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pmid:36266609

Integrative analyses of immune-related biomarkers and associated mechanisms in coronary heart disease.

Lianbo Zhang · Guibin Li · Bo Liang · Xiaoli Su · Haolin Xie · Hongxia Sun · Ge Wu

BMC medical genomics · 2022 doi:10.1186/s12920-022-01375-w

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complete

Experiment

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Data

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title
Integrative analyses of immune-related biomarkers and associated mechanisms in coronary heart disease.
doi
10.1186/s12920-022-01375-w
pmid
36266609
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[0]
Lianbo Zhang
[1]
Guibin Li
[2]
Bo Liang
[3]
Xiaoli Su
[4]
Haolin Xie
[5]
Hongxia Sun
[6]
Ge Wu
journal
BMC medical genomics
year
2022
abstract
Various studies showed that the effect of immune activation is pro-atherogenic and coronary heart disease (CHD) should therefore be considered an autoimmune disease. This study aimed to identify potential immune-related biomarkers, pathways, and the potential regulatory networks underlying CHD. Differentially expressed genes (DEGs) between CHD and control samples were determined by analyzing GSE71226 and GSE9128. The overlapping differential expression immune-related genes (DE-IRGs) for CHD were identified by analyzing the ImmPort database and two GEO databases. A total of 384 DE-IRGs were identified. Subsequently, comprehensive enrichment analyses suggested that DE-IRGs were enriched in immune-related pathways, including autoimmune thyroid disease, the intestinal immune network for IGA production, and downstream signaling events of B cell receptors. The signature of DE-IRGs was validated using an external independent dataset GSE20681 (AUC = 0.875). Furthermore, we conducted protein-protein interaction network analysis and identified eight hub genes, which were most enriched in regulation of defense response, NF-κB signaling pathway, regulation of JNK cascade, and regulation of cytokine production. Moreover, networks of miRNAs-mRNAs and transcription factors (TFs)-mRNA underlying the integrated data were established, involving eight miRNAs and 76 TF-targeting hub genes. Ultimately, 17 SNPs in miRNA-mediated gene networks were identified. We screened potential immune-related genes in CHD and constructed miRNA-mRNA-TF and SNP-miRNA networks, which not only provide inspired insights into the occurrence and the molecular mechanisms of CHD but also lay a foundation for targeting potential biomarkers using immunotherapy and for understanding the molecular mechanisms of CHD.
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We screened the DEGs from two GEO datasets using the limma package, with the threshold criterion of |log2FC|> 1 and adj. p value < 0.05.
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We screened the DEGs from two GEO datasets using the limma package, with the threshold criterion of |log2FC|> 1 and adj. p value < 0.05.
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All data generated or analyzed during this study are included in this published article and its supplementary information files. The datasets generated and/or analysed during the current study are available in the GEO repository, https://www.ncbi.nlm.nih.gov/geo/.
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A total of 348 overlapping DE-IRGs, the intersection of DEGs and ImmPort genes, were identified.
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A total of 348 overlapping DE-IRGs (Fig. 3C), the intersection of DEGs and ImmPort genes, integrated by the Venn Diagram online tool were identified (Fig. 3C).
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The overlapping differential expression immune-related genes (DE-IRGs) for CHD were identified by analyzing the ImmPort database and two GEO databases.
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Whole Blood Cell Gene Expression Profiling in Patients with Coronary Artery Disease from the PREDICT Trial
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GEO GSE20681
activities array · 3 items
[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
used array · 3 items
[0] object · 3 fields
id
pmid:36266609
type
paper
label
pmid:36266609
[1] object · 3 fields
id
source:pmid:36266609
type
manuscript
label
PMID 36266609 full text
[2] object · 3 fields
id
data:geo:GSE20681
type
dataset
label
GEO GSE20681
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-36266609
type
extraction
used array · 1 item
[0]
source:pmid:36266609
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE20681
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE20681
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
type
software
label
Corpus assay engine
[1] object · 3 fields
id
agent:minimax-reader
type
software
label
MiniMax literature reader
source_run_id
reading-sci-2026-11-01
dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
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snapshot_id
ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:36266609
parent_hash
sha256:869aa1a2733cd658711b5392c540bb07dff8e8033a530afda71f7bb8026e6c04
fork_of
null
gaps array · 10 items
[0]
asset:data:geo:GSE20681 licence not read
[1]
asset:data:geo:GSE20681 not downloaded
[2]
asset:data:geo:GSE71226 licence not read
[3]
asset:data:geo:GSE71226 not downloaded
[4]
asset:data:geo:GSE9128 licence not read
[5]
asset:data:geo:GSE9128 not downloaded
[6]
execution.not_run
[7]
review.human_critique
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review.independent_reader
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review.machine_critique
assays array · 1 item
[0] object · 11 fields
role
analysis
definition_id
differential_expression
definition_version
f2132e96ae6c7a4e
required_operations array · 3 items
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normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
We screened the DEGs from two GEO datasets using the limma package, with the threshold criterion of |log2FC|> 1 and adj. p value < 0.05.
order_basis
analysis_only
id
assay:1
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36266609", "kind": "science-record", "revision": 5, "content_hash": "sha256:abf620e56dbc8a27ab1aa9d95bdd849861de9e9060c7563482b4d55471ec0056", "created_at": "2026-11-01T18:15:39Z", "updated_at": "2026-11-01T22:50:25Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Integrative analyses of immune-related biomarkers and associated mechanisms in coronary heart disease.", "doi": "10.1186/s12920-022-01375-w", "pmid": "36266609", "authors": ["Lianbo Zhang", "Guibin Li", "Bo Liang", "Xiaoli Su", "Haolin Xie", "Hongxia Sun", "Ge Wu"], "journal": "BMC medical genomics", "year": 2022, "abstract": "Various studies showed that the effect of immune activation is pro-atherogenic and coronary heart disease (CHD) should therefore be considered an autoimmune disease. This study aimed to identify potential immune-related biomarkers, pathways, and the potential regulatory networks underlying CHD. Differentially expressed genes (DEGs) between CHD and control samples were determined by analyzing GSE71226 and GSE9128. The overlapping differential expression immune-related genes (DE-IRGs) for CHD were identified by analyzing the ImmPort database and two GEO databases. A total of 384 DE-IRGs were identified. Subsequently, comprehensive enrichment analyses suggested that DE-IRGs were enriched in immune-related pathways, including autoimmune thyroid disease, the intestinal immune network for IGA production, and downstream signaling events of B cell receptors. The signature of DE-IRGs was validated using an external independent dataset GSE20681 (AUC = 0.875). Furthermore, we conducted protein-protein interaction network analysis and identified eight hub genes, which were most enriched in regulation of defense response, NF-κB signaling pathway, regulation of JNK cascade, and regulation of cytokine production. Moreover, networks of miRNAs-mRNAs and transcription factors (TFs)-mRNA underlying the integrated data were established, involving eight miRNAs and 76 TF-targeting hub genes. Ultimately, 17 SNPs in miRNA-mediated gene networks were identified. We screened potential immune-related genes in CHD and constructed miRNA-mRNA-TF and SNP-miRNA networks, which not only provide inspired insights into the occurrence and the molecular mechanisms of CHD but also lay a foundation for targeting potential biomarkers using immunotherapy and for understanding the molecular mechanisms of CHD.", "claims": [{"id": "claim-method", "statement": "We screened the DEGs from two GEO datasets using the limma package, with the threshold criterion of |log2FC|> 1 and adj. p value < 0.05.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36266609", "locator": "sections[4] \"Identification of differentially expressed immune-related genes (DE-IRGs)\" paragraph 2", "quote": "We screened the DEGs from two GEO datasets using the limma package, with the threshold criterion of |log2FC|> 1 and adj. p value < 0.05."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All data generated or analyzed during this study are included in this published article and its supplementary information files. 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This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE20681"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE20681"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:36266609", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1186/s12920-022-01375-w", "sha256": "sha256:68477c268f7930facbf9a3d4c80ec854a548f9f7494b41f25524c3a25298cbda", "bytes": 50380, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1186/s12920-022-01375-w", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC9585797", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE20681", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE20681", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE20681", "version": null, "note": "All data generated or analyzed during this study are included in this published article and its supplementary information files. 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