Evidence map›Paper›PMID 37398680›Full record

ArticleFrontiers in immunology2023

Identification and validation of a novel mitochondrion-related gene signature for diagnosis and immune infiltration in sepsis.

Shuai Hao, Miao Huang, Xiaofan Xu, Xulin Wang, Yuqing Song, Wendi Jiang, Liqun Huo, Jun Gu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.2field-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

12 citing papers in PubMed, 15 citations in OpenAlex.

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  6. Review
  7. Revealing Cell-Free Mitochondrial DNA Breakage Patterns as Novel Biomarkers for Sepsis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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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 3 institutions in 1 country.

Shuai HaoDepartment of General Surgery, Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Miao HuangNursing School, Chongqing Medical University, Chongqing, China.
Xiaofan XuDepartment of General Surgery, Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Xulin WangDepartment of General Surgery, Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Yuqing SongDepartment of General Surgery, Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Wendi JiangDepartment of General Surgery, Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Liqun HuoDepartment of General Surgery, Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Jun GuDepartment of General Surgery, Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Nanjing General Hospital of Nanjing Military Command · CNNanjing University · CNChongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Owing to the complex pathophysiological features and heterogeneity of sepsis, current diagnostic methods are not sufficiently precise or timely, causing a delay in treatment. It has been suggested that mitochondrial dysfunction plays a critical role in sepsis. However, the role and mechanism of mitochondria-related genes in the diagnostic and immune microenvironment of sepsis have not been sufficiently investigated. Methods: Mitochondria-related differentially expressed genes (DEGs) were identified between human sepsis and normal samples from GSE65682 dataset. Least absolute shrinkage and selection operator (LASSO) regression and the Support Vector Machine (SVM) analyses were carried out to locate potential diagnostic biomarkers. Gene ontology and gene set enrichment analyses were conducted to identify the key signaling pathways associated with these biomarker genes. Furthermore, correlation of these genes with the proportion of infiltrating immune cells was estimated using CIBERSORT. The expression and diagnostic value of the diagnostic genes were evaluated using GSE9960 and GSE134347 datasets and septic patients. Furthermore, we established an Results: In this study, 647 mitochondrion-related DEGs were obtained. Machine learning confirmed six critical mitochondrion-related DEGs, including Conclusion: We constructed a novel diagnostic model containing six MRGs, which has the potential to be an innovative tool for the early diagnosis of sepsis.

Indexed as

MitochondriaSepsisArea Under CurveDNA, MitochondrialGene OntologyHumansLipopolysaccharidesDNA, MitochondrialLipopolysaccharidesbioinformaticsdiagnostic biomarkersimmune infiltrationmitochondrionsepsis

Identifiers

PMID37398680
PMCPMC10310918
OpenAlexW4380680794

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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.