Evidence map›Paper›PMID 32596378›Full record

ArticleBioMed research international2020

Two Gene Set Variation Index as Biomarker of Bacterial and Fungal Sepsis.

Xiaowen Zheng, Yifeng Luo, Qian Li, Jihua Feng, Chunling Zhao, Junyu Lu, Jiefeng Luo, Jianfeng Zhang

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Xiaowen ZhengDepartment of Emergency Medicine, The Second Affiliated Hospital of Guangxi Medical University, Nanning 530007, China.
Yifeng LuoDepartment of Emergency Medicine, The Second Affiliated Hospital of Guangxi Medical University, Nanning 530007, China.
Qian LiDepartment of Emergency Medicine, The Second Affiliated Hospital of Guangxi Medical University, Nanning 530007, China.
Jihua FengDepartment of Emergency Medicine, The Second Affiliated Hospital of Guangxi Medical University, Nanning 530007, China.
Chunling ZhaoDepartment of Emergency Medicine, The Second Affiliated Hospital of Guangxi Medical University, Nanning 530007, China.
Junyu LuDepartment of Emergency Medicine, The Second Affiliated Hospital of Guangxi Medical University, Nanning 530007, China.
Jiefeng LuoDepartment of Emergency Medicine, The Second Affiliated Hospital of Guangxi Medical University, Nanning 530007, China.ORCID https://orcid.org/0000-0002-4792-0176
Jianfeng ZhangDepartment of Emergency Medicine, The Second Affiliated Hospital of Guangxi Medical University, Nanning 530007, China.ORCID https://orcid.org/0000-0003-4213-9310
Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe incidence of sepsis has been increasing in recent years. The molecular mechanism of different pathogenic sepsis remains elusive, and biomarkers of sepsis against different pathogens are still lacking.

methodsThe microarray data of bacterial sepsis, fungal sepsis, and mock-treated samples were applied to perform differentially expressed gene (DEG) analysis to identify a bacterial sepsis-specific gene set and a fungal sepsis-specific gene set. Functional enrichment analysis was used to explore the body's response to bacterial sepsis and fungal sepsis. Gene set variation analysis (GSVA) was used to score individual samples against the two pathogen-specific gene sets, and each sample gets a GSVA index. Receiver operating characteristic (ROC) curve analysis was performed to evaluate the diagnostic value of sepsis. An independent data set was used to validate the bacterial sepsis-specific GSVA index.

resultsThe genes differentially expressed only in bacterial sepsis and the genes differentially expressed only in fungal sepsis were significantly involved in different biological processes (BPs) and pathways. This indicated that the body's responses to fungal sepsis and bacterial sepsis are varied. Twenty-two genes were identified as bacterial sepsis-specific genes and upregulated in bacterial sepsis, and 23 genes were identified as fungal sepsis-specific genes and upregulated in fungal sepsis. ROC curve analysis showed that both of the two pathogen sepsis-specific GSVA indexes may be a reliable biomarker for corresponding pathogen-induced sepsis (AUC = 1.000), while the mRNA of CALCA (also known as PCT) have a poor diagnostic value with AUC = 0.512 in bacterial sepsis and AUC = 0.705 in fungi sepsis. In addition, the AUC of the bacterial sepsis-specific GSVA index in the independent data set was 0.762.

conclusionWe proposed a bacterial sepsis-specific gene set and a fungal sepsis-specific gene set; the bacterial sepsis GSVA index may be a reliable biomarker for bacterial sepsis.

Indexed as

BacteremiaFungemiaTranscriptomeBiomarkersCalcitonin Gene-Related PeptideHumansROC CurveBiomarkersCALCA protein, humanCalcitonin Gene-Related Peptide

Identifiers

PMID32596378
PMCPMC7292977
OpenAlexW3034076793

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.