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DMFLN: A dynamic multi-scale focus learning framework for Alzheimer's disease classification.

作者信息

Wang Jikai, Jiang Mingfeng, Zhang Wei, Li Yang, Tan Tao, Wang Yaming, Li Tie-Qiang

机构信息

The School of Computer Science and Technology, Zhejiang Sci-Tech University, Hangzhou 310018, China.

The School of Computer Science and Technology, Zhejiang Sci-Tech University, Hangzhou 310018, China.

出版信息

J Neurosci Methods. 2025 Nov;423:110541. doi: 10.1016/j.jneumeth.2025.110541. Epub 2025 Jul 31.

Abstract

BACKGROUND

Magnetic resonance imaging (MRI) of gray matter plays a crucial role in the diagnosis of Alzheimer's disease (AD). Recent advances in multiscale learning techniques have improved AD classification by capturing structural information at multiple scales. However, effectively balancing the contributions of these multiscale features remains a significant challenge.

NEW METHOD

To address this issue, we propose a Dynamic Multiscale Feature Learning Network (DMFLN) for AD classification. The framework incorporates a pyramid self-attention mechanism to capture high-level global contextual features and model long-range dependencies. Additionally, a residual wavelet transform is utilized to extract fine-grained local structural features. The DMFLN adaptively adjusts the weights of features across different scales, enabling a balanced fusion of global topological representations and local morphological details.

RESULTS

We evaluate our approach on T1-weighted MRI scans from the ADNI dataset. The proposed method achieves classification accuracies of 96.32% ± 0.51%, 94.62% ± 0.39%, and 93.07% ± 0.81% for AD vs. NC, AD vs. MCI, and NC vs. MCI tasks, respectively.

COMPARISON WITH EXISTING METHODS

Compared to state-of-the-art approaches, the DMFLN framework offers improved performance by effectively addressing the challenge of multiscale feature weighting, which is often a bottleneck in multiscale fusion-based AD classification.

CONCLUSIONS

The DMFLN framework demonstrates significant improvements in AD classification by adaptively integrating global and local structural information from gray matter. These results highlight the potential of dynamic multiscale feature learning in advancing neuroimaging-based AD diagnosis.

摘要

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