静态功能连通性分析的异构图表示学习框架

Guangqi Wen;Peng Cao;Lingwen Liu;Maochun Hao;Siyu Liu;Junjie Zheng;Jinzhu Yang;Osmar R. Zaiane;Fei Wang
{"title":"静态功能连通性分析的异构图表示学习框架","authors":"Guangqi Wen;Peng Cao;Lingwen Liu;Maochun Hao;Siyu Liu;Junjie Zheng;Jinzhu Yang;Osmar R. Zaiane;Fei Wang","doi":"10.1109/TMI.2024.3512603","DOIUrl":null,"url":null,"abstract":"Brain functional connectivity analysis is important for understanding brain development and brain disorders. Recent studies have suggested that the variations of functional connectivity among multiple subnetworks are closely related to the development of diseases. However, the existing works failed to sufficiently capture the complex correlation patterns among the subnetworks and ignored the learning of heterogeneous structural information across the subnetworks. To address these issues, we formulate a new paradigm for constructing and analyzing high-order heterogeneous functional brain networks via meta-paths and propose a Heterogeneous Graph representation Learning framework (BrainHGL). Our framework consists of three key aspects: 1) Meta-path encoding for capturing rich heterogeneous topological information, 2) Meta-path interaction for exploiting complex association patterns among subnetworks and 3) Meta-path aggregation for better meta-path fusion. To the best of our knowledge, we are the first to formulate the heterogeneous brain networks for better exploiting the relationship between the subnetwork interactions and the mental disease We evaluate BrainHGL on the private center Nanjing Medical University dataset (center NMU) and the public Autism Brain Imaging Data Exchange (ABIDE) dataset. We demonstrate the effectiveness of the proposed model across various disease classification tasks, including major depression disorder (MDD), bipolar disorder (BD) and autism spectrum disorder (ASD) diagnoses. In addition, our model provides deeper insights into disease interpretability, including the critical brain subnetwork connectivities, brain regions and functional pathways. We also identified disease subtypes consistent with previous neuroscientific studies by our model, which benefits the disease identification performance. The code is available at <uri>https://github.com/IntelliDAL/Graph/BrainHGL</uri>","PeriodicalId":94033,"journal":{"name":"IEEE transactions on medical imaging","volume":"44 3","pages":"1581-1595"},"PeriodicalIF":0.0000,"publicationDate":"2024-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Heterogeneous Graph Representation Learning Framework for Resting-State Functional Connectivity Analysis\",\"authors\":\"Guangqi Wen;Peng Cao;Lingwen Liu;Maochun Hao;Siyu Liu;Junjie Zheng;Jinzhu Yang;Osmar R. Zaiane;Fei Wang\",\"doi\":\"10.1109/TMI.2024.3512603\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Brain functional connectivity analysis is important for understanding brain development and brain disorders. Recent studies have suggested that the variations of functional connectivity among multiple subnetworks are closely related to the development of diseases. However, the existing works failed to sufficiently capture the complex correlation patterns among the subnetworks and ignored the learning of heterogeneous structural information across the subnetworks. To address these issues, we formulate a new paradigm for constructing and analyzing high-order heterogeneous functional brain networks via meta-paths and propose a Heterogeneous Graph representation Learning framework (BrainHGL). Our framework consists of three key aspects: 1) Meta-path encoding for capturing rich heterogeneous topological information, 2) Meta-path interaction for exploiting complex association patterns among subnetworks and 3) Meta-path aggregation for better meta-path fusion. To the best of our knowledge, we are the first to formulate the heterogeneous brain networks for better exploiting the relationship between the subnetwork interactions and the mental disease We evaluate BrainHGL on the private center Nanjing Medical University dataset (center NMU) and the public Autism Brain Imaging Data Exchange (ABIDE) dataset. We demonstrate the effectiveness of the proposed model across various disease classification tasks, including major depression disorder (MDD), bipolar disorder (BD) and autism spectrum disorder (ASD) diagnoses. In addition, our model provides deeper insights into disease interpretability, including the critical brain subnetwork connectivities, brain regions and functional pathways. We also identified disease subtypes consistent with previous neuroscientific studies by our model, which benefits the disease identification performance. The code is available at <uri>https://github.com/IntelliDAL/Graph/BrainHGL</uri>\",\"PeriodicalId\":94033,\"journal\":{\"name\":\"IEEE transactions on medical imaging\",\"volume\":\"44 3\",\"pages\":\"1581-1595\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-12-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IEEE transactions on medical imaging\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://ieeexplore.ieee.org/document/10781429/\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE transactions on medical imaging","FirstCategoryId":"1085","ListUrlMain":"https://ieeexplore.ieee.org/document/10781429/","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

脑功能连通性分析对于理解大脑发育和大脑疾病具有重要意义。最近的研究表明,多个子网络之间功能连接的变化与疾病的发展密切相关。然而,现有的工作未能充分捕获子网之间复杂的关联模式,忽略了跨子网异构结构信息的学习。为了解决这些问题,我们制定了一个新的范式,通过元路径构建和分析高阶异构功能脑网络,并提出了一个异构图表示学习框架(BrainHGL)。我们的框架包括三个关键方面:1)元路径编码,用于捕获丰富的异构拓扑信息;2)元路径交互,用于利用子网之间复杂的关联模式;3)元路径聚合,用于更好的元路径融合。据我们所知,我们是第一个制定异构脑网络,以更好地利用子网相互作用与精神疾病之间的关系。我们在私立中心南京医科大学数据集(中心NMU)和公共自闭症脑成像数据交换(ABIDE)数据集上评估BrainHGL。我们证明了该模型在各种疾病分类任务中的有效性,包括重度抑郁症(MDD)、双相情感障碍(BD)和自闭症谱系障碍(ASD)诊断。此外,我们的模型提供了对疾病可解释性的更深入的见解,包括关键的大脑子网连接,大脑区域和功能途径。我们还通过我们的模型确定了与先前神经科学研究一致的疾病亚型,这有利于疾病识别性能。代码可在https://github.com/IntelliDAL/Graph/BrainHGL上获得
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Heterogeneous Graph Representation Learning Framework for Resting-State Functional Connectivity Analysis
Brain functional connectivity analysis is important for understanding brain development and brain disorders. Recent studies have suggested that the variations of functional connectivity among multiple subnetworks are closely related to the development of diseases. However, the existing works failed to sufficiently capture the complex correlation patterns among the subnetworks and ignored the learning of heterogeneous structural information across the subnetworks. To address these issues, we formulate a new paradigm for constructing and analyzing high-order heterogeneous functional brain networks via meta-paths and propose a Heterogeneous Graph representation Learning framework (BrainHGL). Our framework consists of three key aspects: 1) Meta-path encoding for capturing rich heterogeneous topological information, 2) Meta-path interaction for exploiting complex association patterns among subnetworks and 3) Meta-path aggregation for better meta-path fusion. To the best of our knowledge, we are the first to formulate the heterogeneous brain networks for better exploiting the relationship between the subnetwork interactions and the mental disease We evaluate BrainHGL on the private center Nanjing Medical University dataset (center NMU) and the public Autism Brain Imaging Data Exchange (ABIDE) dataset. We demonstrate the effectiveness of the proposed model across various disease classification tasks, including major depression disorder (MDD), bipolar disorder (BD) and autism spectrum disorder (ASD) diagnoses. In addition, our model provides deeper insights into disease interpretability, including the critical brain subnetwork connectivities, brain regions and functional pathways. We also identified disease subtypes consistent with previous neuroscientific studies by our model, which benefits the disease identification performance. The code is available at https://github.com/IntelliDAL/Graph/BrainHGL
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信