Visual Deep Learning-Based Explanation for Neuritic Plaques Segmentation in Alzheimer's Disease Using Weakly Annotated Whole Slide Histopathological Images

Quantifying the distribution and morphology of tau protein structures in brain tissues is key to diagnosing Alzheimer's Disease (AD) and its subtypes. Recently, deep learning (DL) models such as UNet have been successfully used for automatic segmentation of histopathological whole slide images (WSI) of biological tissues. In this study, we propose a DL-based methodology for semantic segmentation of tau lesions (i.e., neuritic plaques) in WSI of postmortem patients with AD. The state of the art in semantic segmentation of neuritic plaques in human WSI is very limited. Our study proposes a baseline able to generate a significant advantage for morphological analysis of these tauopathies for further stratification of AD patients. Essential discussions concerning biomarkers (ALZ50 versus AT8 tau antibodies), the imaging modality (different slide scanner resolutions), and the challenge of weak annotations are addressed within this seminal study. The analysis of the impact of context in plaque segmentation is important to understand the role of the micro-environment for reliable tau protein segmentation. In addition, by integrating visual interpretability, we are able to explain how the network focuses on a region of interest (ROI), giving additional insights to pathologists. Finally, the release of a new expert-annotated database and the code (https://github.com/aramis-lab/miccai2022-stratifiad.git) will be helpful for the scientific community to accelerate the development of new pipelines for human WSI processing in AD.

Automated summary

This study introduces a DL-based method for semantic segmentation of tau lesions in brain tissues of AD patients, providing significant advantages for further stratification. Discussions on biomarkers, imaging modalities, and weak annotation challenges are crucial in this seminal research.