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Identification of biomarkers associated with pediatric asthma using machine learning algorithms: A review

Pediatric asthma is a complex disease with a multifactorial etiology. The identification of biomarkers associated with pediatric asthma can provide insights into the pathogenesis of the disease and aid in the development of novel diagnostic and therapeutic strategies. This study aimed to identify po...

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Autores principales: Lin, Kexin, Wang, Yijie, Li, Yongjun, Wang, Youpeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10681392/
https://www.ncbi.nlm.nih.gov/pubmed/38013370
http://dx.doi.org/10.1097/MD.0000000000036070
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author Lin, Kexin
Wang, Yijie
Li, Yongjun
Wang, Youpeng
author_facet Lin, Kexin
Wang, Yijie
Li, Yongjun
Wang, Youpeng
author_sort Lin, Kexin
collection PubMed
description Pediatric asthma is a complex disease with a multifactorial etiology. The identification of biomarkers associated with pediatric asthma can provide insights into the pathogenesis of the disease and aid in the development of novel diagnostic and therapeutic strategies. This study aimed to identify potential biomarkers for pediatric asthma using Weighted Gene Co-expression Network Analysis (WGCNA) and machine learning algorithms. We obtained gene expression data from publicly available databases and performed WGCNA to identify gene co-expression modules associated with pediatric asthma. We then used machine learning algorithms, including random forest, lasso regression algorithm, and support vector machine-recursive feature elimination, to classify asthma cases and controls based on the identified gene modules. We also performed functional enrichment analyses to investigate the biological functions of the identified genes.We detected 24,544 genes exhibiting differential expression between controlled and uncontrolled genes from the GSE135192 dataset. In the combined WCGNA analysis, a total of 104 co-expression genes were screened, both controlled and uncontrolled. After screening, 11 hub genes were identified. They were AK2, PDK4, PER3, GZMH, NUMBL, NRL, SCO2, CREBZF, LARP1B, RXFP1, and VDAC3P1. The areas under their receiver operating characteristic curve were above 0.78. Our study identified potential biomarkers for pediatric asthma using WGCNA and machine learning algorithms. Our findings suggest that 11 hub genes could be used as novel diagnostic markers and treatment targets for pediatric asthma. These findings provide new insights into the pathogenesis of pediatric asthma and may aid in the development of novel diagnostic and therapeutic strategies.
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spelling pubmed-106813922023-11-24 Identification of biomarkers associated with pediatric asthma using machine learning algorithms: A review Lin, Kexin Wang, Yijie Li, Yongjun Wang, Youpeng Medicine (Baltimore) 6200 Pediatric asthma is a complex disease with a multifactorial etiology. The identification of biomarkers associated with pediatric asthma can provide insights into the pathogenesis of the disease and aid in the development of novel diagnostic and therapeutic strategies. This study aimed to identify potential biomarkers for pediatric asthma using Weighted Gene Co-expression Network Analysis (WGCNA) and machine learning algorithms. We obtained gene expression data from publicly available databases and performed WGCNA to identify gene co-expression modules associated with pediatric asthma. We then used machine learning algorithms, including random forest, lasso regression algorithm, and support vector machine-recursive feature elimination, to classify asthma cases and controls based on the identified gene modules. We also performed functional enrichment analyses to investigate the biological functions of the identified genes.We detected 24,544 genes exhibiting differential expression between controlled and uncontrolled genes from the GSE135192 dataset. In the combined WCGNA analysis, a total of 104 co-expression genes were screened, both controlled and uncontrolled. After screening, 11 hub genes were identified. They were AK2, PDK4, PER3, GZMH, NUMBL, NRL, SCO2, CREBZF, LARP1B, RXFP1, and VDAC3P1. The areas under their receiver operating characteristic curve were above 0.78. Our study identified potential biomarkers for pediatric asthma using WGCNA and machine learning algorithms. Our findings suggest that 11 hub genes could be used as novel diagnostic markers and treatment targets for pediatric asthma. These findings provide new insights into the pathogenesis of pediatric asthma and may aid in the development of novel diagnostic and therapeutic strategies. Lippincott Williams & Wilkins 2023-11-24 /pmc/articles/PMC10681392/ /pubmed/38013370 http://dx.doi.org/10.1097/MD.0000000000036070 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle 6200
Lin, Kexin
Wang, Yijie
Li, Yongjun
Wang, Youpeng
Identification of biomarkers associated with pediatric asthma using machine learning algorithms: A review
title Identification of biomarkers associated with pediatric asthma using machine learning algorithms: A review
title_full Identification of biomarkers associated with pediatric asthma using machine learning algorithms: A review
title_fullStr Identification of biomarkers associated with pediatric asthma using machine learning algorithms: A review
title_full_unstemmed Identification of biomarkers associated with pediatric asthma using machine learning algorithms: A review
title_short Identification of biomarkers associated with pediatric asthma using machine learning algorithms: A review
title_sort identification of biomarkers associated with pediatric asthma using machine learning algorithms: a review
topic 6200
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10681392/
https://www.ncbi.nlm.nih.gov/pubmed/38013370
http://dx.doi.org/10.1097/MD.0000000000036070
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