Cargando…
Identification of crucial genes related to heart failure based on GEO database
BACKGROUND: The molecular biological mechanisms underlying heart failure (HF) remain poorly understood. Therefore, it is imperative to use innovative approaches, such as high-throughput sequencing and artificial intelligence, to investigate the pathogenesis, diagnosis, and potential treatment of HF....
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10385922/ https://www.ncbi.nlm.nih.gov/pubmed/37507655 http://dx.doi.org/10.1186/s12872-023-03400-x |
_version_ | 1785081532558344192 |
---|---|
author | Chen, Yongliang Xue, Jing Yan, Xiaoli Fang, Da-guang Li, Fangliang Tian, Xuefei Yan, Peng Feng, Zengbin |
author_facet | Chen, Yongliang Xue, Jing Yan, Xiaoli Fang, Da-guang Li, Fangliang Tian, Xuefei Yan, Peng Feng, Zengbin |
author_sort | Chen, Yongliang |
collection | PubMed |
description | BACKGROUND: The molecular biological mechanisms underlying heart failure (HF) remain poorly understood. Therefore, it is imperative to use innovative approaches, such as high-throughput sequencing and artificial intelligence, to investigate the pathogenesis, diagnosis, and potential treatment of HF. METHODS: First, we initially screened Two data sets (GSE3586 and GSE5406) from the GEO database containing HF and control samples from the GEO database to establish the Train group, and selected another dataset (GSE57345) to construct the Test group for verification. Next, we identified the genes with significantly different expression levels in patients with or without HF and performed functional and pathway enrichment analyses. HF-specific genes were identified, and an artificial neural network was constructed by Random Forest. The ROC curve was used to evaluate the accuracy and reliability of the constructed model in the Train and Test groups. Finally, immune cell infiltration was analyzed to determine the role of the inflammatory response and the immunological microenvironment in the pathogenesis of HF. RESULTS: In the Train group, 153 significant differentially expressed genes (DEGs) associated with HF were found to be abnormal, including 81 down-regulated genes and 72 up-regulated genes. GO and KEGG enrichment analyses revealed that the down-regulated genes were primarily enriched in organic anion transport, neutrophil activation, and the PI3K-Akt signaling pathway. The upregulated genes were mainly enriched in neutrophil activation and the calcium signaling. DEGs were identified using Random Forest, and finally, 16 HF-specific genes were obtained. In the ROC validation and evaluation, the area under the curve (AUC) of the Train and Test groups were 0.996 and 0.863, respectively. CONCLUSIONS: Our research revealed the potential functions and pathways implicated in the progression of HF, and designed an RNA diagnostic model for HF tissues using machine learning and artificial neural networks. Sensitivity, specificity, and stability were confirmed by ROC curves in the two different cohorts. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-023-03400-x. |
format | Online Article Text |
id | pubmed-10385922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103859222023-07-30 Identification of crucial genes related to heart failure based on GEO database Chen, Yongliang Xue, Jing Yan, Xiaoli Fang, Da-guang Li, Fangliang Tian, Xuefei Yan, Peng Feng, Zengbin BMC Cardiovasc Disord Research BACKGROUND: The molecular biological mechanisms underlying heart failure (HF) remain poorly understood. Therefore, it is imperative to use innovative approaches, such as high-throughput sequencing and artificial intelligence, to investigate the pathogenesis, diagnosis, and potential treatment of HF. METHODS: First, we initially screened Two data sets (GSE3586 and GSE5406) from the GEO database containing HF and control samples from the GEO database to establish the Train group, and selected another dataset (GSE57345) to construct the Test group for verification. Next, we identified the genes with significantly different expression levels in patients with or without HF and performed functional and pathway enrichment analyses. HF-specific genes were identified, and an artificial neural network was constructed by Random Forest. The ROC curve was used to evaluate the accuracy and reliability of the constructed model in the Train and Test groups. Finally, immune cell infiltration was analyzed to determine the role of the inflammatory response and the immunological microenvironment in the pathogenesis of HF. RESULTS: In the Train group, 153 significant differentially expressed genes (DEGs) associated with HF were found to be abnormal, including 81 down-regulated genes and 72 up-regulated genes. GO and KEGG enrichment analyses revealed that the down-regulated genes were primarily enriched in organic anion transport, neutrophil activation, and the PI3K-Akt signaling pathway. The upregulated genes were mainly enriched in neutrophil activation and the calcium signaling. DEGs were identified using Random Forest, and finally, 16 HF-specific genes were obtained. In the ROC validation and evaluation, the area under the curve (AUC) of the Train and Test groups were 0.996 and 0.863, respectively. CONCLUSIONS: Our research revealed the potential functions and pathways implicated in the progression of HF, and designed an RNA diagnostic model for HF tissues using machine learning and artificial neural networks. Sensitivity, specificity, and stability were confirmed by ROC curves in the two different cohorts. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-023-03400-x. BioMed Central 2023-07-28 /pmc/articles/PMC10385922/ /pubmed/37507655 http://dx.doi.org/10.1186/s12872-023-03400-x 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Chen, Yongliang Xue, Jing Yan, Xiaoli Fang, Da-guang Li, Fangliang Tian, Xuefei Yan, Peng Feng, Zengbin Identification of crucial genes related to heart failure based on GEO database |
title | Identification of crucial genes related to heart failure based on GEO database |
title_full | Identification of crucial genes related to heart failure based on GEO database |
title_fullStr | Identification of crucial genes related to heart failure based on GEO database |
title_full_unstemmed | Identification of crucial genes related to heart failure based on GEO database |
title_short | Identification of crucial genes related to heart failure based on GEO database |
title_sort | identification of crucial genes related to heart failure based on geo database |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10385922/ https://www.ncbi.nlm.nih.gov/pubmed/37507655 http://dx.doi.org/10.1186/s12872-023-03400-x |
work_keys_str_mv | AT chenyongliang identificationofcrucialgenesrelatedtoheartfailurebasedongeodatabase AT xuejing identificationofcrucialgenesrelatedtoheartfailurebasedongeodatabase AT yanxiaoli identificationofcrucialgenesrelatedtoheartfailurebasedongeodatabase AT fangdaguang identificationofcrucialgenesrelatedtoheartfailurebasedongeodatabase AT lifangliang identificationofcrucialgenesrelatedtoheartfailurebasedongeodatabase AT tianxuefei identificationofcrucialgenesrelatedtoheartfailurebasedongeodatabase AT yanpeng identificationofcrucialgenesrelatedtoheartfailurebasedongeodatabase AT fengzengbin identificationofcrucialgenesrelatedtoheartfailurebasedongeodatabase |