Evidence map›Paper›PMID 41345254›Full record

ArticleScientific reports2025

Bioinformatics analysis of immune-related differentially expressed genes in Kawasaki disease.

Mengjia Zhao, Ruihua Yang

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Mengjia ZhaoDepartment of Cardiovascular, Rheumatology and Immunology, Shanxi Children's Hospital, No. 65, Jinxi Street, Jinyuan District, Taiyuan, 030000, Shanxi, China.
Ruihua YangDepartment of Cardiovascular, Rheumatology and Immunology, Shanxi Children's Hospital, Taiyuan, 030000, China. yangruihua0339@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kawasaki disease (KD) is an acute pediatric systemic vasculitis of unknown origin, where emerging evidence suggests that immune dysregulation and alterations in peripheral immune cell populations play critical roles in its pathogenesis. In this study, we performed comprehensive bioinformatics analyses to identify KD-associated genes and develop an accurate diagnostic model for early detection. Two publicly available microarray datasets, GSE73461 (132 samples) and GSE68004 (126 samples), were obtained from the Gene Expression Omnibus database and analyzed. Immune-related differentially expressed genes (IMRDEGs) were identified by integrating differential expression profiling with Gene Ontology annotation and Kyoto Encyclopedia of Genes and Genomes pathway analysis. To select optimal biomarkers, we employed a multi-algorithm framework combining logistic regression, SVM-RFE, and LASSO regression. Among 12 IMRDEGs identified, five genes (ITGAM, CAMP, CD4, IL2RB, and IL1B) were identified as having potential diagnostic value, with ITGAM showing the strongest predictive value. Functional enrichment revealed these genes' involvement in leukocyte activation and immune-related signaling pathways, including tuberculosis signaling. Comparative immune profiling highlighted significant differences in 14 immune cell populations between KD patients and healthy controls. Overall, our findings uncover critical immune-related genes linked to KD pathogenesis and propose a robust diagnostic model with promising clinical applicability.

Indexed as

Computational BiologyGene Expression RegulationMucocutaneous Lymph Node SyndromeBiomarkersDatabases, GeneticGene Expression ProfilingGene OntologyHumansTranscriptomeBiomarkersBioinformaticsImmune-related differentially expressed genesKawasaki disease

Identifiers

PMID41345254
PMCPMC12783145

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.