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pmid:37519764

Immune-dysregulated neutrophils characterized by upregulation of CXCL1 may be a potential factor in the pathogenesis of abdominal aortic aneurysm and systemic lupus erythematosus.

Lin Zhang · Que Li · Chenxing Zhou · Zhanman Zhang · Jiangfeng Zhang · Xiao Qin

Heliyon · 2023 doi:10.1016/j.heliyon.2023.e18037

Paper

complete

Experiment

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Data

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Analysis

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title
Immune-dysregulated neutrophils characterized by upregulation of CXCL1 may be a potential factor in the pathogenesis of abdominal aortic aneurysm and systemic lupus erythematosus.
doi
10.1016/j.heliyon.2023.e18037
pmid
37519764
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[0]
Lin Zhang
[1]
Que Li
[2]
Chenxing Zhou
[3]
Zhanman Zhang
[4]
Jiangfeng Zhang
[5]
Xiao Qin
journal
Heliyon
year
2023
abstract
Background: The abdominal aortic aneurysm (AAA) incidence is closely related to systemic lupus erythematosus (SLE). However, the common mechanisms between AAA and SLE are still unknown. The purpose of this research was to examine the main molecules and pathways involved in the immunization process that lead to the co-occurrence of AAA and SLE through the utilization of quantitative bioinformatics analysis of publicly available RNA sequencing databases. Moreover, routine blood test information was gathered from 460 patients to validate the findings. Materials and methods: Datasets of both AAA (GSE57691 and GSE205071) and SLE (GSE50772 and GSE154851) were downloaded from the Gene Expression Omnibus (GEO) database, and differentially expressed genes (DEGs) were analyzed using bioinformatic tools. To determine the functions of the common differentially expressed genes (DEGs), Gene Ontology (GO) and Kyoto Encyclopedia analyses were conducted. Subsequently, the hub gene was identified through cytoHubba, and its validation was carried out in GSE47472 for AAA and GSE81622 for SLE. Immune cell infiltration analysis was performed to identify the key immune cells correlated with AAA and SLE, and to evaluate the correlation between key immune cells and the hub gene. Subsequently, the routine blood test data of 460 patients were collected, and the result of the immune cell infiltration analysis was further validated by univariate and multivariate logistic regression analysis. Results: A total of 25 common DEGs were obtained, and three genes were screened by cytoHubba algorithms. Upon validation of the datasets, CXCL1 emerged as the hub gene with strong predictive capabilities, as evidenced by an area under the curve (AUC) > 0.7 for both AAA and SLE. The infiltration of immune cells was also validated, revealing a significant upregulation of neutrophils in the AAA and SLE datasets, along with a correlation between neutrophil infiltration and CXCL1 upregulation. Clinical data analysis revealed a significant increase in neutrophils in both AAA and SLE patients (p < 0.05). Neutrophils were found to be an independent factor in the diagnosis of AAA and SLE, exhibiting good diagnostic accuracy with AUC >0.7. Conclusion: This study elucidates CXCL1 as a hub gene for the co-occurrence of AAA and SLE. Neutrophil infiltration plays a central role in the development of AAA and SLE and may serve to be a potential diagnostic and therapeutic target.
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The data were normalized and differentially expressed genes (DEGs) were obtained by the ‘limma’ package in R software [14]. The R package ‘veen’ was used to obtain common DEGs [15].
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The data were normalized and differentially expressed genes (DEGs) were obtained by the ‘limma’ package in R software [14].
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The R package ‘veen’ was used to obtain common DEGs [15].
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The study identified 25 common differentially expressed genes with the same expression patterns in abdominal aortic aneurysm and systemic lupus erythematosus.
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Considering the intersection of the Venn diagrams (Fig. 2 C, D), we identified 25 common DEGs that exhibited the same expression patterns, comprising 14 common upregulated genes and 11 common downregulated genes.
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GSM2159878
[50]
GSM2159879
[51]
GSM2159880
[52]
GSM2159881
[53]
GSM2159882
[54]
GSM2159883
sample_count
55
group_sizes
null
group_sizes_basis
null
platform
10558
taxon
Homo sapiens
title
Whole genome transcription and DNA methylation analysis of peripheral blood mononuclear cells identified aberrant gene regulation pathways in systemic lupus erythematosus [expression]
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
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[1]
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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
asset:data:geo:GSE57691 licence not read
[10]
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[11]
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analysis object · 4 fields
state
partial
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[0] object · 10 fields
id
method-1
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differential_expression
specific
limma_voom
label
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normalise_counts
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The data were normalized and differentially expressed genes (DEGs) were obtained by the ‘limma’ package in R software [14]. The R package ‘veen’ was used to obtain common DEGs [15].
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group_comparison
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missing_operations array · 1 item
[0]
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parameters object · 1 field
p_value
icance level was set at p-value <0
data_shapes array · 1 item
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evidence object · 3 fields
score
0.8
band
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quote
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id
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group_comparison
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label
Group comparison
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missing_operations array · 1 item
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group_comparison_mann_whitney
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parameters object · 1 field
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two_or_more_groups_continuous
evidence object · 3 fields
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quote
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data_shapes array · 1 item
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evidence object · 3 fields
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id
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[0]
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parameters object · 0 fields
data_shapes array · 1 item
[0]
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evidence object · 3 fields
score
0.8
band
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quote
chi-square
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gaps array · 1 item
[0]
method.reader_differs_from_extractor
capability object · 3 fields
state
complete
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[0] object · 6 fields
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capability:computational_analysis
label
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candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
tier
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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
R1
capability_id
capability:computational_analysis
availability_state
owned
basis
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
R1
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accessions array · 6 items
[0]
GSE57691
[1]
GSE205071
[2]
GSE50772
[3]
GSE154851
[4]
GSE47472
[5]
GSE81622
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[0]
GSE57691
[1]
GSE205071
[2]
GSE50772
[3]
GSE154851
[4]
GSE47472
[5]
GSE81622
statements array · 1 item
[0]
Data included in article/supp. material/referenced in article.
basis
The paper names GSE57691, GSE205071, GSE50772, GSE154851, GSE47472, GSE81622 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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normalise_counts
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differential_expression_fit
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fdr_bh
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source:pmid:37519764
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data:geo:GSE154851
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run_analysis
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data_gaps array · 1 item
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data:geo:GSE154851
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partial
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extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T18:48:20Z
independence
single_reader
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method
reordered
availability
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usage object · 3 fields
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10694
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cached_tokens
264
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[0] object · 4 fields
id
extraction
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complete
reader
MiniMax-M3.1-Flash
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minimax
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review.independent_reader
[1]
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[2]
review.human_critique
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absent
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not_run
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null
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execution.not_run
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pmid:37519764
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paper
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pmid:37519764
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id
source:pmid:37519764
type
manuscript
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PMID 37519764 full text
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id
data:geo:GSE154851
type
dataset
label
GEO GSE154851
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[0] object · 4 fields
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activity-reading-sci-2026-11-01
type
classification
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pmid:37519764
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paper
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pmid:37519764
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id
source:pmid:37519764
type
manuscript
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PMID 37519764 full text
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id
data:geo:GSE154851
type
dataset
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GEO GSE154851
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agent:corpus-assay-engine
[1] object · 4 fields
id
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type
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used array · 1 item
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source:pmid:37519764
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agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE154851
type
accession_resolution
used array · 1 item
[0]
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agent:corpus-assay-engine
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agent:corpus-assay-engine
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software
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agent:minimax-reader
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sha256:68621b3885a822400564ad626ee886c20c6da9e9118bb5f2882c8144757055c6
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[9]
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[11]
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role
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differential_expression_fit
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dsl_catalogue
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evidence array · 1 item
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The data were normalized and differentially expressed genes (DEGs) were obtained by the ‘limma’ package in R software [14]. The R package ‘veen’ was used to obtain common DEGs [15].
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37519764", "kind": "science-record", "revision": 5, "content_hash": "sha256:bcb91d87955f02c898251ed98cdc28fd041d0e621c77681a5aa4f7117ed0e28b", "created_at": "2026-11-01T19:02:17Z", "updated_at": "2026-11-01T22:52:24Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Immune-dysregulated neutrophils characterized by upregulation of CXCL1 may be a potential factor in the pathogenesis of abdominal aortic aneurysm and systemic lupus erythematosus.", "doi": "10.1016/j.heliyon.2023.e18037", "pmid": "37519764", "authors": ["Lin Zhang", "Que Li", "Chenxing Zhou", "Zhanman Zhang", "Jiangfeng Zhang", "Xiao Qin"], "journal": "Heliyon", "year": 2023, "abstract": "Background: The abdominal aortic aneurysm (AAA) incidence is closely related to systemic lupus erythematosus (SLE). However, the common mechanisms between AAA and SLE are still unknown. The purpose of this research was to examine the main molecules and pathways involved in the immunization process that lead to the co-occurrence of AAA and SLE through the utilization of quantitative bioinformatics analysis of publicly available RNA sequencing databases. Moreover, routine blood test information was gathered from 460 patients to validate the findings.\nMaterials and methods: Datasets of both AAA (GSE57691 and GSE205071) and SLE (GSE50772 and GSE154851) were downloaded from the Gene Expression Omnibus (GEO) database, and differentially expressed genes (DEGs) were analyzed using bioinformatic tools. To determine the functions of the common differentially expressed genes (DEGs), Gene Ontology (GO) and Kyoto Encyclopedia analyses were conducted. Subsequently, the hub gene was identified through cytoHubba, and its validation was carried out in GSE47472 for AAA and GSE81622 for SLE. Immune cell infiltration analysis was performed to identify the key immune cells correlated with AAA and SLE, and to evaluate the correlation between key immune cells and the hub gene. Subsequently, the routine blood test data of 460 patients were collected, and the result of the immune cell infiltration analysis was further validated by univariate and multivariate logistic regression analysis.\nResults: A total of 25 common DEGs were obtained, and three genes were screened by cytoHubba algorithms. Upon validation of the datasets, CXCL1 emerged as the hub gene with strong predictive capabilities, as evidenced by an area under the curve (AUC) > 0.7 for both AAA and SLE. The infiltration of immune cells was also validated, revealing a significant upregulation of neutrophils in the AAA and SLE datasets, along with a correlation between neutrophil infiltration and CXCL1 upregulation. Clinical data analysis revealed a significant increase in neutrophils in both AAA and SLE patients (p < 0.05). Neutrophils were found to be an independent factor in the diagnosis of AAA and SLE, exhibiting good diagnostic accuracy with AUC >0.7.\nConclusion: This study elucidates CXCL1 as a hub gene for the co-occurrence of AAA and SLE. Neutrophil infiltration plays a central role in the development of AAA and SLE and may serve to be a potential diagnostic and therapeutic target.", "claims": [{"id": "claim-method", "statement": "The data were normalized and differentially expressed genes (DEGs) were obtained by the ‘limma’ package in R software [14]. The R package ‘veen’ was used to obtain common DEGs [15].", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37519764", "locator": "sections[5] \"Identification of differentially expressed genes\" paragraph 2", "quote": "The data were normalized and differentially expressed genes (DEGs) were obtained by the ‘limma’ package in R software [14]."}, {"asset": "source:pmid:37519764", "locator": "sections[5] \"Identification of differentially expressed genes\" paragraph 2", "quote": "The R package ‘veen’ was used to obtain common DEGs [15]."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Data included in article/supp. material/referenced in article.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37519764", "locator": "sections[23] \"Data availability statement\" paragraph 2", "quote": "Data included in article/supp. material/referenced in article."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The study identified 25 common differentially expressed genes with the same expression patterns in abdominal aortic aneurysm and systemic lupus erythematosus.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37519764", "locator": "sections[13] \"Identification of common DEGs\" paragraph 2", "quote": "Considering the intersection of the Venn diagrams (Fig. 2 C, D), we identified 25 common DEGs that exhibited the same expression patterns, comprising 14 common upregulated genes and 11 common downregulated genes."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The study identified 25 common differentially expressed genes with the same expression patterns in abdominal aortic aneurysm and systemic lupus erythematosus.", "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:37519764"], "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:GSE154851"], "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:GSE154851"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:37519764", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1016/j.heliyon.2023.e18037", "sha256": 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