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pmid:41461688

Deciphering the clinical implication of an obesity-related gene signature as the novel biomarker for acute myocardial infarction diagnosis.

Weixia Dong · Zixin Xue · Min Zhang · Feng Lu · Shaoping Ji

Scientific reports · 2025 doi:10.1038/s41598-025-28461-0

Paper

complete

Experiment

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Data

partial

Analysis

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title
Deciphering the clinical implication of an obesity-related gene signature as the novel biomarker for acute myocardial infarction diagnosis.
doi
10.1038/s41598-025-28461-0
pmid
41461688
authors array · 5 items
[0]
Weixia Dong
[1]
Zixin Xue
[2]
Min Zhang
[3]
Feng Lu
[4]
Shaoping Ji
journal
Scientific reports
year
2025
abstract
Acute myocardial infarction (AMI) stands as a major contributor to mortality and disability worldwide, with obesity playing a significant role in its development. This study aims to investigate potential biomarkers associated with obesity-related genes (ORGs) in patients with AMI. We downloaded four training gene expression datasets and one validation dataset from the Gene Expression Omnibus (GEO) database, and extracted ORGs from the GeneCards database. Feature genes were identified using machine learning techniques, and their diagnostic potential was evaluated through receiver operating characteristic (ROC) curves. To assess the identified critical pathways, Gene Set Enrichment Analysis (GSEA) was performed. Levels of immune infiltration were analyzed using the CIBERSORT algorithm and single-sample Gene Set Enrichment Analysis (ssGSEA). A signature comprising five genes (IL1RN, TLR2, NFKBIA, MMP9, and ITLN1) was established as a diagnostic biomarker for AMI, achieving an area under the curve (AUC) of 0.924, which was confirmed in the GSE59876 dataset (AUC = 0.825). According to the diagnostic model, comparisons between high- and low-risk groups revealed six distinct immune cell types and thirteen differing immune functions. Validation through reverse transcription quantitative polymerase chain reaction (RT-qPCR) reaffirmed the differential expression of the signature genes in AMI and control samples. Our findings provide crucial insights into the roles of ORGs in AMI and may facilitate the identification of valuable biomarkers for AMI diagnosis.
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The “limma” package in R was applied for background correction, inter-array normalization, and analysis of differential expression between AMI and control samples.
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The “limma” package in R was applied for background correction, inter-array normalization, and analysis of differential expression between AMI and control samples.
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All data generated or analyzed during this study are included in this published article. The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
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A signature comprising five genes (IL1RN, TLR2, NFKBIA, MMP9, and ITLN1) was established as a diagnostic biomarker for AMI, achieving an area under the curve (AUC) of 0.924, which was confirmed in the GSE59876 dataset (AUC = 0.825).
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A signature comprising five genes (IL1RN, TLR2, NFKBIA, MMP9, and ITLN1) was established as a diagnostic biomarker for AMI, achieving an area under the curve (AUC) of 0.924, which was confirmed in the GSE59876 dataset (AUC = 0.825).
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A signature comprising five genes (IL1RN, TLR2, NFKBIA, MMP9, and ITLN1) was established as a diagnostic biomarker for AMI, achieving an area under the curve (AUC) of 0.924, which was confirmed in the GSE59876 dataset (AUC = 0.825).
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A signature comprising five genes (IL1RN, TLR2, NFKBIA, MMP9, and ITLN1) was established as a diagnostic biomarker for AMI, achieving an area under the curve (AUC) of 0.924, which was confirmed in the GSE59876 dataset (AUC = 0.825).
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GSM1448724
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GSM1620759
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GSM1620760
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[394]
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[400]
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[402]
GSM1620771
[403]
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[404]
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[405]
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[406]
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[407]
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[410]
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[411]
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[423]
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[424]
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[425]
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[426]
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[428]
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[429]
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[430]
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[431]
GSM1620800
[432]
GSM1620801
[433]
GSM1620802
[434]
GSM1620803
[435]
GSM1620804
sample_count
436
group_sizes
null
group_sizes_basis
null
platform
6244
taxon
Homo sapiens
title
Gene expression profiling reveals potential prognostic biomarkers associated with the progression of heart failure
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[3] object · 15 fields
id
data:geo:GSE59876
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=GSE59876
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE59876
version
null
note
All data generated or analyzed during this study are included in this published article. The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
All data generated or analyzed during this study are included in this published article. The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
access_statement_kind
data_availability_statement
sample_accessions array · 7 items
[0]
GSM1448868
[1]
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[2]
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[3]
GSM1448871
[4]
GSM1448888
[5]
GSM1448889
[6]
GSM1448890
sample_count
7
group_sizes
null
group_sizes_basis
null
platform
19010;84
taxon
Pseudomonas aeruginosa PAO1; Pseudomonas aeruginosa
title
Pseudomonas aeruginosa LysR PA4203 regulator acts as a repressor of the PA4202 gene encoding a nitronate monooxygenase
resolution_checked_at
2026-11-01T20:16:08Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[4] object · 15 fields
id
data:geo:GSE60993
role
raw
format
geo-series
media_type
application/vnd.ncbi.geo-series+json
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE60993
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE60993
version
null
note
All data generated or analyzed during this study are included in this published article. The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
All data generated or analyzed during this study are included in this published article. The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
access_statement_kind
data_availability_statement
sample_accessions array · 33 items
[0]
GSM1495313
[1]
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[3]
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[4]
GSM1495317
[5]
GSM1495318
[6]
GSM1495319
[7]
GSM1495320
[8]
GSM1495321
[9]
GSM1495322
[10]
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[11]
GSM1495324
[12]
GSM1495325
[13]
GSM1495326
[14]
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[15]
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[16]
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[17]
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[18]
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[19]
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[20]
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[21]
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[22]
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[23]
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[24]
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[25]
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[26]
GSM1495339
[27]
GSM1495340
[28]
GSM1495341
[29]
GSM1495342
[30]
GSM1495343
[31]
GSM1495344
[32]
GSM1495345
sample_count
33
group_sizes
null
group_sizes_basis
null
platform
6884
taxon
Homo sapiens
title
Assessment and Diagnostic Relevance of Novel Serum Biomarkers for Early Decision of ST-elevation Myocardial Infarction
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[5] object · 15 fields
id
data:geo:GSE66360
role
raw
format
geo-series
media_type
application/vnd.ncbi.geo-series+json
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE66360
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE66360
version
null
note
All data generated or analyzed during this study are included in this published article. The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
All data generated or analyzed during this study are included in this published article. The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
access_statement_kind
data_availability_statement
sample_accessions array · 99 items
[0]
GSM1620819
[1]
GSM1620820
[2]
GSM1620821
[3]
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[4]
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[5]
GSM1620824
[6]
GSM1620825
[7]
GSM1620826
[8]
GSM1620827
[9]
GSM1620828
[10]
GSM1620829
[11]
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[12]
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[13]
GSM1620832
[14]
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[20]
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[24]
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[25]
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[26]
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[27]
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[28]
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[30]
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[37]
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[38]
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[39]
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[43]
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[69]
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[94]
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[95]
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[97]
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[98]
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sample_count
99
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
A Whole Blood Molecular Signature for the Identification of Acute Myocardial Infarction Without Relying Upon Myonecrosis (microarray)
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[6] object · 15 fields
id
data:geo:GSE97320
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raw
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geo-series
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application/vnd.ncbi.geo-series+json
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE97320
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null
bytes
null
access
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resolved
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null
reader_status
reader_required
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GSE97320
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null
note
All data generated or analyzed during this study are included in this published article. The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
structure object · 15 fields
repository
GEO
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GEO accession URL
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All data generated or analyzed during this study are included in this published article. The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
access_statement_kind
data_availability_statement
sample_accessions array · 6 items
[0]
GSM2561549
[1]
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[2]
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[3]
GSM2561552
[4]
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[5]
GSM2561554
sample_count
6
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null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Differential gene expression profiles in peripheral blood in Northeast Chinese Han people with acute myocardial infarction
resolution_checked_at
2026-11-01T18:06:44Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
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false
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[0]
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[1]
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[3]
asset:data:geo:GSE59867 licence not read
[4]
asset:data:geo:GSE59876 not downloaded
[5]
asset:data:geo:GSE59876 licence not read
[6]
asset:data:geo:GSE60993 not downloaded
[7]
asset:data:geo:GSE60993 licence not read
[8]
asset:data:geo:GSE66360 not downloaded
[9]
asset:data:geo:GSE66360 licence not read
[10]
asset:data:geo:GSE97320 not downloaded
[11]
asset:data:geo:GSE97320 licence not read
analysis object · 4 fields
state
complete
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[0] object · 10 fields
id
method-1
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differential_expression
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limma_voom
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Differential expression analysis
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[0]
normalise_counts
[1]
differential_expression_fit
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fdr_bh
missing_operations array · 0 items
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[0]
count_matrix_with_condition
evidence object · 3 fields
score
1
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verbatim
quote
The “limma” package in R was applied for background correction, inter-array normalization, and analysis of differential expression between AMI and control samples.
[1] object · 10 fields
id
method-2
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diagnostic_evaluation
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Diagnostic test evaluation
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[0]
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[0]
reference_standard_and_test
evidence object · 3 fields
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0.8
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high
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ROC curve
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[0] object · 8 fields
id
target-published-estimate
claim_id
claim-target-result
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classification_metrics
unit
auc
tolerance
null
state
complete
note
The published estimate as the reader quoted it from the paper. No tolerance is published because the paper states none.
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capability object · 3 fields
state
complete
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[0] object · 6 fields
capability_id
capability:computational_analysis
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Computational analysis platform
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[0]
meta_analysis
[1]
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[5]
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[6]
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[7]
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[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
gaps array · 0 items
readiness object · 8 fields
state
complete
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R1
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nothing:replicable_now
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method object · 5 fields
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R1
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[1]
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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
R1
reachable
true
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[0]
GSE48060
[1]
GSE60993
[2]
GSE66360
[3]
GSE97320
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GSE59867
[5]
GSE59876
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[0]
GSE48060
[1]
GSE60993
[2]
GSE66360
[3]
GSE97320
[4]
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[5]
GSE59876
statements array · 1 item
[0]
All data generated or analyzed during this study are included in this published article. The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
basis
The paper names GSE48060, GSE60993, GSE66360, GSE97320, GSE59867, GSE59876 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
[0]
normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
assets array · 2 items
[0]
source:pmid:41461688
[1]
data:geo:GSE48060
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run_analysis
must_build object · 5 fields
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readers array · 0 items
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[0]
data:geo:GSE48060
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review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T20:09:06Z
independence
single_reader
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method
verbatim
availability
verbatim
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5
usage object · 3 fields
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13060
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2138
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128
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[0] object · 4 fields
id
extraction
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complete
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MiniMax-M3.1-Flash
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minimax
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execution.not_run
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pmid:41461688
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paper
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pmid:41461688
[1] object · 3 fields
id
source:pmid:41461688
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manuscript
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PMID 41461688 full text
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id
data:geo:GSE48060
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dataset
label
GEO GSE48060
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[0] object · 4 fields
id
activity-reading-sci-2026-11-01
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classification
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id
pmid:41461688
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paper
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pmid:41461688
[1] object · 3 fields
id
source:pmid:41461688
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manuscript
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PMID 41461688 full text
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id
data:geo:GSE48060
type
dataset
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GEO GSE48060
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agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-41461688
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extraction
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[0]
source:pmid:41461688
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agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE48060
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accession_resolution
used array · 1 item
[0]
data:geo:GSE48060
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agent:corpus-assay-engine
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[0] object · 3 fields
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agent:corpus-assay-engine
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agent:minimax-reader
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343fb30756ba6ec3
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2cb3e42f047d2ecf
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pmid:41461688
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sha256:d3b75d42fba29e3d94c8764a58d48bd5a583eb23553cef3d92a5c594ad308046
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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:GSE66360 not downloaded
[10]
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[11]
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[13]
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[0] object · 11 fields
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data_generation
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99e1195c7d6f
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partial
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99e1195c7d6f
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0.99
evidence array · 2 items
[0]
tion quantitative polymerase chain reaction (RT-qPCR) reaffirmed the differential expression of t
[1]
n quantitative polymerase chain reaction (RT-qPCR) reaffirmed the differential expression of t
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paper_text_order:1422
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assay:1
[1] object · 11 fields
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analysis
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differential_expression
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f2132e96ae6c7a4e
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f2132e96ae6c7a4e
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[0]
The “limma” package in R was applied for background correction, inter-array normalization, and analysis of differential expression between AMI and control samples.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:41461688", "kind": "science-record", "revision": 4, "content_hash": "sha256:08137bd563de74851199da8b43d77c63d914abc2f8acbe8168937868d28bf439", "created_at": "2026-11-01T20:31:26Z", "updated_at": "2026-11-01T22:57:40Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Deciphering the clinical implication of an obesity-related gene signature as the novel biomarker for acute myocardial infarction diagnosis.", "doi": "10.1038/s41598-025-28461-0", "pmid": "41461688", "authors": ["Weixia Dong", "Zixin Xue", "Min Zhang", "Feng Lu", "Shaoping Ji"], "journal": "Scientific reports", "year": 2025, "abstract": "Acute myocardial infarction (AMI) stands as a major contributor to mortality and disability worldwide, with obesity playing a significant role in its development. This study aims to investigate potential biomarkers associated with obesity-related genes (ORGs) in patients with AMI. We downloaded four training gene expression datasets and one validation dataset from the Gene Expression Omnibus (GEO) database, and extracted ORGs from the GeneCards database. Feature genes were identified using machine learning techniques, and their diagnostic potential was evaluated through receiver operating characteristic (ROC) curves. To assess the identified critical pathways, Gene Set Enrichment Analysis (GSEA) was performed. Levels of immune infiltration were analyzed using the CIBERSORT algorithm and single-sample Gene Set Enrichment Analysis (ssGSEA). A signature comprising five genes (IL1RN, TLR2, NFKBIA, MMP9, and ITLN1) was established as a diagnostic biomarker for AMI, achieving an area under the curve (AUC) of 0.924, which was confirmed in the GSE59876 dataset (AUC = 0.825). According to the diagnostic model, comparisons between high- and low-risk groups revealed six distinct immune cell types and thirteen differing immune functions. Validation through reverse transcription quantitative polymerase chain reaction (RT-qPCR) reaffirmed the differential expression of the signature genes in AMI and control samples. Our findings provide crucial insights into the roles of ORGs in AMI and may facilitate the identification of valuable biomarkers for AMI diagnosis.", "claims": [{"id": "claim-method", "statement": "The “limma” package in R was applied for background correction, inter-array normalization, and analysis of differential expression between AMI and control samples.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41461688", "locator": "sections[3] \"Data acquisition, processing and identification of differentially expressed genes\" paragraph 2", "quote": "The “limma” package in R was applied for background correction, inter-array normalization, and analysis of differential expression between AMI and control samples."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All data generated or analyzed during this study are included in this published article. The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41461688", "locator": "sections[22] \"Data availability\" paragraph 2", "quote": "All data generated or analyzed during this study are included in this published article. The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request."}], "state": "complete"}, {"id": "claim-target-result", "statement": "A signature comprising five genes (IL1RN, TLR2, NFKBIA, MMP9, and ITLN1) was established as a diagnostic biomarker for AMI, achieving an area under the curve (AUC) of 0.924, which was confirmed in the GSE59876 dataset (AUC = 0.825).", "kind": "quantitative", "target": {"value": 0.825, "unit": "auc", "tolerance": null, "source": "A signature comprising five genes (IL1RN, TLR2, NFKBIA, MMP9, and ITLN1) was established as a diagnostic biomarker for AMI, achieving an area under the curve (AUC) of 0.924, which was confirmed in the GSE59876 dataset (AUC = 0.825)."}, "evidence": [{"asset": "source:pmid:41461688", "locator": "sections[0] \"Abstract\" paragraph 1", "quote": "A signature comprising five genes (IL1RN, TLR2, NFKBIA, MMP9, and ITLN1) was established as a diagnostic biomarker for AMI, achieving an area under the curve (AUC) of 0.924, which was confirmed in the GSE59876 dataset (AUC = 0.825)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "A signature comprising five genes (IL1RN, TLR2, NFKBIA, MMP9, and ITLN1) was established as a diagnostic biomarker for AMI, achieving an area under the curve (AUC) of 0.924, which was confirmed in the GSE59876 dataset (AUC = 0.825).", "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:41461688"], "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. 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