Biomarker Investigation Using Multiple Brain Measures from MRI Through Explainable Artificial Intelligence in Alzheimer's Disease Classification

被引:1
|
作者
Coluzzi, Davide [1 ,2 ]
Bordin, Valentina [1 ]
Rivolta, Massimo W. [2 ]
Fortel, Igor [3 ]
Zhan, Liang [4 ]
Leow, Alex [3 ,5 ,6 ]
Baselli, Giuseppe [1 ]
机构
[1] Politecn Milan, Dipartimento Elettron Informaz & Bioingn, I-20133 Milan, Italy
[2] Univ Milan, Dipartimento Informat, I-20133 Milan, Italy
[3] Univ Illinois, Dept Biomed Engn, Chicago, IL 60612 USA
[4] Univ Pittsburgh, Dept Elect & Comp Engn, Pittsburgh, PA 15260 USA
[5] Univ Illinois, Dept Psychiat, Chicago, IL 60612 USA
[6] Univ Illinois, Dept Comp Sci, Chicago, IL 60612 USA
来源
BIOENGINEERING-BASEL | 2025年 / 12卷 / 01期
关键词
explainable artificial intelligence; Alzheimer's disease; magnetic resonance imaging; structural connectivity; neuroimaging biomarkers;
D O I
10.3390/bioengineering12010082
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
As the leading cause of dementia worldwide, Alzheimer's Disease (AD) has prompted significant interest in developing Deep Learning (DL) approaches for its classification. However, it currently remains unclear whether these models rely on established biological indicators. This work compares a novel DL model using structural connectivity (namely, BC-GCN-SE adapted from functional connectivity tasks) with an established model using structural magnetic resonance imaging (MRI) scans (namely, ResNet18). Unlike most studies primarily focusing on performance, our work places explainability at the forefront. Specifically, we define a novel Explainable Artificial Intelligence (XAI) metric, based on gradient-weighted class activation mapping. Its aim is quantitatively measuring how effectively these models fare against established AD biomarkers in their decision-making. The XAI assessment was conducted across 132 brain parcels. Results were compared to AD-relevant regions to measure adherence to domain knowledge. Then, differences in explainability patterns between the two models were assessed to explore the insights offered by each piece of data (i.e., MRI vs. connectivity). Classification performance was satisfactory in terms of both the median true positive (ResNet18: 0.817, BC-GCN-SE: 0.703) and true negative rates (ResNet18: 0.816; BC-GCN-SE: 0.738). Statistical tests (p < 0.05) and ranking of the 15% most relevant parcels revealed the involvement of target areas: the medial temporal lobe for ResNet18 and the default mode network for BC-GCN-SE. Additionally, our findings suggest that different imaging modalities provide complementary information to DL models. This lays the foundation for bioengineering advancements in developing more comprehensive and trustworthy DL models, potentially enhancing their applicability as diagnostic support tools for neurodegenerative diseases.
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页数:28
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