Signed graph representation learning for functional-to-structural brain network mapping

被引:10
|
作者
Tang, Haoteng [1 ]
Guo, Lei [1 ]
Fu, Xiyao [1 ]
Wang, Yalin [4 ]
Mackin, Scott [5 ]
Ajilore, Olusola [3 ]
Leow, Alex D. [3 ]
Thompson, Paul M. [2 ]
Huang, Heng [1 ]
Zhan, Liang [1 ]
机构
[1] Univ Pittsburgh, 3700 OHara St, Pittsburgh, PA 15261 USA
[2] Univ Southern Calif, 2001 N Soto St, Los Angeles, CA 90032 USA
[3] Univ Illinois, 1601 W Taylor St, Chicago, IL 60612 USA
[4] Arizona State Univ, 699 S Mill Ave, Tempe, AZ 85281 USA
[5] Univ Calif San Francisco, 505 Parnassus Ave, San Francisco, CA 94143 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Signed graph learning; Multimodal; Structural network; Functional network; Reconstruction; Prediction; CONNECTIVITY; PARCELLATION; BALANCE;
D O I
10.1016/j.media.2022.102674
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
MRI-derived brain networks have been widely used to understand functional and structural interactions among brain regions, and factors that affect them, such as brain development and diseases. Graph mining on brain networks can facilitate the discovery of novel biomarkers for clinical phenotypes and neurodegenerative diseases. Since brain functional and structural networks describe the brain topology from different perspec-tives, exploring a representation that combines these cross-modality brain networks has significant clinical implications. Most current studies aim to extract a fused representation by projecting the structural network to the functional counterpart. Since the functional network is dynamic and the structural network is static, mapping a static object to a dynamic object may not be optimal. However, mapping in the opposite direction (i.e., from functional to structural networks) are suffered from the challenges introduced by negative links within signed graphs. Here, we propose a novel graph learning framework, named as Deep Signed Brain Graph Mining or DSBGM, with a signed graph encoder that, from an opposite perspective, learns the cross-modality representations by projecting the functional network to the structural counterpart. We validate our framework on clinical phenotype and neurodegenerative disease prediction tasks using two independent, publicly available datasets (HCP and OASIS). Our experimental results clearly demonstrate the advantages of our model compared to several state-of-the-art methods.
引用
收藏
页数:9
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