Evidence map›Paper›PMID 38914792›Full record

ArticleScientific reports2024

Potential diagnostic biomarkers for immunogenic cell death in elderly female patients with ischemic stroke: identification and analysis.

Lihua Qin, Sheng Li, Xi Cao, Tengjia Huang, Yixin Liu, Ouying Chen

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Lihua Qin *School of Nursing, Hunan University of Chinese Medicine, Changsha, 410208, Hunan, People's Republic of China.
Sheng Li *Key Laboratory of Hunan Province for Prevention and Treatment of Integrated Traditional Chinese and Western Medicine On Cardiocerebral Diseases, Hunan University of Chinese Medicine, Changsha, 410208, Hunan, People's Republic of China.
Xi CaoSchool of Nursing, Hunan University of Chinese Medicine, Changsha, 410208, Hunan, People's Republic of China.
Tengjia HuangSchool of Nursing, Hunan University of Chinese Medicine, Changsha, 410208, Hunan, People's Republic of China.
Yixin LiuSchool of Nursing, Hunan University of Chinese Medicine, Changsha, 410208, Hunan, People's Republic of China.
Ouying ChenSchool of Nursing, Hunan University of Chinese Medicine, Changsha, 410208, Hunan, People's Republic of China. 003861@hnucm.edu.cn.

Funding

Disciplinary Reveal System project of Hunan University of Chinese Medicine grant number 22JBZ041Hunan Provincial Natural Science Foundation of China grant number 2023JJ50035Hunan Provincial Natural Science Foundation of China grant number 2024JJ8124Project of Hunan Provincial Administration of Traditional Chinese Medicine grant number A2024001Scientific Research Project of Hunan Provincial Health Commission grant number B202319018677the National Natural Science Foundation of China 81904180the National Natural Science Foundation of China 82374437
6 · The paper itself

Abstract

Ischemic stroke (IS) is of increasing concern given the aging population and prevalence of unhealthy lifestyles, with older females exhibiting higher susceptibility. This study aimed to identify practical diagnostic markers, develop a diagnostic model for immunogenic cell death (ICD)-associated IS, and investigate alterations in the immune environment caused by hub genes. Differentially expressed genes associated with ICD in IS were identified based on weighted gene co-expression network analysis and the identification of significant modules. Subsequently, machine learning algorithms were employed to screened hub genes, which were further assessed using Gene Ontology, Kyoto Encyclopedia of Genes and Genomes, and Gene Set Enrichment Analysis. A nomogram mode lwas then constructed for IS diagnosis, and its diagnostic value was assessed using a receiver operating characteristic curve. Finally, alterations in immune cell infiltration were assessed within patients with IS, and the pan-cancer expression patterns of hub genes were evaluated. Three hub genes associated with ICD (PDK4, CCL20, and FBL) were identified. The corresponding nomogram model for IS diagnosis could effectively identify older female patients with IS (area under the curve (AUC) = 0.9555). Overall, the three hub genes exhibit good diagnostic value (AUC > 0.8). CCL20 and FBL are significantly associated with the extent of immune cells infiltration. Moreover, a strong link exists between hub gene expression and pan-cancer prognosis. Cumulatively, these results indicate that ICD-related hub genes critically influence IS progression in older females, presenting novel diagnostic and therapeutic targets for personalized treatment.

Indexed as

Chemokine CCL20Immunogenic Cell DeathIschemic StrokeAgedAged, 80 and overBiomarkersFemaleGene Expression ProfilingGene Regulatory NetworksHumansMachine LearningNomogramsROC CurveBiomarkersCCL20 protein, humanChemokine CCL20Diagnostic biomarkersDifferentially expressed genesImmunogenic cell deathIschemic strokeOlder female patients

Identifiers

PMID38914792
PMCPMC11196739

What Socratic holds

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LicenceCC BY
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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 Socratic graph.