TY - JOUR
T1 - Strength and similarity guided group-level brain functional network construction for MCI diagnosis
AU - Zhang, Yu
AU - Zhang, Han
AU - Chen, Xiaobo
AU - Liu, Mingxia
AU - Zhu, Xiaofeng
AU - Lee, Seong Whan
AU - Shen, Dinggang
N1 - Funding Information:
This study is partially supported by NIH grants ( EB006733 , EB008374 , EB009634 , MH107815 , AG041721 , and AG042599 ). Dr. S.-W. Lee was partially supported by Institute for Information & Communications Technology Promotion ( IITP ) grant funded by the Korea government (No. 2017-0-00451 ).
Publisher Copyright:
© 2018
PY - 2019/4
Y1 - 2019/4
N2 - Sparse representation-based brain functional network modeling often results in large inter-subject variability in the network structure. This could reduce the statistical power in group comparison, or even deteriorate the generalization capability of the individualized diagnosis of brain diseases. Although group sparse representation (GSR) can alleviate such a limitation by increasing network similarity across subjects, it could, in turn, fail in providing satisfactory separability between the subjects from different groups (e.g., patients vs. controls). In this study, we propose to integrate individual functional connectivity (FC) information into the GSR-based network construction framework to achieve higher between-group separability while maintaining the merit of within-group consistency. Our method was based on an observation that the subjects from the same group have generally more similar FC patterns than those from different groups. To this end, we propose our new method, namely “strength and similarity guided GSR (SSGSR)” which exploits both BOLD signal temporal correlation-based “low-order” FC (LOFC) and inter-subject LOFC-profile similarity-based “high-order” FC (HOFC) as two priors to jointly guide the GSR-based network modeling. Extensive experimental comparisons are carried out, with the rs-fMRI data from mild cognitive impairment (MCI) subjects and healthy controls, between the proposed algorithm and other state-of-the-art brain network modeling approaches. Individualized MCI identification results show that our method could achieve a balance between the individually consistent brain functional network construction and the adequately maintained inter-group brain functional network distinctions, thus leading to a more accurate classification result. Our method also provides a promising and generalized solution for the future connectome-based individualized diagnosis of brain disease.
AB - Sparse representation-based brain functional network modeling often results in large inter-subject variability in the network structure. This could reduce the statistical power in group comparison, or even deteriorate the generalization capability of the individualized diagnosis of brain diseases. Although group sparse representation (GSR) can alleviate such a limitation by increasing network similarity across subjects, it could, in turn, fail in providing satisfactory separability between the subjects from different groups (e.g., patients vs. controls). In this study, we propose to integrate individual functional connectivity (FC) information into the GSR-based network construction framework to achieve higher between-group separability while maintaining the merit of within-group consistency. Our method was based on an observation that the subjects from the same group have generally more similar FC patterns than those from different groups. To this end, we propose our new method, namely “strength and similarity guided GSR (SSGSR)” which exploits both BOLD signal temporal correlation-based “low-order” FC (LOFC) and inter-subject LOFC-profile similarity-based “high-order” FC (HOFC) as two priors to jointly guide the GSR-based network modeling. Extensive experimental comparisons are carried out, with the rs-fMRI data from mild cognitive impairment (MCI) subjects and healthy controls, between the proposed algorithm and other state-of-the-art brain network modeling approaches. Individualized MCI identification results show that our method could achieve a balance between the individually consistent brain functional network construction and the adequately maintained inter-group brain functional network distinctions, thus leading to a more accurate classification result. Our method also provides a promising and generalized solution for the future connectome-based individualized diagnosis of brain disease.
KW - Alzheimers disease
KW - Brain functional network
KW - Diagnosis
KW - Functional connectivity
KW - Group sparse representation
KW - Mild cognitive impairment
KW - Resting-state functional magnetic resonance imaging (rs-fMRI)
UR - http://www.scopus.com/inward/record.url?scp=85058043635&partnerID=8YFLogxK
U2 - 10.1016/j.patcog.2018.12.001
DO - 10.1016/j.patcog.2018.12.001
M3 - Article
AN - SCOPUS:85058043635
SN - 0031-3203
VL - 88
SP - 421
EP - 430
JO - Pattern Recognition
JF - Pattern Recognition
ER -