通过半监督机器学习揭示基于单个受试者灰质网络的三种自闭症亚型

Guomei Xu, Guohong Geng, Ankang Wang, Zhangyong Li, Zhichao Liu, Yanping Liu, Jun Hu, Wei Wang, Xinwei Li
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引用次数: 0

摘要

自闭症谱系障碍(ASD)是一种异质性的早发性神经发育疾病,其特点是社交互动和沟通能力持续受损。本研究旨在根据个体灰质脑网络划分 ASD 亚型,并从图论角度提供新的见解。在这项研究中,我们提取并归一化了单个受试者的灰质网络,并计算了每个网络的拓扑特性。我们利用异质性判别分析(HYDRA)方法,根据网络属性对所有患者进行了分型。接下来,我们探讨了 ASD 亚型在网络属性和临床指标方面的差异。我们的研究发现了三种不同的 ASD 亚型。在病例对照研究中,这些亚型表现出显著差异,尤其是在中央前回、舌回和额叶中回。在病例分析中,任何两个亚型之间在整体和结节特性上都存在明显差异。在临床上,与亚型 3 相比,亚型 1 的 VIQ 和 PIQ 较低,但与亚型 2 相比,亚型 1 在 ADOS-Communication 和 ADOS-Total 中的得分较高。这些结果突显了不同亚型的男性 ASD 患者之间不同的大脑网络特性和行为,为研究 ASD 异质性的神经机制提供了宝贵的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Three autism subtypes based on single-subject gray matter network revealed by semi-supervised machine learning.

Autism spectrum disorder (ASD) is a heterogeneous, early-onset neurodevelopmental condition characterized by persistent impairments in social interaction and communication. This study aims to delineate ASD subtypes based on individual gray matter brain networks and provide new insights from a graph theory perspective. In this study, we extracted and normalized single-subject gray matter networks and calculated each network's topological properties. The heterogeneity through discriminative analysis (HYDRA) method was utilized to subtype all patients based on network properties. Next, we explored the differences among ASD subtypes in terms of network properties and clinical measures. Our investigation identified three distinct ASD subtypes. In the case-control study, these subtypes exhibited significant differences, particularly in the precentral gyrus, lingual gyrus, and middle frontal gyrus. In the case analysis, significant differences in global and nodal properties were observed between any two subtypes. Clinically, subtype 1 showed lower VIQ and PIQ compared to subtype 3, but exhibited higher scores in ADOS-Communication and ADOS-Total compared to subtype 2. The results highlight the distinct brain network properties and behaviors among different subtypes of male patients with ASD, providing valuable insights into the neural mechanisms underlying ASD heterogeneity.

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