Evidence map›Paper›PMID 35844622›Full record

ArticleFrontiers in immunology2022

Integrated Analysis of Gene Co-Expression Network and Prediction Model Indicates Immune-Related Roles of the Identified Biomarkers in Sepsis and Sepsis-Induced Acute Respiratory Distress Syndrome.

Tingqian Ming, Mingyou Dong, Xuemin Song, Xingqiao Li, Qian Kong, Qing Fang, Jie Wang, Xiaojing Wu, Zhongyuan Xia

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 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Identification of CD19Journal of inflammation research · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
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  13. Classification of subtypes and identification of dysregulated genes in sepsis.Frontiers in cellular and infection microbiology · 2023
    Article
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  15. 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 1 country.

Tingqian MingDepartment of Anesthesiology, Renmin Hospital, Wuhan University, Wuhan, China.
Mingyou DongCollege of Medical Laboratory Science, Youjiang Medical College for Nationalities, Baise, China.
Xuemin SongDepartment of Anesthesiology and Critical Care Medicine, Zhongnan Hospital, Wuhan University, Wuhan, China.
Xingqiao LiSchool of Computer, Wuhan University, Wuhan, China.
Qian KongDepartment of Anesthesiology, Renmin Hospital, Wuhan University, Wuhan, China.
Qing FangDepartment of Anesthesiology and Critical Care Medicine, Zhongnan Hospital, Wuhan University, Wuhan, China.
Jie WangDepartment of Otolaryngology-Head and Neck Surgery, Renmin Hospital, Wuhan University, Wuhan, China.
Xiaojing WuDepartment of Anesthesiology, Renmin Hospital, Wuhan University, Wuhan, China.
Zhongyuan XiaDepartment of Anesthesiology, Renmin Hospital, Wuhan University, Wuhan, China.
Wuhan University · CNRenmin Hospital of Wuhan University · CNYoujiang Medical College for Nationalities · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis is a series of clinical syndromes caused by immunological response to severe infection. As the most important and common complication of sepsis, acute respiratory distress syndrome (ARDS) is associated with poor outcomes and high medical expenses. However, well-described studies of analysis-based researches, especially related bioinformatics analysis on revealing specific targets and underlying molecular mechanisms of sepsis and sepsis-induced ARDS (sepsis/se-ARDS), still remain limited and delayed despite the era of data-driven medicine. In this report, weight gene co-expression network based on data from a public database was constructed to identify the key modules and screen the hub genes. Functional annotation by enrichment analysis of the modular genes also demonstrated the key biological processes and signaling pathway; among which, extensive immune-involved enrichment was remarkably associated with sepsis/se-ARDS. Based on the differential expression analysis, least absolute shrink and selection operator, and multivariable logistic regression analysis of the screened hub genes,

Indexed as

Respiratory Distress SyndromeSepsisAntigens, CDBiomarkersGene Regulatory NetworksHumansNeutrophilsReceptors, GABASialic Acid Binding Immunoglobulin-like LectinsAntigens, CDBiomarkersReceptors, GABASialic Acid Binding Immunoglobulin-like LectinsSIGLEC9 protein, humanTSPO protein, humanARDSdiagnostic biomarkergene co-expression network analysisimmune cell infiltrationprediction modelsepsis

Identifiers

PMID35844622
PMCPMC9281548
OpenAlexW4283759638

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.