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pmid:38660376

Transcriptomic analysis identifies the shared diagnostic biomarkers and immune relationship between Atherosclerosis and abdominal aortic aneurysm based on fatty acid metabolism gene set.

Xuefeng Gu · Zhongxian Yu · Tianwei Qian · Yiqi Jin · Guoxiong Xu · Jiang Li · Jianfeng Gu · Ming Li · Ke Tao

Frontiers in molecular biosciences · 2024 doi:10.3389/fmolb.2024.1365447

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Experiment

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Data

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pmid:38660376
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title
Transcriptomic analysis identifies the shared diagnostic biomarkers and immune relationship between Atherosclerosis and abdominal aortic aneurysm based on fatty acid metabolism gene set.
doi
10.3389/fmolb.2024.1365447
pmid
38660376
authors array · 9 items
[0]
Xuefeng Gu
[1]
Zhongxian Yu
[2]
Tianwei Qian
[3]
Yiqi Jin
[4]
Guoxiong Xu
[5]
Jiang Li
[6]
Jianfeng Gu
[7]
Ming Li
[8]
Ke Tao
journal
Frontiers in molecular biosciences
year
2024
abstract
Background: Epidemiological research has demonstrated that there is a connection between lipid metabolism disorder and an increased risk of developing arteriosclerosis (AS) and abdominal aortic aneurysm (AAA). However, the precise relationship between lipid metabolism, AS, and AAA is still not fully understood. The objective of this study was to examine the pathways and potential fatty acid metabolism-related genes (FRGs) that are shared between AS and AAA. Methods: AS- and AAA-associated datasets were retrieved from the Gene Expression Omnibus (GEO) database, and the limma package was utilized to identify differentially expressed FRGs (DFRGs) common to both AS and AAA patients. Functional enrichment analysis was conducted on the (DFRGs), and a protein-protein interaction (PPI) network was established. The selection of signature genes was performed through the utilization of least absolute shrinkage and selection operator (LASSO) regression and random forest (RF). Subsequently, a nomogram was developed using the results of the screening process, and the crucial genes were validated in two separate external datasets (GSE28829 and GSE17901) as well as clinical samples. In the end, single-sample gene set enrichment analysis (ssGSEA) was utilized to assess the immune cell patterns in both AS and AAA. Additionally, the correlation between key crosstalk genes and immune cell was evaluated. Results: In comparison to control group, both AS and AAA patients exhibited a decrease in fatty acid metabolism score. We found 40 DFRGs overlapping in AS and AAA, with lipid and amino acid metabolism critical in their pathogenesis. PCBD1, ACADL, MGLL, BCKDHB, and IDH3G were identified as signature genes connecting AS and AAA. Their expression levels were confirmed in validation datasets and clinical samples. The analysis of immune infiltration showed that neutrophils, NK CD56dim cells, and Tem cells are important in AS and AAA development. Correlation analysis suggested that these signature genes may be involved in immune cell infiltration. Conclusion: The fatty acid metabolism pathway appears to be linked to the development of both AS and AAA. Furthermore, PCBD1, ACADL, MGLL, BCKDHB, and IDH3G have the potential to serve as diagnostic markers for patients with AS complicated by AAA.
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We utilized the limma package to conduct a comparative analysis of gene expression between the control (Con) and disease groups.
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We utilized the limma package to conduct a comparative analysis of gene expression between the control (Con) and disease groups.
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All data used in the present study were available from the GEO database (https://www.ncbi.nlm.nih.gov/geo/).
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PCBD1, ACADL, MGLL, BCKDHB, and IDH3G were identified as signature genes connecting AS and AAA.
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PCBD1, ACADL, MGLL, BCKDHB, and IDH3G were identified as signature genes connecting AS and AAA.
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PCBD1, ACADL, MGLL, BCKDHB, and IDH3G were identified as signature genes connecting AS and AAA.
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GSM2590415
[46]
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[47]
GSM2590417
sample_count
48
group_sizes
null
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null
platform
10558
taxon
Homo sapiens
title
A molecular fingerprint for terminal abdominal aortic aneurysm progression
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
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[3]
asset:data:geo:GSE17901 licence not read
[4]
asset:data:geo:GSE28829 not downloaded
[5]
asset:data:geo:GSE28829 licence not read
[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
complete
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id
method-1
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differential_expression
specific
limma_voom
label
Differential expression analysis
dsl_operations array · 3 items
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normalise_counts
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differential_expression_fit
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fdr_bh
missing_operations array · 0 items
parameters object · 0 fields
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evidence object · 3 fields
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1
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quote
We utilized the limma package to conduct a comparative analysis of gene expression between the control (Con) and disease groups.
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id
method-2
family
machine_learning
specific
random_forest
label
Machine learning
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missing_operations array · 1 item
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machine_learning_random_forest
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parameters object · 0 fields
data_shapes array · 1 item
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labelled_feature_matrix
evidence object · 3 fields
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0.7
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id
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ppi_network
label
Network / pathway analysis
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[1]
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data_shapes array · 1 item
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evidence object · 3 fields
score
0.7
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quote
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id
method-4
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label
Network / pathway analysis
dsl_operations array · 1 item
[0]
pathway_enrich
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
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evidence object · 3 fields
score
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band
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quote
GO enrichment
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gaps array · 0 items
capability object · 3 fields
state
complete
requirements array · 1 item
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capability_id
capability:computational_analysis
label
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assay_families array · 9 items
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[1]
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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
state
complete
tier
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tier
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fdr_bh
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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
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accessions array · 6 items
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[1]
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[2]
GSE98278
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GSE17901
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GSE100927
[5]
GSE28829
resolved_accessions array · 6 items
[0]
GSE57691
[1]
GSE47472
[2]
GSE98278
[3]
GSE17901
[4]
GSE100927
[5]
GSE28829
statements array · 1 item
[0]
All data used in the present study were available from the GEO database (https://www.ncbi.nlm.nih.gov/geo/).
basis
The paper names GSE57691, GSE47472, GSE98278, GSE17901, GSE100927, GSE28829 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 3 items
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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:38660376
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data:geo:GSE100927
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run_analysis
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data:geo:GSE100927
gaps array · 0 items
review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
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model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T19:16:57Z
independence
single_reader
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method
verbatim
availability
verbatim
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9911
completion_tokens
2529
cached_tokens
264
stages array · 1 item
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id
extraction
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complete
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MiniMax-M3.1-Flash
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minimax
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not_run
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gaps array · 1 item
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entities array · 3 items
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id
pmid:38660376
type
paper
label
pmid:38660376
[1] object · 3 fields
id
source:pmid:38660376
type
manuscript
label
PMID 38660376 full text
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id
data:geo:GSE100927
type
dataset
label
GEO GSE100927
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[0] object · 4 fields
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activity-reading-sci-2026-11-01
type
classification
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id
pmid:38660376
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paper
label
pmid:38660376
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id
source:pmid:38660376
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manuscript
label
PMID 38660376 full text
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id
data:geo:GSE100927
type
dataset
label
GEO GSE100927
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agent:corpus-assay-engine
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activity-read-38660376
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source:pmid:38660376
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agent:minimax-reader
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activity-resolve-GSE100927
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data:geo:GSE100927
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agent:corpus-assay-engine
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agent:corpus-assay-engine
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dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
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lineage object · 4 fields
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pmid:38660376
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sha256:027b2675c78d0b4aff99a5e343b044456aa60c06e6722b4ee9cc0f7047321027
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[0]
T-PCR) analysis was performed using the SYBR qPCR Master Mix (Bio-Rad) after reverse transcrip
[1]
s provided by the manufacturer. Quantitative real-time PCR (qRT-PCR) analysis was performed using the S
[2]
Thermo Fisher). We utilized the Roche LC480 Real-Time PCR System to quantify the expression levels of
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paper_text_order:3426
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assay:1
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We utilized the limma package to conduct a comparative analysis of gene expression between the control (Con) and disease groups.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38660376", "kind": "science-record", "revision": 4, "content_hash": "sha256:998f891deb823ae59e947a8ed169e35b12335a10dc62be7e108aeb21a5b1eb27", "created_at": "2026-11-01T19:20:38Z", "updated_at": "2026-11-01T22:54:12Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Transcriptomic analysis identifies the shared diagnostic biomarkers and immune relationship between Atherosclerosis and abdominal aortic aneurysm based on fatty acid metabolism gene set.", "doi": "10.3389/fmolb.2024.1365447", "pmid": "38660376", "authors": ["Xuefeng Gu", "Zhongxian Yu", "Tianwei Qian", "Yiqi Jin", "Guoxiong Xu", "Jiang Li", "Jianfeng Gu", "Ming Li", "Ke Tao"], "journal": "Frontiers in molecular biosciences", "year": 2024, "abstract": "Background: Epidemiological research has demonstrated that there is a connection between lipid metabolism disorder and an increased risk of developing arteriosclerosis (AS) and abdominal aortic aneurysm (AAA). However, the precise relationship between lipid metabolism, AS, and AAA is still not fully understood. The objective of this study was to examine the pathways and potential fatty acid metabolism-related genes (FRGs) that are shared between AS and AAA.\nMethods: AS- and AAA-associated datasets were retrieved from the Gene Expression Omnibus (GEO) database, and the limma package was utilized to identify differentially expressed FRGs (DFRGs) common to both AS and AAA patients. Functional enrichment analysis was conducted on the (DFRGs), and a protein-protein interaction (PPI) network was established. The selection of signature genes was performed through the utilization of least absolute shrinkage and selection operator (LASSO) regression and random forest (RF). Subsequently, a nomogram was developed using the results of the screening process, and the crucial genes were validated in two separate external datasets (GSE28829 and GSE17901) as well as clinical samples. In the end, single-sample gene set enrichment analysis (ssGSEA) was utilized to assess the immune cell patterns in both AS and AAA. Additionally, the correlation between key crosstalk genes and immune cell was evaluated.\nResults: In comparison to control group, both AS and AAA patients exhibited a decrease in fatty acid metabolism score. We found 40 DFRGs overlapping in AS and AAA, with lipid and amino acid metabolism critical in their pathogenesis. PCBD1, ACADL, MGLL, BCKDHB, and IDH3G were identified as signature genes connecting AS and AAA. Their expression levels were confirmed in validation datasets and clinical samples. The analysis of immune infiltration showed that neutrophils, NK CD56dim cells, and Tem cells are important in AS and AAA development. Correlation analysis suggested that these signature genes may be involved in immune cell infiltration.\nConclusion: The fatty acid metabolism pathway appears to be linked to the development of both AS and AAA. Furthermore, PCBD1, ACADL, MGLL, BCKDHB, and IDH3G have the potential to serve as diagnostic markers for patients with AS complicated by AAA.", "claims": [{"id": "claim-method", "statement": "We utilized the limma package to conduct a comparative analysis of gene expression between the control (Con) and disease groups.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38660376", "locator": "sections[4] \"Identifying differentially expressed genes (DEGs)\" paragraph 2", "quote": "We utilized the limma package to conduct a comparative analysis of gene expression between the control (Con) and disease groups."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All data used in the present study were available from the GEO database (https://www.ncbi.nlm.nih.gov/geo/).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38660376", "locator": "sections[21] \"Data availability statement\" paragraph 2", "quote": "All data used in the present study were available from the GEO database (https://www.ncbi.nlm.nih.gov/geo/)."}], "state": "complete"}, {"id": "claim-target-result", "statement": "PCBD1, ACADL, MGLL, BCKDHB, and IDH3G were identified as signature genes connecting AS and AAA.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:38660376", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "PCBD1, ACADL, MGLL, BCKDHB, and IDH3G were identified as signature genes connecting AS and AAA."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "PCBD1, ACADL, MGLL, BCKDHB, and IDH3G were identified as signature genes connecting AS and AAA.", "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:38660376"], "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:GSE100927"], "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:GSE100927"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:38660376", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fmolb.2024.1365447", "sha256": 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