{"title":"mGNN-bw:基于有偏随机漫步路径聚合的多尺度图神经网络用于 ASD 诊断","authors":"Wenqiu Pan;Guang Ling;Feng Liu","doi":"10.1109/TNSRE.2025.3543177","DOIUrl":null,"url":null,"abstract":"In recent years, computationally assisted diagnosis for classifying autism spectrum disorder (ASD) and typically developing (TD) individuals based on neuroimaging data, such as functional magnetic resonance imaging (fMRI), has garnered significant attention. Studies have shown that long-range functional connectivity patterns in ASD patients exhibit significant abnormalities, and individual brain networks display considerable heterogeneity. However, current graph neural networks (GNNs) used in ASD research have failed to adequately capture long-range connectivity and have overlooked individual differences. To address these limitations, this study proposes a novel multi-scale graph neural network based on biased random walks (mGNN-bw). The model introduces a co-optimization strategy between sub-models and the main model, leveraging node pooling scores from sub-models to guide biased random walks, effectively capturing long-range connectivity. By constructing high-order brain networks through path encoding and aggregation, and integrating them with low-order brain networks based on Pearson correlation, the model achieves a robust multi-scale feature representation. Experimental results on the publicly available ABIDE I dataset demonstrate the superior performance of our approach, achieving accuracy rates of 74.8% and 73.2% using CC200 and AAL atlases, respectively, outperforming existing methods. Additionally, the model identifies key ASD-associated brain regions, including the frontal lobe, insula, cingulate, and calcarine, supported by existing research. The proposed method significantly contributes to the clinical diagnosis of ASD.","PeriodicalId":13419,"journal":{"name":"IEEE Transactions on Neural Systems and Rehabilitation Engineering","volume":"33 ","pages":"900-910"},"PeriodicalIF":4.8000,"publicationDate":"2025-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=10896757","citationCount":"0","resultStr":"{\"title\":\"mGNN-bw: Multi-Scale Graph Neural Network Based on Biased Random Walk Path Aggregation for ASD Diagnosis\",\"authors\":\"Wenqiu Pan;Guang Ling;Feng Liu\",\"doi\":\"10.1109/TNSRE.2025.3543177\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In recent years, computationally assisted diagnosis for classifying autism spectrum disorder (ASD) and typically developing (TD) individuals based on neuroimaging data, such as functional magnetic resonance imaging (fMRI), has garnered significant attention. Studies have shown that long-range functional connectivity patterns in ASD patients exhibit significant abnormalities, and individual brain networks display considerable heterogeneity. However, current graph neural networks (GNNs) used in ASD research have failed to adequately capture long-range connectivity and have overlooked individual differences. To address these limitations, this study proposes a novel multi-scale graph neural network based on biased random walks (mGNN-bw). The model introduces a co-optimization strategy between sub-models and the main model, leveraging node pooling scores from sub-models to guide biased random walks, effectively capturing long-range connectivity. By constructing high-order brain networks through path encoding and aggregation, and integrating them with low-order brain networks based on Pearson correlation, the model achieves a robust multi-scale feature representation. Experimental results on the publicly available ABIDE I dataset demonstrate the superior performance of our approach, achieving accuracy rates of 74.8% and 73.2% using CC200 and AAL atlases, respectively, outperforming existing methods. Additionally, the model identifies key ASD-associated brain regions, including the frontal lobe, insula, cingulate, and calcarine, supported by existing research. The proposed method significantly contributes to the clinical diagnosis of ASD.\",\"PeriodicalId\":13419,\"journal\":{\"name\":\"IEEE Transactions on Neural Systems and Rehabilitation Engineering\",\"volume\":\"33 \",\"pages\":\"900-910\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2025-02-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=10896757\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IEEE Transactions on Neural Systems and Rehabilitation Engineering\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://ieeexplore.ieee.org/document/10896757/\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENGINEERING, BIOMEDICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE Transactions on Neural Systems and Rehabilitation Engineering","FirstCategoryId":"5","ListUrlMain":"https://ieeexplore.ieee.org/document/10896757/","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
mGNN-bw: Multi-Scale Graph Neural Network Based on Biased Random Walk Path Aggregation for ASD Diagnosis
In recent years, computationally assisted diagnosis for classifying autism spectrum disorder (ASD) and typically developing (TD) individuals based on neuroimaging data, such as functional magnetic resonance imaging (fMRI), has garnered significant attention. Studies have shown that long-range functional connectivity patterns in ASD patients exhibit significant abnormalities, and individual brain networks display considerable heterogeneity. However, current graph neural networks (GNNs) used in ASD research have failed to adequately capture long-range connectivity and have overlooked individual differences. To address these limitations, this study proposes a novel multi-scale graph neural network based on biased random walks (mGNN-bw). The model introduces a co-optimization strategy between sub-models and the main model, leveraging node pooling scores from sub-models to guide biased random walks, effectively capturing long-range connectivity. By constructing high-order brain networks through path encoding and aggregation, and integrating them with low-order brain networks based on Pearson correlation, the model achieves a robust multi-scale feature representation. Experimental results on the publicly available ABIDE I dataset demonstrate the superior performance of our approach, achieving accuracy rates of 74.8% and 73.2% using CC200 and AAL atlases, respectively, outperforming existing methods. Additionally, the model identifies key ASD-associated brain regions, including the frontal lobe, insula, cingulate, and calcarine, supported by existing research. The proposed method significantly contributes to the clinical diagnosis of ASD.
期刊介绍:
Rehabilitative and neural aspects of biomedical engineering, including functional electrical stimulation, acoustic dynamics, human performance measurement and analysis, nerve stimulation, electromyography, motor control and stimulation; and hardware and software applications for rehabilitation engineering and assistive devices.