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DOI 10.1038/s41598-024-70165-4

Медицинская библиотека · Scientific reports · 2024

Enhancing early Parkinson's disease detection through multimodal deep learning and explainable AI: insights from the PPMI database.

Dentamaro Vincenzo, Impedovo Donato, Musti Luca, Pirlo Giuseppe, Taurisano Paolo

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Аннотация

Parkinson's is the second most common neurodegenerative disease, affecting nearly 8.5M people and steadily increasing. In this research, Multimodal Deep Learning is investigated for the Prodromal stage detection of Parkinson's Disease (PD), combining different 3D architectures with the novel Excitation Network (EN) and supported by Explainable Artificial Intelligence (XAI) techniques. Utilizing data from the Parkinson's Progression Markers Initiative, this study introduces a joint co-learning approach for multimodal fusion, enabling end-to-end training of deep neural networks and facilitating the learning of complementary information from both imaging and clinical modalities. DenseNet with EN outperformed other models, showing a substantial increase in accuracy when supplemented with clinical data. XAI methods, such as Integrated Gradients for ResNet and DenseNet, and Attention Heatmaps for Vision Transformer (ViT), revealed that DenseNet focused on brain regions believed to be critical to prodromal pathophysiology, including the right temporal and left pre-frontal areas. Similarly, ViT highlighted the lateral ventricles associated with cognitive decline, indicating their potential in the Prodromal stage. These findings underscore the potential of these regions as early-stage PD biomarkers and showcase the proposed framework's efficacy in predicting subtypes of PD and aiding in early diagnosis, paving the way for innovative diagnostic tools and precision medicine.

Для цитирования: Dentamaro Vincenzo, Impedovo Donato, Musti Luca, Pirlo Giuseppe, Taurisano Paolo. Enhancing early Parkinson's disease detection through multimodal deep learning and explainable AI: insights from the PPMI database.. Scientific reports. 2024. DOI: 10.1038/s41598-024-70165-4.

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