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pmid:38166912

Identification of potential biological processes and key genes in diabetes-related stroke through weighted gene co-expression network analysis.

Yong He · Yang Bai · Qin Huang · Jian Xia · Jie Feng

BMC medical genomics · 2024 doi:10.1186/s12920-023-01752-z

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:38166912
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science-record
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sha256:9fe250d6cabc800eb29162bae09a4803a7b5c92f2943477eeddda7c3811e52ca
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https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
created_at
2026-11-01T19:20:05Z
updated_at
2026-11-01T22:10:58Z
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paper object · 10 fields
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title
Identification of potential biological processes and key genes in diabetes-related stroke through weighted gene co-expression network analysis.
doi
10.1186/s12920-023-01752-z
pmid
38166912
authors array · 5 items
[0]
Yong He
[1]
Yang Bai
[2]
Qin Huang
[3]
Jian Xia
[4]
Jie Feng
journal
BMC medical genomics
year
2024
abstract
BACKGROUND: Type 2 diabetes mellitus (T2DM) is an established risk factor for acute ischemic stroke (AIS). Although there are reports on the correlation of diabetes and stroke, data on its pathogenesis is limited. This study aimed to explore the underlying biological mechanisms and promising intervention targets of diabetes-related stroke. METHODS: Diabetes-related datasets (GSE38642 and GSE44035) and stroke-related datasets (GSE16561 and GSE22255) were obtained from the Gene Expression omnibus (GEO) database. The key modules for stroke and diabetes were identified by weight gene co-expression network analysis (WGCNA). Gene Ontology (GO) and Kyoto Encyclopedia of Genes Genomes (KEGG) analyses were employed in the key module. Genes in stroke- and diabetes-related key modules were intersected to obtain common genes for T2DM-related stroke. In order to discover the key genes in T2DM-related stroke, the Cytoscape and protein-protein interaction (PPI) network were constructed. The key genes were functionally annotated in the Reactome database. RESULTS: By intersecting the diabetes- and stroke-related crucial modules, 24 common genes for T2DM-related stroke were identified. Metascape showed that neutrophil extracellular trap formation was primarily enriched. The hub gene was granulin precursor (GRN), which had the highest connectivity among the common genes. In addition, functional enrichment analysis indicated that GRN was involved in neutrophil degranulation, thus regulating neutrophil extracellular trap formation. CONCLUSIONS: This study firstly revealed that neutrophil extracellular trap formation may represent the common biological processes of diabetes and stroke, and GRN may be potential intervention targets for T2DM-related stroke.
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The key modules for stroke and diabetes were identified by weight gene co-expression network analysis (WGCNA).
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The key modules for stroke and diabetes were identified by weight gene co-expression network analysis (WGCNA).
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All data from the GSE38642, GSE44035, GSE16561, and GSE22255 datasets are available at the GEO database (https://www.ncbi.nlm.nih.gov/geo/).
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Intersecting the diabetes- and stroke-related crucial modules identified 24 common genes for T2DM-related stroke, with GRN identified as the hub gene.
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evidence array · 2 items
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sections[0] "Abstract" paragraph 3
quote
By intersecting the diabetes- and stroke-related crucial modules, 24 common genes for T2DM-related stroke were identified.
[1] object · 3 fields
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sections[0] "Abstract" paragraph 3
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The hub gene was granulin precursor (GRN), which had the highest connectivity among the common genes.
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complete
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Intersecting the diabetes- and stroke-related crucial modules identified 24 common genes for T2DM-related stroke, with GRN identified as the hub gene.
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the published estimate and its evidence
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All data from the GSE38642, GSE44035, GSE16561, and GSE22255 datasets are available at the GEO database (https://www.ncbi.nlm.nih.gov/geo/).
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Gene expression analysis of peripheral whole blood RNA following ischemic stroke
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All data from the GSE38642, GSE44035, GSE16561, and GSE22255 datasets are available at the GEO database (https://www.ncbi.nlm.nih.gov/geo/).
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All data from the GSE38642, GSE44035, GSE16561, and GSE22255 datasets are available at the GEO database (https://www.ncbi.nlm.nih.gov/geo/).
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Blood genomic expression profile for ischemic stroke (IS)
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All data from the GSE38642, GSE44035, GSE16561, and GSE22255 datasets are available at the GEO database (https://www.ncbi.nlm.nih.gov/geo/).
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All data from the GSE38642, GSE44035, GSE16561, and GSE22255 datasets are available at the GEO database (https://www.ncbi.nlm.nih.gov/geo/).
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Homo sapiens
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Expression data from human pancreatic islets
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2026-11-01T15:39:54Z
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6244
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Homo sapiens
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Gene expression from human pancreatic islet
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2026-11-01T15:39:54Z
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The key modules for stroke and diabetes were identified by weight gene co-expression network analysis (WGCNA).
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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
2cb3e42f047d2ecf
snapshot_id
ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:38166912
parent_hash
sha256:ae8a14894f0ce750776502f594a990040cfaabef66e323c83406e79f6b427e3c
fork_of
null
gaps array · 13 items
[0]
asset:data:geo:GSE16561 licence not read
[1]
asset:data:geo:GSE16561 not downloaded
[2]
asset:data:geo:GSE22255 licence not read
[3]
asset:data:geo:GSE22255 not downloaded
[4]
asset:data:geo:GSE38642 licence not read
[5]
asset:data:geo:GSE38642 not downloaded
[6]
asset:data:geo:GSE44035 licence not read
[7]
asset:data:geo:GSE44035 not downloaded
[8]
execution.not_run
[9]
method.reader_named_unmapped
[10]
review.human_critique
[11]
review.independent_reader
[12]
review.machine_critique
assays array · 1 item
[0] object · 11 fields
role
analysis
definition_id
network_analysis
definition_version
f2132e96ae6c7a4e
required_operations array · 3 items
[0]
build_graph
[1]
centrality_scores
[2]
pathway_enrich
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
protein-protein interaction
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:38166912", "kind": "science-record", "revision": 3, "content_hash": "sha256:9fe250d6cabc800eb29162bae09a4803a7b5c92f2943477eeddda7c3811e52ca", "created_at": "2026-11-01T19:20:05Z", "updated_at": "2026-11-01T22:10:58Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of potential biological processes and key genes in diabetes-related stroke through weighted gene co-expression network analysis.", "doi": "10.1186/s12920-023-01752-z", "pmid": "38166912", "authors": ["Yong He", "Yang Bai", "Qin Huang", "Jian Xia", "Jie Feng"], "journal": "BMC medical genomics", "year": 2024, "abstract": "BACKGROUND: Type 2 diabetes mellitus (T2DM) is an established risk factor for acute ischemic stroke (AIS). Although there are reports on the correlation of diabetes and stroke, data on its pathogenesis is limited. This study aimed to explore the underlying biological mechanisms and promising intervention targets of diabetes-related stroke.\nMETHODS: Diabetes-related datasets (GSE38642 and GSE44035) and stroke-related datasets (GSE16561 and GSE22255) were obtained from the Gene Expression omnibus (GEO) database. The key modules for stroke and diabetes were identified by weight gene co-expression network analysis (WGCNA). Gene Ontology (GO) and Kyoto Encyclopedia of Genes Genomes (KEGG) analyses were employed in the key module. Genes in stroke- and diabetes-related key modules were intersected to obtain common genes for T2DM-related stroke. In order to discover the key genes in T2DM-related stroke, the Cytoscape and protein-protein interaction (PPI) network were constructed. The key genes were functionally annotated in the Reactome database.\nRESULTS: By intersecting the diabetes- and stroke-related crucial modules, 24 common genes for T2DM-related stroke were identified. Metascape showed that neutrophil extracellular trap formation was primarily enriched. The hub gene was granulin precursor (GRN), which had the highest connectivity among the common genes. In addition, functional enrichment analysis indicated that GRN was involved in neutrophil degranulation, thus regulating neutrophil extracellular trap formation.\nCONCLUSIONS: This study firstly revealed that neutrophil extracellular trap formation may represent the common biological processes of diabetes and stroke, and GRN may be potential intervention targets for T2DM-related stroke.", "claims": [{"id": "claim-method", "statement": "The key modules for stroke and diabetes were identified by weight gene co-expression network analysis (WGCNA).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38166912", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "The key modules for stroke and diabetes were identified by weight gene co-expression network analysis (WGCNA)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All data from the GSE38642, GSE44035, GSE16561, and GSE22255 datasets are available at the GEO database (https://www.ncbi.nlm.nih.gov/geo/).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38166912", "locator": "sections[23] \"Availability of data and materials\" paragraph 2", "quote": "All data from the GSE38642, GSE44035, GSE16561, and GSE22255 datasets are available at the GEO database (https://www.ncbi.nlm.nih.gov/geo/)."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Intersecting the diabetes- and stroke-related crucial modules identified 24 common genes for T2DM-related stroke, with GRN identified as the hub gene.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:38166912", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "By intersecting the diabetes- and stroke-related crucial modules, 24 common genes for T2DM-related stroke were identified."}, {"asset": "source:pmid:38166912", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "The hub gene was granulin precursor (GRN), which had the highest connectivity among the common genes."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Intersecting the diabetes- and stroke-related crucial modules identified 24 common genes for T2DM-related stroke, with GRN identified as the hub gene.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:38166912"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE16561"], "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:GSE16561"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:38166912", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1186/s12920-023-01752-z", "sha256": 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