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Identification of key immune genes of osteoporosis based on bioinformatics and machine learning

INTRODUCTION: Immunity is involved in a variety of bone metabolic processes, especially osteoporosis. The aim of this study is to explore new bone immune-related markers by bioinformatics method and evaluate their ability to predict osteoporosis. METHODS: The mRNA expression profiles were obtained f...

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Autores principales: Hao, Song, Xinqi, Mao, Weicheng, Xu, Shiwei, Yang, Lumin, Cao, Xiao, Wang, Dong, Liu, Jun, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10289263/
https://www.ncbi.nlm.nih.gov/pubmed/37361541
http://dx.doi.org/10.3389/fendo.2023.1118886
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author Hao, Song
Xinqi, Mao
Weicheng, Xu
Shiwei, Yang
Lumin, Cao
Xiao, Wang
Dong, Liu
Jun, Hua
author_facet Hao, Song
Xinqi, Mao
Weicheng, Xu
Shiwei, Yang
Lumin, Cao
Xiao, Wang
Dong, Liu
Jun, Hua
author_sort Hao, Song
collection PubMed
description INTRODUCTION: Immunity is involved in a variety of bone metabolic processes, especially osteoporosis. The aim of this study is to explore new bone immune-related markers by bioinformatics method and evaluate their ability to predict osteoporosis. METHODS: The mRNA expression profiles were obtained from GSE7158 in Gene expression Omnibus (GEO), and immune-related genes were obtained from ImmPort database (https://www.immport.org/shared/). immune genes related to bone mineral density(BMD) were screened out for differential analysis. protein-protein interaction (PPIs) networks were used to analyze the interrelationships between different immune-related genes (DIRGs). Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses of DIRGs function were performed. A least absolute shrinkage and selection operation (LASSO) regression model and multiple Support Vector Machine-Recursive Feature Elimination (mSVM-RFE) model were constructed to identify the candidate genes for osteoporosis prediction The receiver operator characteristic (ROC) curves were used to validate the performances of predictive models and candidate genes in GEO database (GSE7158,GSE13850).Through the RT - qPCR verify the key genes differentially expressed in peripheral blood mononuclear cells Finally, we constructed a nomogram model for predicting osteoporosis based on five immune-related genes. CIBERSORT algorithm was used to calculate the relative proportion of 22 immune cells. RESULTS: A total of 1158 DEGs and 66 DIRGs were identified between high-BMD and low-BMD women. These DIRGs were mainly enriched in cytokine−mediated signaling pathway, positive regulation of response to external stimulus and the cellular components of genes are mostly localized to external side of plasma membrane. And the KEGG enrichment analysis were mainly involved in Cytokine−cytokine receptor interaction, PI3K−Akt signaling pathway, Neuroactive ligand−receptor interaction,Natural killer cell mediated cytotoxicity. Then five key genes (CCR5, IAPP, IFNA4, IGHV3-73 and PTGER1) were identified and used as features to construct a predictive prognostic model for osteoporosis using the GSE7158 dataset. CONCLUSION: Immunity plays an important role in the development of osteoporosis.CCR5, IAPP, IFNA4, IGHV3-73 and PTGER1were play an important role in the occurrences and diagnosis of OP.
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spelling pubmed-102892632023-06-24 Identification of key immune genes of osteoporosis based on bioinformatics and machine learning Hao, Song Xinqi, Mao Weicheng, Xu Shiwei, Yang Lumin, Cao Xiao, Wang Dong, Liu Jun, Hua Front Endocrinol (Lausanne) Endocrinology INTRODUCTION: Immunity is involved in a variety of bone metabolic processes, especially osteoporosis. The aim of this study is to explore new bone immune-related markers by bioinformatics method and evaluate their ability to predict osteoporosis. METHODS: The mRNA expression profiles were obtained from GSE7158 in Gene expression Omnibus (GEO), and immune-related genes were obtained from ImmPort database (https://www.immport.org/shared/). immune genes related to bone mineral density(BMD) were screened out for differential analysis. protein-protein interaction (PPIs) networks were used to analyze the interrelationships between different immune-related genes (DIRGs). Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses of DIRGs function were performed. A least absolute shrinkage and selection operation (LASSO) regression model and multiple Support Vector Machine-Recursive Feature Elimination (mSVM-RFE) model were constructed to identify the candidate genes for osteoporosis prediction The receiver operator characteristic (ROC) curves were used to validate the performances of predictive models and candidate genes in GEO database (GSE7158,GSE13850).Through the RT - qPCR verify the key genes differentially expressed in peripheral blood mononuclear cells Finally, we constructed a nomogram model for predicting osteoporosis based on five immune-related genes. CIBERSORT algorithm was used to calculate the relative proportion of 22 immune cells. RESULTS: A total of 1158 DEGs and 66 DIRGs were identified between high-BMD and low-BMD women. These DIRGs were mainly enriched in cytokine−mediated signaling pathway, positive regulation of response to external stimulus and the cellular components of genes are mostly localized to external side of plasma membrane. And the KEGG enrichment analysis were mainly involved in Cytokine−cytokine receptor interaction, PI3K−Akt signaling pathway, Neuroactive ligand−receptor interaction,Natural killer cell mediated cytotoxicity. Then five key genes (CCR5, IAPP, IFNA4, IGHV3-73 and PTGER1) were identified and used as features to construct a predictive prognostic model for osteoporosis using the GSE7158 dataset. CONCLUSION: Immunity plays an important role in the development of osteoporosis.CCR5, IAPP, IFNA4, IGHV3-73 and PTGER1were play an important role in the occurrences and diagnosis of OP. Frontiers Media S.A. 2023-06-07 /pmc/articles/PMC10289263/ /pubmed/37361541 http://dx.doi.org/10.3389/fendo.2023.1118886 Text en Copyright © 2023 Hao, Xinqi, Weicheng, Shiwei, Lumin, Xiao, Dong and Jun 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 Endocrinology
Hao, Song
Xinqi, Mao
Weicheng, Xu
Shiwei, Yang
Lumin, Cao
Xiao, Wang
Dong, Liu
Jun, Hua
Identification of key immune genes of osteoporosis based on bioinformatics and machine learning
title Identification of key immune genes of osteoporosis based on bioinformatics and machine learning
title_full Identification of key immune genes of osteoporosis based on bioinformatics and machine learning
title_fullStr Identification of key immune genes of osteoporosis based on bioinformatics and machine learning
title_full_unstemmed Identification of key immune genes of osteoporosis based on bioinformatics and machine learning
title_short Identification of key immune genes of osteoporosis based on bioinformatics and machine learning
title_sort identification of key immune genes of osteoporosis based on bioinformatics and machine learning
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10289263/
https://www.ncbi.nlm.nih.gov/pubmed/37361541
http://dx.doi.org/10.3389/fendo.2023.1118886
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