Evidence map›Paper›PMID 36203606›Full record

ArticleFrontiers in immunology2022

Identification of immune-related endoplasmic reticulum stress genes in sepsis using bioinformatics and machine learning.

Ting Gong, Yongbin Liu, Zhiyuan Tian, Min Zhang, Hejun Gao, Zhiyong Peng, Shuang Yin, Chi Wai Cheung, Youtan Liu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

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

24 citing papers in PubMed, 29 citations in OpenAlex.

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  17. Recent nanoengineered therapeutic advancements in sepsis management.Frontiers in bioengineering and biotechnology · 2024
    Review
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  19. Frontiers in immunology · 2024
    Article
  20. Article
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 at 3 institutions in 2 countries.

Ting GongDepartment of Anesthesiology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Yongbin LiuDepartment of Radiology, Huazhong University of Science and Technology Union Shenzhen Hospital, Shenzhen, China.
Zhiyuan TianDepartment of Anesthesiology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Min ZhangDepartment of Anesthesiology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Hejun GaoDepartment of Anesthesiology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Zhiyong PengDepartment of Anesthesiology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Shuang YinDepartment of Anesthesiology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Chi Wai CheungDepartment of Anesthesiology, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
Youtan LiuDepartment of Anesthesiology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Third Affiliated Hospital of Southern Medical University · CNUnion Hospital · CNChinese University of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sepsis-induced apoptosis of immune cells leads to widespread depletion of key immune effector cells. Endoplasmic reticulum (ER) stress has been implicated in the apoptotic pathway, although little is known regarding its role in sepsis-related immune cell apoptosis. The aim of this study was to develop an ER stress-related prognostic and diagnostic signature for sepsis through bioinformatics and machine learning algorithms on the basis of the differentially expressed genes (DEGs) between healthy controls and sepsis patients. Methods: The transcriptomic datasets that include gene expression profiles of sepsis patients and healthy controls were downloaded from the GEO database. The immune-related endoplasmic reticulum stress hub genes associated with sepsis patients were identified using the new comprehensive machine learning algorithm and bioinformatics analysis which includes functional enrichment analyses, consensus clustering, weighted gene coexpression network analysis (WGCNA), and protein-protein interaction (PPI) network construction. Next, the diagnostic model was established by logistic regression and the molecular subtypes of sepsis were obtained based on the significant DEGs. Finally, the potential diagnostic markers of sepsis were screened among the significant DEGs, and validated in multiple datasets. Results: Significant differences in the type and abundance of infiltrating immune cell populations were observed between the healthy control and sepsis patients. The immune-related ER stress genes achieved strong stability and high accuracy in predicting sepsis patients. 10 genes were screened as potential diagnostic markers for sepsis among the significant DEGs, and were further validated in multiple datasets. In addition, higher expression levels of SCAMP5 mRNA and protein were observed in PBMCs isolated from sepsis patients than healthy donors (n = 5). Conclusions: We established a stable and accurate signature to evaluate the diagnosis of sepsis based on the machine learning algorithms and bioinformatics. SCAMP5 was preliminarily identified as a diagnostic marker of sepsis that may affect its progression by regulating ER stress.

Indexed as

Computational BiologySepsisEndoplasmic Reticulum StressGene Expression ProfilingHumansMachine LearningMembrane ProteinsRNA, MessengerMembrane ProteinsRNA, MessengerSCAMP5 protein, humanendoplasmic reticulum stressimmunitymachine learningSCAMP5sepsis

Identifiers

PMID36203606
PMCPMC9530749
OpenAlexW4297906923

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Registered trials

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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.