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pmid:40842654

Bioinformatics and experimental validation identify biomarkers for diagnosing Alzheimer's disease.

Hui Liu · Chenye Li · Congchen Zhai · Mei Li · Lan Ma

Frontiers in aging neuroscience · 2025 doi:10.3389/fnagi.2025.1566929

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
Bioinformatics and experimental validation identify biomarkers for diagnosing Alzheimer's disease.
doi
10.3389/fnagi.2025.1566929
pmid
40842654
authors array · 5 items
[0]
Hui Liu
[1]
Chenye Li
[2]
Congchen Zhai
[3]
Mei Li
[4]
Lan Ma
journal
Frontiers in aging neuroscience
year
2025
abstract
Background and purpose: Alzheimer's disease (AD) is a complex condition involving multiple mechanisms, primarily characterized by the progressive decline in cognition and memory. At present, there is no simple and reliable diagnostic method available for clinical application. Therefore, this study aims to identify potential biomarkers for AD using bioinformatics, providing new insights into its diagnosis. Methods: This study utilized the transcriptome dataset GSE63060 from the Gene Expression Omnibus (GEO) and applied bioinformatics approaches to identify candidate genes. Differentially expressed genes (DEGs), weighted gene co-expression network analysis (WGCNA), protein-protein interaction (PPI) networks, and machine learning techniques (LASSO, SVM-RFE, Boruta, and XGBoost) were employed on the GSE63060 dataset. Subsequently, the expression levels of the candidate genes were evaluated, and a receiver operating characteristic (ROC) curve was constructed to identify hub genes and establish a corresponding network. Finally, we focused on the common upstream transcription factor c-Myc among the hub genes and conducted clinical experiments to validate its potential. Serum samples were collected from 41 AD patients treated at the Second Affiliated Hospital of Harbin Medical University between October 2023 and November 2024, along with 41 control subjects. The c-Myc protein concentration was measured using ELISA, and a ROC curve was constructed to assess its diagnostic potential. Results: This study identified four hub genes associated with AD: RPL36AL, NDUFA1, NDUFS5, and RPS25. Additionally, the concentration of the c-Myc protein was significantly different between the AD and control groups (p < 0.001). The diagnostic sensitivity was 87.8%, specificity was 51.2%, and the area under the curve (AUC) value was 0.753, suggesting that c-Myc has independent diagnostic significance for AD. Conclusion: Our study demonstrates that RPL36AL, NDUFA1, NDUFS5, and RPS25 have potential as biomarkers for the diagnosis of AD. Additionally, the experiment suggests that c-Myc could serve as a promising blood biomarker for the diagnosis of AD.
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Pearson correlation analysis was performed on serum c-Myc levels, and the diagnostic value of serum c-Myc for AD was assessed using the ROC curve.
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Pearson correlation analysis was performed on serum c-Myc levels, and the diagnostic value of serum c-Myc for AD was assessed using the ROC curve.
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sections[38] "Data availability statement" paragraph 2
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The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.
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Serum c-Myc showed diagnostic significance for Alzheimer’s disease, with 87.8% sensitivity, 51.2% specificity, and an AUC of 0.753.
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GSM1539796
sample_count
388
group_sizes
null
group_sizes_basis
null
platform
10558
taxon
Homo sapiens
title
Alzheimer, Mild Cognitive impairment and control samples from AddneuroMed Cohort (batch 2)
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
gaps array · 4 items
[0]
asset:data:geo:GSE63060 not downloaded
[1]
asset:data:geo:GSE63060 licence not read
[2]
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[3]
asset:data:geo:GSE63061 licence not read
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[0] object · 10 fields
id
method-1
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machine_learning
specific
support_vector_machine
label
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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
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medium
quote
SVM
[1] object · 10 fields
id
method-2
family
machine_learning
specific
gradient_boosting
label
Machine learning
dsl_operations array · 3 items
[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
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quote
XGBoost
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id
method-3
family
correlation_analysis
specific
pearson
label
Correlation analysis
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[0]
pearson_r
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
paired_numeric_columns
evidence object · 3 fields
score
0.8
band
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quote
Pearson correlation
[3] object · 10 fields
id
method-4
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network_analysis
specific
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label
Network / pathway analysis
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[0]
build_graph
[1]
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[2]
pathway_enrich
missing_operations array · 0 items
parameters object · 0 fields
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[0]
edge_list
evidence object · 3 fields
score
0.7
band
medium
quote
protein-protein interaction
[4] object · 10 fields
id
method-5
family
diagnostic_evaluation
specific
roc
label
Diagnostic test evaluation
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[0]
confusion_counts
[1]
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[2]
sensitivity_specificity
[3]
solve_confusion_matrix
[4]
classification_metrics
[5]
published_precision_envelope
missing_operations array · 0 items
parameters object · 0 fields
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[0]
reference_standard_and_test
evidence object · 3 fields
score
0.7
band
medium
quote
ROC curve
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id
method-6
family
contingency_analysis
specific
chi_square
label
Categorical (contingency table) analysis
dsl_operations array · 1 item
[0]
chi_square_test
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
categorical_cross_tabulation
evidence object · 3 fields
score
0.8
band
high
quote
chi-square
[6] object · 10 fields
id
method-7
family
null
specific
null
label
Receiver operating characteristic (ROC) curve analysis
dsl_operations array · 0 items
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 0 items
evidence object · 3 fields
score
1
band
verbatim
quote
Pearson correlation analysis was performed on serum c-Myc levels, and the diagnostic value of serum c-Myc for AD was assessed using the ROC curve.
targets array · 1 item
[0] object · 8 fields
id
target-published-estimate
claim_id
claim-target-result
operation
build_graph
unit
p-value
tolerance
null
state
complete
note
The threshold the paper applied to its own result, as the paper states it. A run that reproduces the effect is judged against this threshold.
gaps array · 1 item
[0]
method.reader_named_unmapped
capability object · 3 fields
state
complete
requirements array · 1 item
[0] object · 6 fields
capability_id
capability:computational_analysis
label
Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
machine_learning
[2]
survival_analysis
[3]
statistical_regression
[4]
pca
[5]
molecular_docking
[6]
network_analysis
[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
tier
R1
blocked_on
nothing:replicable_now
axes object · 3 fields
method object · 5 fields
tier
R1
expressible
true
required_operations array · 3 items
[0]
train_classifier
[1]
cross_validate
[2]
roc_auc
missing_operations array · 0 items
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: support_vector_machine.
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
accessions array · 2 items
[0]
GSE63060
[1]
GSE63061
resolved_accessions array · 2 items
[0]
GSE63060
[1]
GSE63061
statements array · 1 item
[0]
The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.
basis
The paper names GSE63060, GSE63061 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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[0]
train_classifier
[1]
cross_validate
[2]
roc_auc
assets array · 2 items
[0]
source:pmid:40842654
[1]
data:geo:GSE63060
steps array · 1 item
[0]
run_analysis
must_build object · 5 fields
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readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE63060
gaps array · 0 items
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
2026-11-01T20:00:01Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
5
usage object · 3 fields
prompt_tokens
10940
completion_tokens
1499
cached_tokens
256
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[0] object · 4 fields
id
extraction
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complete
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MiniMax-M3.1-Flash
provider
minimax
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[0]
review.independent_reader
[1]
review.machine_critique
[2]
review.human_critique
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absent
status
not_run
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null
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gaps array · 1 item
[0]
execution.not_run
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[0] object · 3 fields
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pmid:40842654
type
paper
label
pmid:40842654
[1] object · 3 fields
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source:pmid:40842654
type
manuscript
label
PMID 40842654 full text
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data:geo:GSE63060
type
dataset
label
GEO GSE63060
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[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
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[0] object · 3 fields
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pmid:40842654
type
paper
label
pmid:40842654
[1] object · 3 fields
id
source:pmid:40842654
type
manuscript
label
PMID 40842654 full text
[2] object · 3 fields
id
data:geo:GSE63060
type
dataset
label
GEO GSE63060
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-40842654
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extraction
used array · 1 item
[0]
source:pmid:40842654
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agent:minimax-reader
[2] object · 4 fields
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activity-resolve-GSE63060
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accession_resolution
used array · 1 item
[0]
data:geo:GSE63060
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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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software
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agent:minimax-reader
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software
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MiniMax literature reader
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343fb30756ba6ec3
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lineage object · 4 fields
parent_id
pmid:40842654
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sha256:55d49dfeb7cbb7438392dd4664ce5627912dbada2ce88308742331eeb32b2c87
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[0]
asset:data:geo:GSE63060 licence not read
[1]
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[2]
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[3]
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[5]
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data_generation
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99e1195c7d6f
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99e1195c7d6f
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evidence array · 4 items
[0]
Myc protein concentration was measured using ELISA, and a ROC curve was constructed to assess i
[1]
man c-Myc enzyme-linked immunosorbent assay (ELISA) kit (ZC-31835) from Shanghai Zhuocai Biotec
[2]
ugh a simple and practical method like blood ELISA, we decided to focus on c-Myc in clinical ex
[3]
e instructions provided with the human c-Myc enzyme-linked immunosorbent assay (ELISA) kit (ZC-31835) from Shanghai Zhuocai
order_basis
paper_text_order:1478
id
assay:1
[1] object · 11 fields
role
analysis
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machine_learning
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f2132e96ae6c7a4e
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:40842654", "kind": "science-record", "revision": 3, "content_hash": "sha256:87d879d478d0f4a31034191e126b97efa7d17febae49ce18fe133d55d82f92d4", "created_at": "2026-11-01T20:30:56Z", "updated_at": "2026-11-01T22:14:36Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Bioinformatics and experimental validation identify biomarkers for diagnosing Alzheimer's disease.", "doi": "10.3389/fnagi.2025.1566929", "pmid": "40842654", "authors": ["Hui Liu", "Chenye Li", "Congchen Zhai", "Mei Li", "Lan Ma"], "journal": "Frontiers in aging neuroscience", "year": 2025, "abstract": "Background and purpose: Alzheimer's disease (AD) is a complex condition involving multiple mechanisms, primarily characterized by the progressive decline in cognition and memory. At present, there is no simple and reliable diagnostic method available for clinical application. Therefore, this study aims to identify potential biomarkers for AD using bioinformatics, providing new insights into its diagnosis.\nMethods: This study utilized the transcriptome dataset GSE63060 from the Gene Expression Omnibus (GEO) and applied bioinformatics approaches to identify candidate genes. Differentially expressed genes (DEGs), weighted gene co-expression network analysis (WGCNA), protein-protein interaction (PPI) networks, and machine learning techniques (LASSO, SVM-RFE, Boruta, and XGBoost) were employed on the GSE63060 dataset. Subsequently, the expression levels of the candidate genes were evaluated, and a receiver operating characteristic (ROC) curve was constructed to identify hub genes and establish a corresponding network. Finally, we focused on the common upstream transcription factor c-Myc among the hub genes and conducted clinical experiments to validate its potential. Serum samples were collected from 41 AD patients treated at the Second Affiliated Hospital of Harbin Medical University between October 2023 and November 2024, along with 41 control subjects. The c-Myc protein concentration was measured using ELISA, and a ROC curve was constructed to assess its diagnostic potential.\nResults: This study identified four hub genes associated with AD: RPL36AL, NDUFA1, NDUFS5, and RPS25. Additionally, the concentration of the c-Myc protein was significantly different between the AD and control groups (p < 0.001). The diagnostic sensitivity was 87.8%, specificity was 51.2%, and the area under the curve (AUC) value was 0.753, suggesting that c-Myc has independent diagnostic significance for AD.\nConclusion: Our study demonstrates that RPL36AL, NDUFA1, NDUFS5, and RPS25 have potential as biomarkers for the diagnosis of AD. Additionally, the experiment suggests that c-Myc could serve as a promising blood biomarker for the diagnosis of AD.", "claims": [{"id": "claim-method", "statement": "Pearson correlation analysis was performed on serum c-Myc levels, and the diagnostic value of serum c-Myc for AD was assessed using the ROC curve.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:40842654", "locator": "sections[17] \"Statistical analysis\" paragraph 2", "quote": "Pearson correlation analysis was performed on serum c-Myc levels, and the diagnostic value of serum c-Myc for AD was assessed using the ROC curve."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:40842654", "locator": "sections[38] \"Data availability statement\" paragraph 2", "quote": "The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Serum c-Myc showed diagnostic significance for Alzheimer’s disease, with 87.8% sensitivity, 51.2% specificity, and an AUC of 0.753.", "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:40842654"], "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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