Graph convolution network with similarity awareness and adaptive calibration for disease-induced deterioration prediction

•We design a similarity-aware graph in GCN to consider disease statuses.•We propose an adaptive mechanism to estimate similarities.•We propose a calibration mechanism to fuse functional and structural information.•We obtain promising performance for disease deterioration prediction. [Display omitted...

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Published inMedical image analysis Vol. 69; p. 101947
Main Authors Song, Xuegang, Zhou, Feng, Frangi, Alejandro F, Cao, Jiuwen, Xiao, Xiaohua, Lei, Yi, Wang, Tianfu, Lei, Baiying
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.04.2021
Elsevier BV
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Online AccessGet full text
ISSN1361-8415
1361-8423
1361-8423
DOI10.1016/j.media.2020.101947

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Summary:•We design a similarity-aware graph in GCN to consider disease statuses.•We propose an adaptive mechanism to estimate similarities.•We propose a calibration mechanism to fuse functional and structural information.•We obtain promising performance for disease deterioration prediction. [Display omitted] Graph convolution networks (GCN) have been successfully applied in disease prediction tasks as they capture interactions (i.e., edges and edge weights on the graph) between individual elements. The interactions in existing works are constructed by fusing similarity between imaging information and distance between non-imaging information, whereas disregarding the disease status of those individuals in the training set. Besides, the similarity is being evaluated by computing the correlation distance between feature vectors, which limits prediction performance, especially for predicting significant memory concern (SMC) and mild cognitive impairment (MCI). In this paper, we propose three mechanisms to improve GCN, namely similarity-aware adaptive calibrated GCN (SAC-GCN), for predicting SMC and MCI. First, we design a similarity-aware graph using different receptive fields to consider disease status. The labelled subjects on the graph are only connected with those labelled subjects with the same status. Second, we propose an adaptive mechanism to evaluate similarity. Specifically, we construct initial GCN with evaluating similarity by using traditional correlation distance, then pre-train the initial GCN by using training samples and use it to score all subjects. Then, the difference between these scores replaces correlation distance to update similarity. Last, we devise a calibration mechanism to fuse functional magnetic resonance imaging (fMRI) and diffusion tensor imaging (DTI) information into edges. The proposed method is tested on the Alzheimer's Disease Neuroimaging Initiative (ADNI) dataset. Experimental results demonstrate that our proposed method is useful to predict disease-induced deterioration and superior to other related algorithms, with a mean classification accuracy of 86.83% in our prediction tasks.
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ISSN:1361-8415
1361-8423
1361-8423
DOI:10.1016/j.media.2020.101947