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pmid:40636547

Identifying Diagnostic Biomarkers for Electroacupuncture Treatment of Rheumatoid Arthritis Using Bioinformatic Analysis and Machine Learning Algorithms.

Yijun Sun · Guoqi Dong · Hui Gao · Yong Yao · Huayuan Yang

Journal of pain research · 2025 doi:10.2147/JPR.S517733

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

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2026-11-01T20:30:44Z
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2026-11-01T22:56:48Z
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title
Identifying Diagnostic Biomarkers for Electroacupuncture Treatment of Rheumatoid Arthritis Using Bioinformatic Analysis and Machine Learning Algorithms.
doi
10.2147/JPR.S517733
pmid
40636547
authors array · 5 items
[0]
Yijun Sun
[1]
Guoqi Dong
[2]
Hui Gao
[3]
Yong Yao
[4]
Huayuan Yang
journal
Journal of pain research
year
2025
abstract
Purpose: Rheumatoid arthritis (RA) is a persistent inflammatory condition, and electroacupuncture (EA) has been demonstrated to effectively reduce the symptoms associated with RA. However, the molecular mechanisms underlying the effects of EA in RA remained poorly understood. This study aimed to identify potential diagnostic biomarkers for RA and elucidated the molecular targets of EA by using bioinformatics analysis and machine learning algorithms in peripheral blood samples. Methods: We obtained datasets from the Gene Expression Omnibus(GEO) database containing samples from RA patients (GSE15573) and from RA patients after EA treatment (GSE59526) for bioinformatics analysis. Diagnostic biomarkers were identified using three distinct machine learning algorithms (LASSO, Random Forest and SVM-REF). A rat model of RA was established using Complete Freund's Adjuvant (CFA), and quantitative real-time PCR was performed to confirm the differential expression of identified diagnostic biomarkers and assess the modulatory impact of EA on these genes. Results: Twenty-six genes were identified as differentially expressed following EA treatment. Three machine learning algorithms converged on ARHGAP17 and VEGFB as potential diagnostic biomarkers for RA, exhibiting robust diagnostic performance (AUC > 0.75) and consistent expression patterns across multiple RA cohorts (GSE17755, GSE205962 and GSE93272). Besides, EA treatment significantly increased the paw withdrawal threshold (PWT) and the peripheral blood expression of both ARHGAP17 and VEGFB in CFA rats. Conclusion: This study employed three machine learning algorithms to identify potential diagnostic biomarkers for the alleviation of RA by EA. The biomarkers demonstrated robust diagnostic performance across multiple validation datasets. Furthermore, animal experiments confirmed that EA exerted a favorable regulatory effect on these diagnostic biomarkers. The findings of this study provided novel therapeutic targets for the EA treatment of RA.
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Diagnostic biomarkers were identified using three distinct machine learning algorithms (LASSO, Random Forest and SVM-REF).
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Diagnostic biomarkers were identified using three distinct machine learning algorithms (LASSO, Random Forest and SVM-REF).
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The datasets analyzed for this study can be found in the GEO (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc = GSE15573, GSE59526, GSE17755, GSE205962, and GSE93272).
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sections[22] "Data Sharing Statement" paragraph 2
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The datasets analyzed for this study can be found in the GEO (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc = GSE15573, GSE59526, GSE17755, GSE205962, and GSE93272).
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Three machine learning algorithms converged on ARHGAP17 and VEGFB as potential diagnostic biomarkers for RA, exhibiting robust diagnostic performance (AUC > 0.75) and consistent expression patterns across multiple RA cohorts (GSE17755, GSE205962 and GSE93272).
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sections[0] "Abstract" paragraph 3
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Three machine learning algorithms converged on ARHGAP17 and VEGFB as potential diagnostic biomarkers for RA, exhibiting robust diagnostic performance (AUC > 0.75) and consistent expression patterns across multiple RA cohorts (GSE17755, GSE205962 and GSE93272).
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Three machine learning algorithms converged on ARHGAP17 and VEGFB as potential diagnostic biomarkers for RA, exhibiting robust diagnostic performance (AUC > 0.75) and consistent expression patterns across multiple RA cohorts (GSE17755, GSE205962 and GSE93272).
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Immunity and Defense Genes in Peripheral Blood Mononuclear Cells of Rheumatoid Arthritis patients
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access_statement_verbatim
The datasets analyzed for this study can be found in the GEO (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc = GSE15573, GSE59526, GSE17755, GSE205962, and GSE93272).
access_statement_kind
data_availability_statement
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sample_count
275
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Whole blood gene expression of rheumatoid arthritis
resolution_checked_at
2026-11-01T17:30:42Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
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gaps array · 10 items
[0]
asset:data:geo:GSE15573 not downloaded
[1]
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[2]
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[3]
asset:data:geo:GSE17755 licence not read
[4]
asset:data:geo:GSE205962 not downloaded
[5]
asset:data:geo:GSE205962 licence not read
[6]
asset:data:geo:GSE59526 not downloaded
[7]
asset:data:geo:GSE59526 licence not read
[8]
asset:data:geo:GSE93272 not downloaded
[9]
asset:data:geo:GSE93272 licence not read
analysis object · 4 fields
state
complete
methods array · 3 items
[0] object · 10 fields
id
method-1
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group_comparison
specific
anova
label
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dsl_operations array · 4 items
[0]
group_summary
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welch_t
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[3]
group_comparison_anova
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
two_or_more_groups_continuous
evidence object · 3 fields
score
1
band
verbatim
quote
Diagnostic biomarkers were identified using three distinct machine learning algorithms (LASSO, Random Forest and SVM-REF).
[1] object · 10 fields
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method-2
family
machine_learning
specific
random_forest
label
Machine learning
dsl_operations array · 0 items
missing_operations array · 1 item
[0]
machine_learning_random_forest
expressible
false
parameters object · 0 fields
data_shapes array · 1 item
[0]
labelled_feature_matrix
evidence object · 3 fields
score
0.7
band
medium
quote
Random Forest
[2] object · 10 fields
id
method-3
family
machine_learning
specific
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label
Machine learning
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[0]
train_classifier
[1]
cross_validate
[2]
roc_auc
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
labelled_feature_matrix
evidence object · 3 fields
score
0.7
band
medium
quote
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gaps array · 0 items
capability object · 3 fields
state
complete
requirements array · 1 item
[0] object · 6 fields
capability_id
capability:computational_analysis
label
Computational analysis platform
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[0]
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[7]
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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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blocked_on
nothing:replicable_now
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group_summary
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: anova.
capability object · 4 fields
tier
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capability:computational_analysis
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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
accessions array · 5 items
[0]
GSE15573
[1]
GSE59526
[2]
GSE17755
[3]
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[4]
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resolved_accessions array · 5 items
[0]
GSE15573
[1]
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[2]
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[3]
GSE205962
[4]
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statements array · 1 item
[0]
The datasets analyzed for this study can be found in the GEO (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc = GSE15573, GSE59526, GSE17755, GSE205962, and GSE93272).
basis
The paper names GSE15573, GSE59526, GSE17755, GSE205962, GSE93272 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
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group_summary
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bootstrap_mean_difference
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group_comparison_anova
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source:pmid:40636547
[1]
data:geo:GSE15573
steps array · 1 item
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run_analysis
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converters array · 0 items
readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE15573
gaps array · 0 items
review object · 5 fields
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partial
machine_critique object · 5 fields
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extraction_review
reader object · 5 fields
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MiniMax-M3.1-Flash
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minimax
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minimax
read_at
2026-11-01T19:56:56Z
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single_reader
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verbatim
availability
verbatim
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5
usage object · 3 fields
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8170
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3057
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256
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extraction
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complete
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pmid:40636547
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paper
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pmid:40636547
[1] object · 3 fields
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source:pmid:40636547
type
manuscript
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PMID 40636547 full text
[2] object · 3 fields
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data:geo:GSE15573
type
dataset
label
GEO GSE15573
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
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pmid:40636547
type
paper
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pmid:40636547
[1] object · 3 fields
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source:pmid:40636547
type
manuscript
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PMID 40636547 full text
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data:geo:GSE15573
type
dataset
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GEO GSE15573
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agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-40636547
type
extraction
used array · 1 item
[0]
source:pmid:40636547
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agent:minimax-reader
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activity-resolve-GSE15573
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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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lineage object · 4 fields
parent_id
pmid:40636547
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[1]
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[2]
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[3]
asset:data:geo:GSE17755 not downloaded
[4]
asset:data:geo:GSE205962 licence not read
[5]
asset:data:geo:GSE205962 not downloaded
[6]
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[7]
asset:data:geo:GSE59526 not downloaded
[8]
asset:data:geo:GSE93272 licence not read
[9]
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[10]
execution.not_run
[11]
review.human_critique
[12]
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[13]
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assays array · 3 items
[0] object · 11 fields
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data_generation
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animal_model
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99e1195c7d6f
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partial
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evidence array · 4 items
[0]
rithms (LASSO, Random Forest and SVM-REF). A rat model of RA was established using Complete F
[1]
expression of both ARHGAP17 and VEGFB in CFA rats. Conclusion: This study employed three machi
[2]
versity of Traditional Chinese Medicine. The rats were provided with free access to food and water
[3]
pathogen free (SPF) male Sprague-Dawley (SD) rats aged 8 weeks weighing 160–200 g were procure
order_basis
paper_text_order:919
id
assay:1
[1] object · 11 fields
role
data_generation
definition_version
99e1195c7d6f
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partial
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99e1195c7d6f
confidence
0.99
evidence array · 2 items
[0]
te Freund's Adjuvant (CFA), and quantitative real-time PCR was performed to confirm the differential ex
[1]
wed by Bonferroni post hoc tests applied for qPCR analysis, while behavioral analysis was cond
order_basis
paper_text_order:1008
id
assay:2
[2] object · 11 fields
role
analysis
definition_id
group_comparison
definition_version
f2132e96ae6c7a4e
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[0]
group_summary
[1]
welch_t
[2]
bootstrap_mean_difference
[3]
group_comparison_anova
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
Diagnostic biomarkers were identified using three distinct machine learning algorithms (LASSO, Random Forest and SVM-REF).
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consumes_earlier_output
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:40636547", "kind": "science-record", "revision": 4, "content_hash": "sha256:4a2a9a07665c139fd16bb830965f58fdcad9183984aca5b0dbf892fe86d79762", "created_at": "2026-11-01T20:30:44Z", "updated_at": "2026-11-01T22:56:48Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identifying Diagnostic Biomarkers for Electroacupuncture Treatment of Rheumatoid Arthritis Using Bioinformatic Analysis and Machine Learning Algorithms.", "doi": "10.2147/JPR.S517733", "pmid": "40636547", "authors": ["Yijun Sun", "Guoqi Dong", "Hui Gao", "Yong Yao", "Huayuan Yang"], "journal": "Journal of pain research", "year": 2025, "abstract": "Purpose: Rheumatoid arthritis (RA) is a persistent inflammatory condition, and electroacupuncture (EA) has been demonstrated to effectively reduce the symptoms associated with RA. However, the molecular mechanisms underlying the effects of EA in RA remained poorly understood. This study aimed to identify potential diagnostic biomarkers for RA and elucidated the molecular targets of EA by using bioinformatics analysis and machine learning algorithms in peripheral blood samples.\nMethods: We obtained datasets from the Gene Expression Omnibus(GEO) database containing samples from RA patients (GSE15573) and from RA patients after EA treatment (GSE59526) for bioinformatics analysis. Diagnostic biomarkers were identified using three distinct machine learning algorithms (LASSO, Random Forest and SVM-REF). A rat model of RA was established using Complete Freund's Adjuvant (CFA), and quantitative real-time PCR was performed to confirm the differential expression of identified diagnostic biomarkers and assess the modulatory impact of EA on these genes.\nResults: Twenty-six genes were identified as differentially expressed following EA treatment. Three machine learning algorithms converged on ARHGAP17 and VEGFB as potential diagnostic biomarkers for RA, exhibiting robust diagnostic performance (AUC > 0.75) and consistent expression patterns across multiple RA cohorts (GSE17755, GSE205962 and GSE93272). Besides, EA treatment significantly increased the paw withdrawal threshold (PWT) and the peripheral blood expression of both ARHGAP17 and VEGFB in CFA rats.\nConclusion: This study employed three machine learning algorithms to identify potential diagnostic biomarkers for the alleviation of RA by EA. The biomarkers demonstrated robust diagnostic performance across multiple validation datasets. Furthermore, animal experiments confirmed that EA exerted a favorable regulatory effect on these diagnostic biomarkers. 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A rat model of RA was established using Complete F", "expression of both ARHGAP17 and VEGFB in CFA rats. Conclusion: This study employed three machi", "versity of Traditional Chinese Medicine. The rats were provided with free access to food and water", "pathogen free (SPF) male Sprague-Dawley (SD) rats aged 8 weeks weighing 160–200 g were procure"], "order_basis": "paper_text_order:919", "id": "assay:1"}, {"role": "data_generation", "definition_id": "qpcr", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["te Freund's Adjuvant (CFA), and quantitative real-time PCR was performed to confirm the differential ex", "wed by Bonferroni post hoc tests applied for qPCR analysis, while behavioral analysis was cond"], "order_basis": "paper_text_order:1008", "id": "assay:2"}, {"role": "analysis", "definition_id": "group_comparison", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["group_summary", "welch_t", "bootstrap_mean_difference", "group_comparison_anova"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["Diagnostic biomarkers were identified using three distinct machine learning algorithms (LASSO, Random Forest and SVM-REF)."], "order_basis": "consumes_earlier_output", "id": "assay:3"}]}