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Identification of macrophage-related genes in sepsis-induced ARDS using bioinformatics and machine learning
Sepsis-induced acute respiratory distress syndrome (ARDS) is one of the leading causes of death in critically ill patients, and macrophages play very important roles in the pathogenesis and treatment of sepsis-induced ARDS. The aim of this study was to screen macrophage-related biomarkers for the di...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10279743/ https://www.ncbi.nlm.nih.gov/pubmed/37336980 http://dx.doi.org/10.1038/s41598-023-37162-5 |
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author | Li, Qiuyue Zheng, Hongyu Chen, Bing |
author_facet | Li, Qiuyue Zheng, Hongyu Chen, Bing |
author_sort | Li, Qiuyue |
collection | PubMed |
description | Sepsis-induced acute respiratory distress syndrome (ARDS) is one of the leading causes of death in critically ill patients, and macrophages play very important roles in the pathogenesis and treatment of sepsis-induced ARDS. The aim of this study was to screen macrophage-related biomarkers for the diagnosis and treatment of sepsis-induced ARDS by bioinformatics and machine learning algorithms. A dataset including gene expression profiles of sepsis-induced ARDS patients and healthy controls was downloaded from the gene expression omnibus database. The limma package was used to screen 325 differentially expressed genes, and enrichment analysis suggested enrichment mainly in immune-related pathways and reactive oxygen metabolism pathways. The level of immune cell infiltration was analysed using the ssGSEA method, and then 506 macrophage-related genes were screened using WGCNA; 48 showed differential expression. PPI analysis was also performed. SVM-RFE and random forest map analysis were used to screen 10 genes. Three key genes, SGK1, DYSF and MSRB1, were obtained after validation with external datasets. ROC curves suggested that all three genes had good diagnostic efficacy. The nomogram model consisting of the three genes also had good diagnostic efficacy. This study provides new targets for the early diagnosis of sepsis-induced ARDS. |
format | Online Article Text |
id | pubmed-10279743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102797432023-06-21 Identification of macrophage-related genes in sepsis-induced ARDS using bioinformatics and machine learning Li, Qiuyue Zheng, Hongyu Chen, Bing Sci Rep Article Sepsis-induced acute respiratory distress syndrome (ARDS) is one of the leading causes of death in critically ill patients, and macrophages play very important roles in the pathogenesis and treatment of sepsis-induced ARDS. The aim of this study was to screen macrophage-related biomarkers for the diagnosis and treatment of sepsis-induced ARDS by bioinformatics and machine learning algorithms. A dataset including gene expression profiles of sepsis-induced ARDS patients and healthy controls was downloaded from the gene expression omnibus database. The limma package was used to screen 325 differentially expressed genes, and enrichment analysis suggested enrichment mainly in immune-related pathways and reactive oxygen metabolism pathways. The level of immune cell infiltration was analysed using the ssGSEA method, and then 506 macrophage-related genes were screened using WGCNA; 48 showed differential expression. PPI analysis was also performed. SVM-RFE and random forest map analysis were used to screen 10 genes. Three key genes, SGK1, DYSF and MSRB1, were obtained after validation with external datasets. ROC curves suggested that all three genes had good diagnostic efficacy. The nomogram model consisting of the three genes also had good diagnostic efficacy. This study provides new targets for the early diagnosis of sepsis-induced ARDS. Nature Publishing Group UK 2023-06-19 /pmc/articles/PMC10279743/ /pubmed/37336980 http://dx.doi.org/10.1038/s41598-023-37162-5 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 Li, Qiuyue Zheng, Hongyu Chen, Bing Identification of macrophage-related genes in sepsis-induced ARDS using bioinformatics and machine learning |
title | Identification of macrophage-related genes in sepsis-induced ARDS using bioinformatics and machine learning |
title_full | Identification of macrophage-related genes in sepsis-induced ARDS using bioinformatics and machine learning |
title_fullStr | Identification of macrophage-related genes in sepsis-induced ARDS using bioinformatics and machine learning |
title_full_unstemmed | Identification of macrophage-related genes in sepsis-induced ARDS using bioinformatics and machine learning |
title_short | Identification of macrophage-related genes in sepsis-induced ARDS using bioinformatics and machine learning |
title_sort | identification of macrophage-related genes in sepsis-induced ards using bioinformatics and machine learning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10279743/ https://www.ncbi.nlm.nih.gov/pubmed/37336980 http://dx.doi.org/10.1038/s41598-023-37162-5 |
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