组和TC组的功能连通性(FC)网络,然后计算每个ASD个体与TC组的功能连通性(IDFC)的个体间偏差。基于IDFC模式,采用k-means聚类算法获得ASD亚型。进一步从脑区、网络和全脑水平比较ASD亚型和TC组之间的FC模式。采用支持向量回归模型分析IDFC与ASD亚型临床症状严重程度的关系。结果:根据IDFC模式确定了两种ASD亚型。与TC组相比,ASD亚型1组表现为低连接模式,ASD亚型2组表现为超连接模式。发现ASD亚型1和亚型2的IDFC分别预测ASD中社交交流障碍的严重程度和限制性行为和重复性行为的严重程度。局限性:本研究只选择了男性儿童,这限制了研究性别和发育对ASD异质性影响的能力。结论:这些结果提示ASD中存在不同FC模式的亚型,为ASD临床表现复杂的病理生理机制提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Inter-individual heterogeneity of functional brain networks in children with autism spectrum disorder.

Inter-individual heterogeneity of functional brain networks in children with autism spectrum disorder.

Inter-individual heterogeneity of functional brain networks in children with autism spectrum disorder.

Inter-individual heterogeneity of functional brain networks in children with autism spectrum disorder.

Background: Autism spectrum disorder (ASD) is a neurodevelopmental disorder with considerable clinical heterogeneity. This study aimed to explore the heterogeneity of ASD based on inter-individual heterogeneity of functional brain networks.

Methods: Resting-state functional magnetic resonance imaging data from the Autism Brain Imaging Data Exchange database were used in this study for 105 children with ASD and 102 demographically matched typical controls (TC) children. Functional connectivity (FC) networks were first obtained for ASD and TC groups, and inter-individual deviation of functional connectivity (IDFC) from the TC group was then calculated for each individual with ASD. A k-means clustering algorithm was used to obtain ASD subtypes based on IDFC patterns. The FC patterns were further compared between ASD subtypes and the TC group from the brain region, network, and whole-brain levels. The relationship between IDFC and the severity of clinical symptoms of ASD for ASD subtypes was also analyzed using a support vector regression model.

Results: Two ASD subtypes were identified based on the IDFC patterns. Compared with the TC group, the ASD subtype 1 group exhibited a hypoconnectivity pattern and the ASD subtype 2 group exhibited a hyperconnectivity pattern. IDFC for ASD subtype 1 and subtype 2 was found to predict the severity of social communication impairments and the severity of restricted and repetitive behaviors in ASD, respectively.

Limitations: Only male children were selected for this study, which limits the ability to study the effects of gender and development on ASD heterogeneity.

Conclusions: These results suggest the existence of subtypes with different FC patterns in ASD and provide insight into the complex pathophysiological mechanism of clinical manifestations of ASD.

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来源期刊
Molecular Autism
Molecular Autism GENETICS & HEREDITY-NEUROSCIENCES
CiteScore
12.10
自引率
1.60%
发文量
44
审稿时长
17 weeks
期刊介绍: Molecular Autism is a peer-reviewed, open access journal that publishes high-quality basic, translational and clinical research that has relevance to the etiology, pathobiology, or treatment of autism and related neurodevelopmental conditions. Research that includes integration across levels is encouraged. Molecular Autism publishes empirical studies, reviews, and brief communications.
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