ADNP-15: An Open-Source Histopathological Dataset for Neuritic Plaque Segmentation in Human Brain Whole Slide Images with Frequency Domain Image Enhancement for Stain Normalization

Alzheimer's Disease (AD) is a neurodegenerative disorder characterized by amyloid-beta plaques and tau neurofibrillary tangles, which serve as key histopathological features. The identification and segmentation of these lesions are crucial for understanding AD progression but remain challenging due to the lack of large-scale annotated datasets and the impact of staining variations on automated image analysis. Deep learning has emerged as a powerful tool for pathology image segmentation; however, model performance is significantly influenced by variations in staining characteristics, necessitating effective stain normalization and enhancement techniques. In this study, we address these challenges by introducing an open-source dataset (ADNP-15) of neuritic plaques (i.e., amyloid deposits combined with a crown of dystrophic tau-positive neurites) in human brain whole slide images. We establish a comprehensive benchmark by evaluating five widely adopted deep learning models across four stain normalization techniques, providing deeper insights into their influence on neuritic plaque segmentation. Additionally, we propose a novel image enhancement method that improves segmentation accuracy, particularly in complex tissue structures, by enhancing structural details and mitigating staining inconsistencies. Our experimental results demonstrate that this enhancement strategy significantly boosts model generalization and segmentation accuracy. All datasets and code are open-source, ensuring transparency and reproducibility while enabling further advancements in the field.

Graph Theory and GNNs to Unravel the Topographical Organization of Brain Lesions in Variants of Alzheimer's Disease Progression

This study utilizes graph theory and deep learning to assess variations in Alzheimer's disease (AD) neuropathologies, focusing on classic (cAD) and rapid (rpAD) progression forms. It analyses the distribution of amyloid plaques and tau tangles in postmortem brain tissues. Histopathological images are converted into tau-pathology-based graphs, and derived metrics are used for statistical analysis and in machine learning classifiers. These classifiers incorporate SHAP value explainability to differentiate between cAD and rpAD. Graph neural networks (GNNs) demonstrate greater efficiency than traditional CNN methods in analyzing this data, preserving spatial pathology context. Additionally, GNNs provide significant insights through explainable AI techniques. The analysis shows denser networks in rpAD and a distinctive impact on brain cortical layers: rpAD predominantly affects middle layers, whereas cAD influences both superficial and deep layers of the same cortical regions. These results suggest a unique neuropathological network organization for each AD variant.