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pmid:37867954

Identification of immune-related genes for the diagnosis of ischemic heart failure based on bioinformatics.

Yiding Yu · Xiujuan Liu · Yitao Xue · Yan Li

iScience · 2023 doi:10.1016/j.isci.2023.108121

Paper

complete

Experiment

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Data

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Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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title
Identification of immune-related genes for the diagnosis of ischemic heart failure based on bioinformatics.
doi
10.1016/j.isci.2023.108121
pmid
37867954
authors array · 4 items
[0]
Yiding Yu
[1]
Xiujuan Liu
[2]
Yitao Xue
[3]
Yan Li
journal
iScience
year
2023
abstract
The role of immune cells in the pathogenesis of ischemic heart failure (IHF) is well-established. However, identifying key genes in patients with IHF remains a challenge. We obtained two IHF datasets from the GEO database (GSE76701 and GSE21610), and identified four potential diagnostic candidate genes for IHF by using bioinformatics and machine learning algorithms, namely RNASE2, MFAP4, CHRDL1, and KCNN3. We constructed nomogram and validated the diagnostic value of these genes on additional GEO datasets (GSE57338). The results showed that these four genes had high diagnostic value (area under the curve value of 0.961). Furthermore, our immune infiltration analysis revealed the presence of three dysregulated immune cells in IHF, namely macrophages M2, monocytes, and T cells gamma delta. We also explored the potential molecular mechanisms of IHF. These findings provide new insights into the pathogenesis, diagnosis, and treatment of IHF.
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To gain insights into the differences between heart failure and normal samples, we employed the limma package and identified genes with adjust p values <0.05 and | log2(FC)| ≥ 1 as the difference genes.
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sections[19] "Data processing and differentially expressed gene screening" paragraph 2
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To gain insights into the differences between heart failure and normal samples, we employed the limma package and identified genes with adjust p values <0.05 and | log2(FC)| ≥ 1 as the difference genes.
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This study analyzes existing, publicly available data. The sources for the datasets are listed in the key resources table.
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The validation results showed that the area under the curve (AUC) of each gene was greater than 0.7, and the AUC of the 4-gene diagnostic model was 0.961, which had high diagnostic value.
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sections[7] "Diagnostic value assessment" paragraph 2
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The validation results showed that the area under the curve (AUC) of each gene was greater than 0.7, and the AUC of the 4-gene diagnostic model was 0.961, which had high diagnostic value.
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The validation results showed that the area under the curve (AUC) of each gene was greater than 0.7, and the AUC of the 4-gene diagnostic model was 0.961, which had high diagnostic value.
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label
Principal component analysis
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wide_numeric_matrix
evidence object · 3 fields
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0.8
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high
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PCA
[2] object · 10 fields
id
method-3
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network_analysis
specific
pathway_enrichment
label
Network / pathway analysis
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pathway_enrich
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evidence object · 3 fields
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0.8
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GO enrichment
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method.reader_differs_from_extractor
capability object · 3 fields
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complete
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capability:computational_analysis
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[4]
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[5]
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[6]
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[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
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complete
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fdr_bh
missing_operations array · 0 items
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: limma_voom.
capability object · 4 fields
tier
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capability:computational_analysis
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The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
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GSE76701
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GSE21610
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GSE76701
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GSE57338
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[0]
This study analyzes existing, publicly available data. The sources for the datasets are listed in the key resources table.
basis
The paper names GSE21610, GSE76701, GSE57338 in GEO and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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data:geo:GSE21610
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review object · 5 fields
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partial
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reader object · 5 fields
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MiniMax-M3.1-Flash
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minimax
provider_family
minimax
read_at
2026-11-01T18:56:48Z
independence
single_reader
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verbatim
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9768
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pmid:37867954
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paper
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PMID 37867954 full text
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GEO GSE21610
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PMID 37867954 full text
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dataset
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GEO GSE21610
agent
agent:corpus-assay-engine
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erally up-regulated, while genes involved in apoptosis, proteasome, and Th1 and Th2 cell differenti
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To gain insights into the differences between heart failure and normal samples, we employed the limma package and identified genes with adjust p values <0.05 and | log2(FC)| ≥ 1 as the difference genes.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37867954", "kind": "science-record", "revision": 4, "content_hash": "sha256:c1f8c2fa4530f539c3f94525cbe2fe7bbd9f2aac8f8e24ecdb819a7dd78c13a6", "created_at": "2026-11-01T19:02:43Z", "updated_at": "2026-11-01T22:52:55Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of immune-related genes for the diagnosis of ischemic heart failure based on bioinformatics.", "doi": "10.1016/j.isci.2023.108121", "pmid": "37867954", "authors": ["Yiding Yu", "Xiujuan Liu", "Yitao Xue", "Yan Li"], "journal": "iScience", "year": 2023, "abstract": "The role of immune cells in the pathogenesis of ischemic heart failure (IHF) is well-established. However, identifying key genes in patients with IHF remains a challenge. We obtained two IHF datasets from the GEO database (GSE76701 and GSE21610), and identified four potential diagnostic candidate genes for IHF by using bioinformatics and machine learning algorithms, namely RNASE2, MFAP4, CHRDL1, and KCNN3. We constructed nomogram and validated the diagnostic value of these genes on additional GEO datasets (GSE57338). The results showed that these four genes had high diagnostic value (area under the curve value of 0.961). Furthermore, our immune infiltration analysis revealed the presence of three dysregulated immune cells in IHF, namely macrophages M2, monocytes, and T cells gamma delta. We also explored the potential molecular mechanisms of IHF. These findings provide new insights into the pathogenesis, diagnosis, and treatment of IHF.", "claims": [{"id": "claim-method", "statement": "To gain insights into the differences between heart failure and normal samples, we employed the limma package and identified genes with adjust p values <0.05 and | log2(FC)| ≥ 1 as the difference genes.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37867954", "locator": "sections[19] \"Data processing and differentially expressed gene screening\" paragraph 2", "quote": "To gain insights into the differences between heart failure and normal samples, we employed the limma package and identified genes with adjust p values <0.05 and | log2(FC)| ≥ 1 as the difference genes."}], "state": "complete"}, {"id": "claim-data-access", "statement": "This study analyzes existing, publicly available data. 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