» Articles » PMID: 36547067

Interpretable Classification of Tauopathies with a Convolutional Neural Network Pipeline Using Transfer Learning and Validation Against Post-Mortem Clinical Cases of Alzheimer's Disease and Progressive Supranuclear Palsy

Overview
Publisher MDPI
Specialty Molecular Biology
Date 2022 Dec 22
PMID 36547067
Authors
Affiliations
Soon will be listed here.
Abstract

Neurodegenerative diseases, tauopathies, constitute a serious global health problem. The etiology of these diseases is unclear and an increase in their incidence has been projected in the next 30 years. Therefore, the study of the molecular mechanisms that might stop these neurodegenerative processes is very relevant. Classification of neurodegenerative diseases using Machine and Deep Learning algorithms has been widely studied for medical imaging such as Magnetic Resonance Imaging. However, post-mortem immunofluorescence imaging studies of the brains of patients have not yet been used for this purpose. These studies may represent a valuable tool for monitoring aberrant chemical changes or pathological post-translational modifications of the Tau polypeptide. We propose a Convolutional Neural Network pipeline for the classification of Tau pathology of Alzheimer's disease and Progressive Supranuclear Palsy by analyzing post-mortem immunofluorescence images with different Tau biomarkers performed with models generated with the architecture ResNet-IFT using Transfer Learning. These models' outputs were interpreted with interpretability algorithms such as Guided Grad-CAM and Occlusion Analysis. To determine the best classifier, four different architectures were tested. We demonstrated that our design was able to classify diseases with an accuracy of 98.41% on average whilst providing an interpretation concerning the proper classification involving different structural patterns in the immunoreactivity of the Tau protein in NFTs present in the brains of patients with Progressive Supranuclear Palsy and Alzheimer's disease.

Citing Articles

Explainable Machine Learning Models for Brain Diseases: Insights from a Systematic Review.

Rodriguez Mallma M, Zuloaga-Rotta L, Borja-Rosales R, Rodriguez Mallma J, Vilca-Aguilar M, Salas-Ojeda M Neurol Int. 2024; 16(6):1285-1307.

PMID: 39585057 PMC: 11587041. DOI: 10.3390/neurolint16060098.


Enhancing IoT Network Security: Unveiling the Power of Self-Supervised Learning against DDoS Attacks.

Almaraz-Rivera J, Cantoral-Ceballos J, Botero J Sensors (Basel). 2023; 23(21).

PMID: 37960401 PMC: 10647748. DOI: 10.3390/s23218701.


Deep Learning Aided Neuroimaging and Brain Regulation.

Xu M, Ouyang Y, Yuan Z Sensors (Basel). 2023; 23(11).

PMID: 37299724 PMC: 10255716. DOI: 10.3390/s23114993.

References
1.
Alegro M, Theofilas P, Nguy A, Castruita P, Seeley W, Heinsen H . Automating cell detection and classification in human brain fluorescent microscopy images using dictionary learning and sparse coding. J Neurosci Methods. 2017; 282:20-33. PMC: 5600818. DOI: 10.1016/j.jneumeth.2017.03.002. View

2.
Dugger B, Dickson D . Pathology of Neurodegenerative Diseases. Cold Spring Harb Perspect Biol. 2017; 9(7). PMC: 5495060. DOI: 10.1101/cshperspect.a028035. View

3.
Savastano A, Flores D, Kadavath H, Biernat J, Mandelkow E, Zweckstetter M . Disease-Associated Tau Phosphorylation Hinders Tubulin Assembly within Tau Condensates. Angew Chem Int Ed Engl. 2020; 60(2):726-730. PMC: 7839466. DOI: 10.1002/anie.202011157. View

4.
Gao X, Hui R, Tian Z . Classification of CT brain images based on deep learning networks. Comput Methods Programs Biomed. 2016; 138:49-56. DOI: 10.1016/j.cmpb.2016.10.007. View

5.
Shakir M, Dugger B . Advances in Deep Neuropathological Phenotyping of Alzheimer Disease: Past, Present, and Future. J Neuropathol Exp Neurol. 2022; 81(1):2-15. PMC: 8825756. DOI: 10.1093/jnen/nlab122. View