Evidence map›Paper›PMID 32655806›Full record

ArticleAmerican journal of translational research2020

Two gene set variation indexes as potential diagnostic tool for sepsis.

Junyu Lu, Qian Li, Zimeng Wu, Zhimei Zhong, Pan Ji, Hongyuan Li, Cuiying He, Jihua Feng, Jianfeng Zhang

Abstract read
In one paragraph

Article in American journal of translational research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

28 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Observational
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  10. Gene Expression Dysregulation in Whole Blood of Patients withInternational journal of molecular sciences · 2024
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  11. Frontiers in immunology · 2024
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  15. [Lactate-induced up-regulation of PLEKHA4 promotes proliferation and apoptosis of human glioma cells].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
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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

9 authors.

Junyu LuIntensive Care Unit, 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.
Zimeng WuDepartment of Emergency Medicine, The Second Affiliated Hospital of Guangxi Medical University Nanning 530007, China.
Zhimei ZhongDepartment of Emergency Medicine, The Second Affiliated Hospital of Guangxi Medical University Nanning 530007, China.
Pan JiDepartment of Emergency Medicine, The Second Affiliated Hospital of Guangxi Medical University Nanning 530007, China.
Hongyuan LiDepartment of Emergency Medicine, The Second Affiliated Hospital of Guangxi Medical University Nanning 530007, China.
Cuiying HeDepartment 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.
Jianfeng ZhangDepartment of Emergency Medicine, The Second Affiliated Hospital of Guangxi Medical University Nanning 530007, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate diagnosis of sepsis remains challenging, new markers or combinations of markers are urgently needed. In the present study, we screened differentially expressed genes (DEGs) between sepsis and non-sepsis blood samples across three previously published gene expression data sets. Common upregulated and downregulated DEGs were ranked according to their average functional similarity. The ten genes (OLFM4, ORM1, CEP55, S100A12, S100P, LRG1, CEACAM8, MS4A4A, PLSCR1, and IL1R2) with the largest average functional similarity among the common upregulated genes and another ten genes (THEMIS, IL2RB, CD2, IL7R, CD3E, KLRB1, PVRIG, CCRR3, TGFBR3, and PLEKHA1) with the largest average functional similarity among the common downregulated genes were separately identified as the upregulated crucial gene set and the downregulated crucial gene set. Gene set variation analysis (GSVA) was used to obtain the GSVA index of each sample against the two crucial gene sets. Both the two crucial GSVA indexes may be robust markers for sepsis with high area under ROC curve. The diagnostic utility of the upregulated GSVA index was validated in another independent data set. Functional analyses revealed several sepsis-related pathways. In conclusion, we proposed two sepsis-related gene sets across multiple data sets and created two GSVA indexes with promising diagnostic value.

Indexed as

biomarkergene set variation analysisSepsissystemic inflammatory response syndrome

Identifiers

PMID32655806
PMCPMC7344106

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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.