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Quantitative analysis of prion disease using an AI-powered digital pathology framework

Prion disease is a fatal neurodegenerative disorder characterized by accumulation of an abnormal prion protein (PrPSc) in the central nervous system. To identify PrPSc aggregates for diagnostic purposes, pathologists use immunohistochemical staining of prion protein antibodies on tissue samples. Wit...

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Autores principales: Salvi, Massimo, Molinari, Filippo, Ciccarelli, Mario, Testi, Roberto, Taraglio, Stefano, Imperiale, Daniele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584956/
https://www.ncbi.nlm.nih.gov/pubmed/37853094
http://dx.doi.org/10.1038/s41598-023-44782-4
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author Salvi, Massimo
Molinari, Filippo
Ciccarelli, Mario
Testi, Roberto
Taraglio, Stefano
Imperiale, Daniele
author_facet Salvi, Massimo
Molinari, Filippo
Ciccarelli, Mario
Testi, Roberto
Taraglio, Stefano
Imperiale, Daniele
author_sort Salvi, Massimo
collection PubMed
description Prion disease is a fatal neurodegenerative disorder characterized by accumulation of an abnormal prion protein (PrPSc) in the central nervous system. To identify PrPSc aggregates for diagnostic purposes, pathologists use immunohistochemical staining of prion protein antibodies on tissue samples. With digital pathology, artificial intelligence can now analyze stained slides. In this study, we developed an automated pipeline for the identification of PrPSc aggregates in tissue samples from the cerebellar and occipital cortex. To the best of our knowledge, this is the first framework to evaluate PrPSc deposition in digital images. We used two strategies: a deep learning segmentation approach using a vision transformer, and a machine learning classification approach with traditional classifiers. Our method was developed and tested on 64 whole slide images from 41 patients definitively diagnosed with prion disease. The results of our study demonstrated that our proposed framework can accurately classify WSIs from a blind test set. Moreover, it can quantify PrPSc distribution and localization throughout the brain. This could potentially be extended to evaluate protein expression in other neurodegenerative diseases like Alzheimer's and Parkinson's. Overall, our pipeline highlights the potential of AI-assisted pathology to provide valuable insights, leading to improved diagnostic accuracy and efficiency.
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spelling pubmed-105849562023-10-20 Quantitative analysis of prion disease using an AI-powered digital pathology framework Salvi, Massimo Molinari, Filippo Ciccarelli, Mario Testi, Roberto Taraglio, Stefano Imperiale, Daniele Sci Rep Article Prion disease is a fatal neurodegenerative disorder characterized by accumulation of an abnormal prion protein (PrPSc) in the central nervous system. To identify PrPSc aggregates for diagnostic purposes, pathologists use immunohistochemical staining of prion protein antibodies on tissue samples. With digital pathology, artificial intelligence can now analyze stained slides. In this study, we developed an automated pipeline for the identification of PrPSc aggregates in tissue samples from the cerebellar and occipital cortex. To the best of our knowledge, this is the first framework to evaluate PrPSc deposition in digital images. We used two strategies: a deep learning segmentation approach using a vision transformer, and a machine learning classification approach with traditional classifiers. Our method was developed and tested on 64 whole slide images from 41 patients definitively diagnosed with prion disease. The results of our study demonstrated that our proposed framework can accurately classify WSIs from a blind test set. Moreover, it can quantify PrPSc distribution and localization throughout the brain. This could potentially be extended to evaluate protein expression in other neurodegenerative diseases like Alzheimer's and Parkinson's. Overall, our pipeline highlights the potential of AI-assisted pathology to provide valuable insights, leading to improved diagnostic accuracy and efficiency. Nature Publishing Group UK 2023-10-18 /pmc/articles/PMC10584956/ /pubmed/37853094 http://dx.doi.org/10.1038/s41598-023-44782-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Salvi, Massimo
Molinari, Filippo
Ciccarelli, Mario
Testi, Roberto
Taraglio, Stefano
Imperiale, Daniele
Quantitative analysis of prion disease using an AI-powered digital pathology framework
title Quantitative analysis of prion disease using an AI-powered digital pathology framework
title_full Quantitative analysis of prion disease using an AI-powered digital pathology framework
title_fullStr Quantitative analysis of prion disease using an AI-powered digital pathology framework
title_full_unstemmed Quantitative analysis of prion disease using an AI-powered digital pathology framework
title_short Quantitative analysis of prion disease using an AI-powered digital pathology framework
title_sort quantitative analysis of prion disease using an ai-powered digital pathology framework
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584956/
https://www.ncbi.nlm.nih.gov/pubmed/37853094
http://dx.doi.org/10.1038/s41598-023-44782-4
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