Deep neural network CSES-NET and multi-channel feature fusion for Alzheimer's disease diagnosis

被引:3
作者
Qiao, Jianping [1 ,4 ]
Zhang, Mowen [1 ]
Fan, Yanling [1 ]
Fang, Kunlun [1 ]
Zhao, Xiuhe [2 ]
Wang, Shengjun [2 ]
Wang, Zhishun [3 ]
机构
[1] Shandong Normal Univ, Sch Phys & Elect, Shandong Prov Key Lab Med Phys & Image Proc Techno, Jinan 250014, Peoples R China
[2] Shandong Univ, Qilu Hosp, Dept Neurol, Jinan 250012, Peoples R China
[3] Columbia Univ, Dept Psychiat, New York, NY 10032 USA
[4] Shandong Normal Univ, Sch Phys & Elect, 88 Wenhua East Rd, Jinan 250014, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Deep learning; Feature fusion; Genome-wide association study; sMRI; Alzheimer's disease; MILD COGNITIVE IMPAIRMENT; CHRONIC CIGARETTE-SMOKING; ALCOHOL; GENETICS;
D O I
10.1016/j.bspc.2023.105482
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Alzheimer's disease (AD) is an irreversible brain disease. The structural Magnetic Resonance Imaging (sMRI) has been widely used in the diagnosis of AD. However, the characteristic information from a single-mode is not comprehensive. In this paper, we proposed a Convolutional- Squeeze-Excitation-Softmax-NET (CSES-NET) deep neural network combined with multi-channel feature fusion for the diagnosis of AD. First, three kinds of features were extracted including patches based on voxel morphology, cortical features based on surface morphology, and radiomics features. Next, the residual network CSES-NET was proposed to extract the deep features from the patch images in which the features were re-scaled in the residual structure in order to fit the correlation between channels. Then, the fused features of the three channels were applied to classify AD/EMCI/LMCI/NC with the fully connected neural network. Finally, radiomics and cortical features were combined with genetic data for genome-wide association study to assess genetic variants. We performed experiments with 1539 subjects from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. The experimental results verified that the proposed method improved the effectiveness of the model by extracting nonlinear deep features and fusing the multi-channel features. In addition, the genome-wide association study identified multiple risk SNPs loci which were associated with the pathological of AD and contributed to the early prevention and control of AD.
引用
收藏
页数:12
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