Multi-Scale Time-Series Kernel-Based Learning Method for Brain Disease Diagnosis

被引:15
|
作者
Zhang, Zehua [1 ]
Ding, Jiaqi [1 ]
Xu, Junhai [1 ]
Tang, Jijun [1 ,2 ,3 ]
Guo, Fei [1 ]
机构
[1] Tianjin Univ, Coll Intelligence & Comp, Tianjin 300350, Peoples R China
[2] Tianjin Univ, Key Lab Syst Bioengn, Minist Educ, Tianjin 300350, Peoples R China
[3] Univ South Carolina, Dept Comp Sci & Engn, Columbia, SC 29208 USA
基金
中国国家自然科学基金;
关键词
Time series analysis; Probability distribution; Functional magnetic resonance imaging; Diseases; Kernel; Correlation; Brain; time-series kernel; disease diagnosis; alzheimeris disease; major depressive disorder; Jensen-Shannon divergence; FUNCTIONAL CONNECTIVITY; ALZHEIMERS-DISEASE; TOOLBOX;
D O I
10.1109/JBHI.2020.2983456
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
The functional magnetic resonance imaging (fMRI) is a noninvasive technique for studying brain activity, such as brain network analysis, neural disease automated diagnosis and so on. However, many existing methods have some drawbacks, such as limitations of graph theory, lack of global topology characteristic, local sensitivity of functional connectivity, and absence of temporal or context information. In addition to many numerical features, fMRI time series data also cover specific contextual knowledge and global fluctuation information. Here, we propose multi-scale time-series kernel-based learning model for brain disease diagnosis, based on Jensen-Shannon divergence. First, we calculate correlation value within and between brain regions over time. In addition, we extract multi-scale synergy expression probability distribution (interactional relation) between brain regions. Also, we produce state transition probability distribution (sequential relation) on single brain regions. Then, we build time-series kernel-based learning model based on Jensen-Shannon divergence to measure similarity of brain functional connectivity. Finally, we provide an efficient system to deal with brain network analysis and neural disease automated diagnosis. On Alzheimers Disease Neuroimaging Initiative (ADNI) dataset, our proposed method achieves accuracy of 0.8994 and AUC of 0.8623. On Major Depressive Disorder (MDD) dataset, our proposed method achieves accuracy of 0.9166 and AUC of 0.9263. Experiments show that our proposed method outperforms other existing excellent neural disease automated diagnosis approaches. It shows that our novel prediction method performs great accurate for identification of brain diseases as well as existing outstanding prediction tools.
引用
收藏
页码:209 / 217
页数:9
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