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Identification of a Four-Gene Signature for Diagnosing Paediatric Sepsis

AIM: Early diagnosis of paediatric sepsis is crucial for the proper treatment of children and reduction of hospitalization and mortality. Biomarkers are a convenient and effective method for diagnosing any disease. However, huge differences among the studies reporting biomarkers for diagnosing sepsi...

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Autores principales: Yao, Yinhui, Zhao, Jingyi, Hu, Junhui, Song, Hong, Wang, Sizhu, Wang, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860560/
https://www.ncbi.nlm.nih.gov/pubmed/35198634
http://dx.doi.org/10.1155/2022/5217885
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author Yao, Yinhui
Zhao, Jingyi
Hu, Junhui
Song, Hong
Wang, Sizhu
Wang, Ying
author_facet Yao, Yinhui
Zhao, Jingyi
Hu, Junhui
Song, Hong
Wang, Sizhu
Wang, Ying
author_sort Yao, Yinhui
collection PubMed
description AIM: Early diagnosis of paediatric sepsis is crucial for the proper treatment of children and reduction of hospitalization and mortality. Biomarkers are a convenient and effective method for diagnosing any disease. However, huge differences among the studies reporting biomarkers for diagnosing sepsis have limited their clinical application. Therefore, in this study, we aimed to evaluate the diagnostic value of key genes involved in paediatric sepsis based on the data of the Gene Expression Omnibus database. METHODS: We used the GSE119217 dataset to identify differentially expressed genes (DEGs) between patients with and without paediatric sepsis. The most relevant gene modules of paediatric sepsis were screened through the weighted gene coexpression network analysis (WGCNA). Common genes (CGs) were found between DEGs and WGCNA. Genes with a potential diagnostic value in paediatric sepsis were selected from the CGs using least absolute shrinkage and selection operator regression and support vector machine recursive feature elimination. The principal component analysis, receiver operating characteristic curves, and C-index were used to verify the diagnostic value of the identified genes in six other independent sepsis datasets. Subsequently, a meta-analysis of the selected genes was performed to evaluate the value of these genes as biomarkers in paediatric sepsis. RESULTS: A total of 41 CGs were selected from the GSE119217 dataset. A four-gene signature composed of ANXA3, CD177, GRAMD1C, and TIGD3 effectively distinguished patients with paediatric sepsis from those in the control group. The signature was verified using six other independent datasets. In addition, the meta-analysis results showed that the pooled sensitivity, specificity, and area under the curve values were 1.00, 0.98, and 1.00, respectively. CONCLUSION: The four-gene signature can be used as new biomarkers to distinguish patients with paediatric sepsis from healthy individuals.
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spelling pubmed-88605602022-02-22 Identification of a Four-Gene Signature for Diagnosing Paediatric Sepsis Yao, Yinhui Zhao, Jingyi Hu, Junhui Song, Hong Wang, Sizhu Wang, Ying Biomed Res Int Research Article AIM: Early diagnosis of paediatric sepsis is crucial for the proper treatment of children and reduction of hospitalization and mortality. Biomarkers are a convenient and effective method for diagnosing any disease. However, huge differences among the studies reporting biomarkers for diagnosing sepsis have limited their clinical application. Therefore, in this study, we aimed to evaluate the diagnostic value of key genes involved in paediatric sepsis based on the data of the Gene Expression Omnibus database. METHODS: We used the GSE119217 dataset to identify differentially expressed genes (DEGs) between patients with and without paediatric sepsis. The most relevant gene modules of paediatric sepsis were screened through the weighted gene coexpression network analysis (WGCNA). Common genes (CGs) were found between DEGs and WGCNA. Genes with a potential diagnostic value in paediatric sepsis were selected from the CGs using least absolute shrinkage and selection operator regression and support vector machine recursive feature elimination. The principal component analysis, receiver operating characteristic curves, and C-index were used to verify the diagnostic value of the identified genes in six other independent sepsis datasets. Subsequently, a meta-analysis of the selected genes was performed to evaluate the value of these genes as biomarkers in paediatric sepsis. RESULTS: A total of 41 CGs were selected from the GSE119217 dataset. A four-gene signature composed of ANXA3, CD177, GRAMD1C, and TIGD3 effectively distinguished patients with paediatric sepsis from those in the control group. The signature was verified using six other independent datasets. In addition, the meta-analysis results showed that the pooled sensitivity, specificity, and area under the curve values were 1.00, 0.98, and 1.00, respectively. CONCLUSION: The four-gene signature can be used as new biomarkers to distinguish patients with paediatric sepsis from healthy individuals. Hindawi 2022-02-14 /pmc/articles/PMC8860560/ /pubmed/35198634 http://dx.doi.org/10.1155/2022/5217885 Text en Copyright © 2022 Yinhui Yao et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yao, Yinhui
Zhao, Jingyi
Hu, Junhui
Song, Hong
Wang, Sizhu
Wang, Ying
Identification of a Four-Gene Signature for Diagnosing Paediatric Sepsis
title Identification of a Four-Gene Signature for Diagnosing Paediatric Sepsis
title_full Identification of a Four-Gene Signature for Diagnosing Paediatric Sepsis
title_fullStr Identification of a Four-Gene Signature for Diagnosing Paediatric Sepsis
title_full_unstemmed Identification of a Four-Gene Signature for Diagnosing Paediatric Sepsis
title_short Identification of a Four-Gene Signature for Diagnosing Paediatric Sepsis
title_sort identification of a four-gene signature for diagnosing paediatric sepsis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860560/
https://www.ncbi.nlm.nih.gov/pubmed/35198634
http://dx.doi.org/10.1155/2022/5217885
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