TY - JOUR
T1 - Signed graph representation learning for functional-to-structural brain network mapping
AU - Tang, Haoteng
AU - Guo, Lei
AU - Fu, Xiyao
AU - Wang, Yalin
AU - Mackin, Scott
AU - Ajilore, Olusola
AU - Leow, Alex D.
AU - Thompson, Paul M.
AU - Huang, Heng
AU - Zhan, Liang
N1 - Funding Information:
Part of the work used the Extreme Science and Engineering Discovery Environment (XSEDE), which is supported by National Science Foundation, USA grant number ACI-1548562 . Specifically, it used the Bridges system, which is supported by NSF award number ACI-1445606 , at the Pittsburgh Supercomputing Center (PSC).
Funding Information:
Data were provided [in part] by the Human Connectome Project, MGH-USC Consortium (Principal Investigators: Bruce R. Rosen, Arthur W. Toga and Van Wedeen; U01MH093765 ) funded by the NIH Blueprint Initiative for Neuroscience Research grant ; the National Institutes of Health, USA grant P41EB015896 , and the Instrumentation Grants S10RR023043 , 1S10RR023401 , 1S10RR019307 .
Funding Information:
This study is partially supported by The National Institutes of Health, USA ( R01AG071243 , R01MH125928 and U01AG068057 ) and National Science Foundation, USA ( IIS 2045848 and IIS 1837956 ).
Funding Information:
This study is partially supported by The National Institutes of Health, USA (R01AG071243, R01MH125928 and U01AG068057) and National Science Foundation, USA (IIS 2045848 and IIS 1837956). Data were provided [in part] by the Human Connectome Project, MGH-USC Consortium (Principal Investigators: Bruce R. Rosen, Arthur W. Toga and Van Wedeen; U01MH093765) funded by the NIH Blueprint Initiative for Neuroscience Research grant; the National Institutes of Health, USA grant P41EB015896, and the Instrumentation Grants S10RR023043, 1S10RR023401, 1S10RR019307. Data were provided [in part] by OASIS-3: Longitudinal Multimodal Neuroimaging: Principal Investigators: T. Benzinger, D. Marcus, J. Morris; NIH P30 AG066444, P50 AG00561, P30 NS09857781, P01 AG026276, P01 AG003991, R01 AG043434, UL1 TR000448, R01 EB009352. AV-45 doses were provided by Avid Radiopharmaceuticals, a wholly owned subsidiary of Eli Lilly. Part of the work used the Extreme Science and Engineering Discovery Environment (XSEDE), which is supported by National Science Foundation, USA grant number ACI-1548562. Specifically, it used the Bridges system, which is supported by NSF award number ACI-1445606, at the Pittsburgh Supercomputing Center (PSC).
Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2023/1
Y1 - 2023/1
N2 - 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 perspectives, 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.
AB - 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 perspectives, 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.
KW - Functional network
KW - Multimodal
KW - Prediction
KW - Reconstruction
KW - Signed graph learning
KW - Structural network
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U2 - 10.1016/j.media.2022.102674
DO - 10.1016/j.media.2022.102674
M3 - Article
C2 - 36442294
AN - SCOPUS:85142758577
SN - 1361-8415
VL - 83
JO - Medical Image Analysis
JF - Medical Image Analysis
M1 - 102674
ER -