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Development and validation of immune-based biomarkers and deep learning models for Alzheimer’s disease

Background: Alzheimer’s disease (AD) is the most common form of dementia in old age and poses a severe threat to the health and life of the elderly. However, traditional diagnostic methods and the ATN diagnostic framework have limitations in clinical practice. Developing novel biomarkers and diagnos...

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Autores principales: He, Yijie, Cong, Lin, He, Qinfei, Feng, Nianping, Wu, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441688/
https://www.ncbi.nlm.nih.gov/pubmed/36072674
http://dx.doi.org/10.3389/fgene.2022.968598
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author He, Yijie
Cong, Lin
He, Qinfei
Feng, Nianping
Wu, Yun
author_facet He, Yijie
Cong, Lin
He, Qinfei
Feng, Nianping
Wu, Yun
author_sort He, Yijie
collection PubMed
description Background: Alzheimer’s disease (AD) is the most common form of dementia in old age and poses a severe threat to the health and life of the elderly. However, traditional diagnostic methods and the ATN diagnostic framework have limitations in clinical practice. Developing novel biomarkers and diagnostic models is necessary to complement existing diagnostic procedures. Methods: The AD expression profile dataset GSE63060 was downloaded from the NCBI GEO public database for preprocessing. AD-related differentially expressed genes were screened using a weighted co-expression network and differential expression analysis, and functional enrichment analysis was performed. Subsequently, we screened hub genes by random forest, analyzed the correlation between hub genes and immune cells using ssGSEA, and finally built an AD diagnostic model using an artificial neural network and validated it. Results: Based on the random forest algorithm, we screened a total of seven hub genes from AD-related DEGs, based on which we confirmed that hub genes play an essential role in the immune microenvironment and successfully established a novel diagnostic model for AD using artificial neural networks, and validated its effectiveness in the publicly available datasets GSE63060 and GSE97760. Conclusion: Our study establishes a reliable model for screening and diagnosing AD that provides a theoretical basis for adding diagnostic biomarkers for the AD gene.
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spelling pubmed-94416882022-09-06 Development and validation of immune-based biomarkers and deep learning models for Alzheimer’s disease He, Yijie Cong, Lin He, Qinfei Feng, Nianping Wu, Yun Front Genet Genetics Background: Alzheimer’s disease (AD) is the most common form of dementia in old age and poses a severe threat to the health and life of the elderly. However, traditional diagnostic methods and the ATN diagnostic framework have limitations in clinical practice. Developing novel biomarkers and diagnostic models is necessary to complement existing diagnostic procedures. Methods: The AD expression profile dataset GSE63060 was downloaded from the NCBI GEO public database for preprocessing. AD-related differentially expressed genes were screened using a weighted co-expression network and differential expression analysis, and functional enrichment analysis was performed. Subsequently, we screened hub genes by random forest, analyzed the correlation between hub genes and immune cells using ssGSEA, and finally built an AD diagnostic model using an artificial neural network and validated it. Results: Based on the random forest algorithm, we screened a total of seven hub genes from AD-related DEGs, based on which we confirmed that hub genes play an essential role in the immune microenvironment and successfully established a novel diagnostic model for AD using artificial neural networks, and validated its effectiveness in the publicly available datasets GSE63060 and GSE97760. Conclusion: Our study establishes a reliable model for screening and diagnosing AD that provides a theoretical basis for adding diagnostic biomarkers for the AD gene. Frontiers Media S.A. 2022-08-22 /pmc/articles/PMC9441688/ /pubmed/36072674 http://dx.doi.org/10.3389/fgene.2022.968598 Text en Copyright © 2022 He, Cong, He, Feng and Wu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
He, Yijie
Cong, Lin
He, Qinfei
Feng, Nianping
Wu, Yun
Development and validation of immune-based biomarkers and deep learning models for Alzheimer’s disease
title Development and validation of immune-based biomarkers and deep learning models for Alzheimer’s disease
title_full Development and validation of immune-based biomarkers and deep learning models for Alzheimer’s disease
title_fullStr Development and validation of immune-based biomarkers and deep learning models for Alzheimer’s disease
title_full_unstemmed Development and validation of immune-based biomarkers and deep learning models for Alzheimer’s disease
title_short Development and validation of immune-based biomarkers and deep learning models for Alzheimer’s disease
title_sort development and validation of immune-based biomarkers and deep learning models for alzheimer’s disease
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441688/
https://www.ncbi.nlm.nih.gov/pubmed/36072674
http://dx.doi.org/10.3389/fgene.2022.968598
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