A Diagnostic Model for Alzheimer’s Disease Based on Blood Levels of Autophagy-Related Genes

Alzheimer’s disease (AD) is a common neurodegenerative disease. The major problems that exist in the diagnosis of AD include the costly examinations and the high-invasive sampling tissue. Therefore, it would be advantageous to develop blood biomarkers. Because AD’s pathological process is considered...

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Main Authors: Qiangqiang Qin, Zhanfeng Gu, Fei Li, Yanbing Pan, TianXiang Zhang, Yang Fang, Lesha Zhang
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-05-01
Series:Frontiers in Aging Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnagi.2022.881890/full
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author Qiangqiang Qin
Zhanfeng Gu
Fei Li
Yanbing Pan
TianXiang Zhang
Yang Fang
Lesha Zhang
author_facet Qiangqiang Qin
Zhanfeng Gu
Fei Li
Yanbing Pan
TianXiang Zhang
Yang Fang
Lesha Zhang
author_sort Qiangqiang Qin
collection DOAJ
description Alzheimer’s disease (AD) is a common neurodegenerative disease. The major problems that exist in the diagnosis of AD include the costly examinations and the high-invasive sampling tissue. Therefore, it would be advantageous to develop blood biomarkers. Because AD’s pathological process is considered tightly related to autophagy; thus, a diagnostic model for AD based on ATGs may have more predictive accuracy than other models. We obtained GSE63060 dataset from the GEO database, ATGs from the HADb and screened 64 differentially expressed autophagy-related genes (DE-ATGs). We then applied them to Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses as well as DisGeNET and PaGenBase enrichment analyses. By using the univariate analysis, least absolute shrinkage and selection operator (LASSO) regression method and the multivariable logistic regression, nine DE-ATGs were identified as biomarkers, which are ATG16L2, BAK1, CAPN10, CASP1, RAB24, RGS19, RPS6KB1, ULK2, and WDFY3. We combined them with sex and age to establish a nomogram model. To evaluate the model’s distinguishability, consistency, and clinical applicability, we applied the receiver operating characteristic (ROC) curve, C-index, calibration curve, and on the validation datasets GSE63061, GSE54536, GSE22255, and GSE151371 from GEO database. The results show that our model demonstrates good prediction performance. This AD diagnosis model may benefit both clinical work and mechanistic research.
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spelling doaj.art-7b1f0d9e72ab4dc9ab18ba0c026f41fc2022-12-22T00:38:35ZengFrontiers Media S.A.Frontiers in Aging Neuroscience1663-43652022-05-011410.3389/fnagi.2022.881890881890A Diagnostic Model for Alzheimer’s Disease Based on Blood Levels of Autophagy-Related GenesQiangqiang Qin0Zhanfeng Gu1Fei Li2Yanbing Pan3TianXiang Zhang4Yang Fang5Lesha Zhang6Second Institute of Clinical Medicine, Anhui Medical University, Hefei, ChinaSecond Institute of Clinical Medicine, Anhui Medical University, Hefei, ChinaSecond Institute of Clinical Medicine, Anhui Medical University, Hefei, ChinaSecond Institute of Clinical Medicine, Anhui Medical University, Hefei, ChinaSecond Institute of Clinical Medicine, Anhui Medical University, Hefei, ChinaDepartment of Physiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, ChinaDepartment of Physiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, ChinaAlzheimer’s disease (AD) is a common neurodegenerative disease. The major problems that exist in the diagnosis of AD include the costly examinations and the high-invasive sampling tissue. Therefore, it would be advantageous to develop blood biomarkers. Because AD’s pathological process is considered tightly related to autophagy; thus, a diagnostic model for AD based on ATGs may have more predictive accuracy than other models. We obtained GSE63060 dataset from the GEO database, ATGs from the HADb and screened 64 differentially expressed autophagy-related genes (DE-ATGs). We then applied them to Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses as well as DisGeNET and PaGenBase enrichment analyses. By using the univariate analysis, least absolute shrinkage and selection operator (LASSO) regression method and the multivariable logistic regression, nine DE-ATGs were identified as biomarkers, which are ATG16L2, BAK1, CAPN10, CASP1, RAB24, RGS19, RPS6KB1, ULK2, and WDFY3. We combined them with sex and age to establish a nomogram model. To evaluate the model’s distinguishability, consistency, and clinical applicability, we applied the receiver operating characteristic (ROC) curve, C-index, calibration curve, and on the validation datasets GSE63061, GSE54536, GSE22255, and GSE151371 from GEO database. The results show that our model demonstrates good prediction performance. This AD diagnosis model may benefit both clinical work and mechanistic research.https://www.frontiersin.org/articles/10.3389/fnagi.2022.881890/fullAlzheimer’s disease (AD)autophagyDEGsnomogramLASSO
spellingShingle Qiangqiang Qin
Zhanfeng Gu
Fei Li
Yanbing Pan
TianXiang Zhang
Yang Fang
Lesha Zhang
A Diagnostic Model for Alzheimer’s Disease Based on Blood Levels of Autophagy-Related Genes
Frontiers in Aging Neuroscience
Alzheimer’s disease (AD)
autophagy
DEGs
nomogram
LASSO
title A Diagnostic Model for Alzheimer’s Disease Based on Blood Levels of Autophagy-Related Genes
title_full A Diagnostic Model for Alzheimer’s Disease Based on Blood Levels of Autophagy-Related Genes
title_fullStr A Diagnostic Model for Alzheimer’s Disease Based on Blood Levels of Autophagy-Related Genes
title_full_unstemmed A Diagnostic Model for Alzheimer’s Disease Based on Blood Levels of Autophagy-Related Genes
title_short A Diagnostic Model for Alzheimer’s Disease Based on Blood Levels of Autophagy-Related Genes
title_sort diagnostic model for alzheimer s disease based on blood levels of autophagy related genes
topic Alzheimer’s disease (AD)
autophagy
DEGs
nomogram
LASSO
url https://www.frontiersin.org/articles/10.3389/fnagi.2022.881890/full
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