Gang-Qiang Han , Siu-Ching Kat , Hui Wang , Yu-Lu Yang , Zeng-Hui Ma , Ting-Ni Yin , Ya-Jing Sun , Xin-Zhou Tang , Xiao-Yun Gong , Duo Wang , Lei Li , Bing-Xi Sun , Li-Yang Zhao , Xing Su , Jia-Lu Chen , Xiao Chen , Han-Lin Wang , Xue-Ying Li , Hai-Long Liu , Xue Li , Jing Liu
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引用次数: 0
Abstract
Social skills training (SST) has demonstrated efficacy in improving social deficits in individuals with autism spectrum disorder (ASD), but the underlying neural mechanisms remain unclear. This study investigated alterations in whole-brain white matter network topology after SST in ASD individuals and explored potential correlation with improvements in social interaction deficits. 38 ASD patients aged 12 - 30 years were recruited, including 19 who completed magnetic resonance imaging (MRI) scans and social responsiveness scale (SRS) assessments at both baseline and the endpoint of a 14-week SST (training group) and 19 age-, sex-, and IQ-matched patients who underwent MRI scans and SRS assessment at the same time points but did not receive SST (control group). White matter connectivity matrices were constructed using diffusion tensor imaging (DTI), and graph theory analysis was used to assess global and nodal network properties. Paired t-tests and independent-samples t-tests were used for within- and between-group comparisons, respectively. Pearson's partial correlation was used to examine associations between network changes and SRS scores changes. After SST, four edges showed significant changes in white matter connectivity (FDR-corrected), with three increased and one decreased in the training group. Changes in nodal betweenness were also observed. While SRS scores significantly decreased in the training group, no significant correlations were found between neuroimaging changes and behavioral improvements, possibly due to the limited sample size. These findings suggest that SST may reshape white matter network, offering insights into its neural mechanisms and informing novel ASD intervention strategies.
期刊介绍:
The Brain Research Bulletin (BRB) aims to publish novel work that advances our knowledge of molecular and cellular mechanisms that underlie neural network properties associated with behavior, cognition and other brain functions during neurodevelopment and in the adult. Although clinical research is out of the Journal''s scope, the BRB also aims to publish translation research that provides insight into biological mechanisms and processes associated with neurodegeneration mechanisms, neurological diseases and neuropsychiatric disorders. The Journal is especially interested in research using novel methodologies, such as optogenetics, multielectrode array recordings and life imaging in wild-type and genetically-modified animal models, with the goal to advance our understanding of how neurons, glia and networks function in vivo.