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Bioinformatics Analysis of Gene Expression Profiles for Risk Prediction in Patients with Septic Shock

BACKGROUND: Septic shock occurs when sepsis is associated with critically low blood pressure, and has a high mortality rate. This study aimed to undertake a bioinformatics analysis of gene expression profiles for risk prediction in septic shock. MATERIAL/METHODS: Two good quality datasets associated...

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Autores principales: Hu, Yingchun, Cheng, Lingxia, Zhong, Wu, Chen, Muhu, Zhang, Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929537/
https://www.ncbi.nlm.nih.gov/pubmed/31838482
http://dx.doi.org/10.12659/MSM.918491
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author Hu, Yingchun
Cheng, Lingxia
Zhong, Wu
Chen, Muhu
Zhang, Qian
author_facet Hu, Yingchun
Cheng, Lingxia
Zhong, Wu
Chen, Muhu
Zhang, Qian
author_sort Hu, Yingchun
collection PubMed
description BACKGROUND: Septic shock occurs when sepsis is associated with critically low blood pressure, and has a high mortality rate. This study aimed to undertake a bioinformatics analysis of gene expression profiles for risk prediction in septic shock. MATERIAL/METHODS: Two good quality datasets associated with septic shock were downloaded from the Gene Expression Omnibus (GEO) database, GSE64457 and GSE57065. Patients with septic shock had both sepsis and hypotension, and a normal control group was included. The differentially expressed genes (DEGs) were identified using OmicShare tools based on R. Functional enrichment of DEGs was analyzed using DAVID. The protein-protein interaction (PPI) network was established using STRING. Survival curves of key genes were constructed using GraphPad Prism version 7.0. Each putative central gene was analyzed by receiver operating characteristic (ROC) curves using MedCalc statistical software. RESULTS: GSE64457 and GSE57065 included 130 RNA samples derived from whole blood from 97 patients with septic shock and 33 healthy volunteers to obtain 975 DEGs, 455 of which were significantly down-regulated and 520 were significantly upregulated (P<0.05). Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis identified significantly enriched DEGs in four signaling pathways, MAPK, TNF, HIF-1, and insulin. Six genes, WDR82, ASH1L, NCOA1, TPR, SF1, and CREBBP in the center of the PPI network were associated with septic shock, according to survival curve and ROC analysis. CONCLUSIONS: Bioinformatics analysis of gene expression profiles identified four signaling pathways and six genes, potentially representing molecular mechanisms for the occurrence, progression, and risk prediction in septic shock.
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spelling pubmed-69295372019-12-26 Bioinformatics Analysis of Gene Expression Profiles for Risk Prediction in Patients with Septic Shock Hu, Yingchun Cheng, Lingxia Zhong, Wu Chen, Muhu Zhang, Qian Med Sci Monit Lab/In Vitro Research BACKGROUND: Septic shock occurs when sepsis is associated with critically low blood pressure, and has a high mortality rate. This study aimed to undertake a bioinformatics analysis of gene expression profiles for risk prediction in septic shock. MATERIAL/METHODS: Two good quality datasets associated with septic shock were downloaded from the Gene Expression Omnibus (GEO) database, GSE64457 and GSE57065. Patients with septic shock had both sepsis and hypotension, and a normal control group was included. The differentially expressed genes (DEGs) were identified using OmicShare tools based on R. Functional enrichment of DEGs was analyzed using DAVID. The protein-protein interaction (PPI) network was established using STRING. Survival curves of key genes were constructed using GraphPad Prism version 7.0. Each putative central gene was analyzed by receiver operating characteristic (ROC) curves using MedCalc statistical software. RESULTS: GSE64457 and GSE57065 included 130 RNA samples derived from whole blood from 97 patients with septic shock and 33 healthy volunteers to obtain 975 DEGs, 455 of which were significantly down-regulated and 520 were significantly upregulated (P<0.05). Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis identified significantly enriched DEGs in four signaling pathways, MAPK, TNF, HIF-1, and insulin. Six genes, WDR82, ASH1L, NCOA1, TPR, SF1, and CREBBP in the center of the PPI network were associated with septic shock, according to survival curve and ROC analysis. CONCLUSIONS: Bioinformatics analysis of gene expression profiles identified four signaling pathways and six genes, potentially representing molecular mechanisms for the occurrence, progression, and risk prediction in septic shock. International Scientific Literature, Inc. 2019-12-15 /pmc/articles/PMC6929537/ /pubmed/31838482 http://dx.doi.org/10.12659/MSM.918491 Text en © Med Sci Monit, 2019 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Lab/In Vitro Research
Hu, Yingchun
Cheng, Lingxia
Zhong, Wu
Chen, Muhu
Zhang, Qian
Bioinformatics Analysis of Gene Expression Profiles for Risk Prediction in Patients with Septic Shock
title Bioinformatics Analysis of Gene Expression Profiles for Risk Prediction in Patients with Septic Shock
title_full Bioinformatics Analysis of Gene Expression Profiles for Risk Prediction in Patients with Septic Shock
title_fullStr Bioinformatics Analysis of Gene Expression Profiles for Risk Prediction in Patients with Septic Shock
title_full_unstemmed Bioinformatics Analysis of Gene Expression Profiles for Risk Prediction in Patients with Septic Shock
title_short Bioinformatics Analysis of Gene Expression Profiles for Risk Prediction in Patients with Septic Shock
title_sort bioinformatics analysis of gene expression profiles for risk prediction in patients with septic shock
topic Lab/In Vitro Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929537/
https://www.ncbi.nlm.nih.gov/pubmed/31838482
http://dx.doi.org/10.12659/MSM.918491
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