Explaining graph convolutional network predictions for clinicians-An explainable AI approach to Alzheimer's disease classification

被引:2
|
作者
Tekkesinoglu, Sule [1 ]
Pudas, Sara [2 ,3 ]
机构
[1] Umea Univ, Dept Comp Sci, Umea, Sweden
[2] Umea Univ, Dept Integrat Med Biol IMB, Umea, Sweden
[3] Umea Univ, Umea Ctr Funct Brain Imaging, Umea, Sweden
来源
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
explainable AI; multimodal data; graph convolutional networks; Alzheimer's disease; node classification; ALZHEIMERS-DISEASE;
D O I
10.3389/frai.2023.1334613
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Introduction Graph-based representations are becoming more common in the medical domain, where each node defines a patient, and the edges signify associations between patients, relating individuals with disease and symptoms in a node classification task. In this study, a Graph Convolutional Networks (GCN) model was utilized to capture differences in neurocognitive, genetic, and brain atrophy patterns that can predict cognitive status, ranging from Normal Cognition (NC) to Mild Cognitive Impairment (MCI) and Alzheimer's Disease (AD), on the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. Elucidating model predictions is vital in medical applications to promote clinical adoption and establish physician trust. Therefore, we introduce a decomposition-based explanation method for individual patient classification.Methods Our method involves analyzing the output variations resulting from decomposing input values, which allows us to determine the degree of impact on the prediction. Through this process, we gain insight into how each feature from various modalities, both at the individual and group levels, contributes to the diagnostic result. Given that graph data contains critical information in edges, we studied relational data by silencing all the edges of a particular class, thereby obtaining explanations at the neighborhood level.Results Our functional evaluation showed that the explanations remain stable with minor changes in input values, specifically for edge weights exceeding 0.80. Additionally, our comparative analysis against SHAP values yielded comparable results with significantly reduced computational time. To further validate the model's explanations, we conducted a survey study with 11 domain experts. The majority (71%) of the responses confirmed the correctness of the explanations, with a rating of above six on a 10-point scale for the understandability of the explanations.Discussion Strategies to overcome perceived limitations, such as the GCN's overreliance on demographic information, were discussed to facilitate future adoption into clinical practice and gain clinicians' trust as a diagnostic decision support system.
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收藏
页数:20
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