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pmid:36213445

Identification of feature genes and pathways for Alzheimer's disease via WGCNA and LASSO regression.

Hongyu Sun · Jin Yang · Xiaohui Li · Yi Lyu · Zhaomeng Xu · Hui He · Xiaomin Tong · Tingyu Ji · Shihan Ding · Chaoli Zhou · Pengyong Han · Jinping Zheng

Frontiers in computational neuroscience · 2022 doi:10.3389/fncom.2022.1001546

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Experiment

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Data

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pmid:36213445
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title
Identification of feature genes and pathways for Alzheimer's disease via WGCNA and LASSO regression.
doi
10.3389/fncom.2022.1001546
pmid
36213445
authors array · 12 items
[0]
Hongyu Sun
[1]
Jin Yang
[2]
Xiaohui Li
[3]
Yi Lyu
[4]
Zhaomeng Xu
[5]
Hui He
[6]
Xiaomin Tong
[7]
Tingyu Ji
[8]
Shihan Ding
[9]
Chaoli Zhou
[10]
Pengyong Han
[11]
Jinping Zheng
journal
Frontiers in computational neuroscience
year
2022
abstract
While Alzheimer's disease (AD) can cause a severe economic burden, the specific pathogenesis involved is yet to be elucidated. To identify feature genes associated with AD, we downloaded data from three GEO databases: GSE122063, GSE15222, and GSE138260. In the filtering, we used AD for search keywords, Homo sapiens for species selection, and established a sample size of > 20 for each data set, and each data set contains Including the normal group and AD group. The datasets GSE15222 and GSE138260 were combined as a training group to build a model, and GSE122063 was used as a test group to verify the model's accuracy. The genes with differential expression found in the combined datasets were used for analysis through Gene Ontology (GO) and The Kyoto Encyclopedia of Genes and Genome Pathways (KEGG). Then, AD-related module genes were identified using the combined dataset through a weighted gene co-expression network analysis (WGCNA). Both the differential and AD-related module genes were intersected to obtain AD key genes. These genes were first filtered through LASSO regression and then AD-related feature genes were obtained for subsequent immune-related analysis. A comprehensive analysis of three AD-related datasets in the GEO database revealed 111 common differential AD genes. In the GO analysis, the more prominent terms were cognition and learning or memory. The KEGG analysis showed that these differential genes were enriched not only in In the KEGG analysis, but also in three other pathways: neuroactive ligand-receptor interaction, cAMP signaling pathway, and Calcium signaling pathway. Three AD-related feature genes (SST, MLIP, HSPB3) were finally identified. The area under the ROC curve of these AD-related feature genes was greater than 0.7 in both the training and the test groups. Finally, an immune-related analysis of these genes was performed. The finding of AD-related feature genes (SST, MLIP, HSPB3) could help predict the onset and progression of the disease. Overall, our study may provide significant guidance for further exploration of potential biomarkers for the diagnosis and prediction of AD.
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This analysis was performed using the R package “weighted gene co-expression network analysis” (WGCNA).
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sections[6] "2.4. Network construction and module identification for weighted gene co-expression network analysis (WGCNA)" paragraph 2
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This analysis was performed using the R package “weighted gene co-expression network analysis” (WGCNA).
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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/s.
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The study identified three AD-related feature genes, SST, MLIP, and HSPB3.
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Three AD-related feature genes (SST, MLIP, HSPB3) were finally identified.
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The study identified three AD-related feature genes, SST, MLIP, and HSPB3.
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[255]
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[263]
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[270]
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sample_count
363
group_sizes
null
group_sizes_basis
null
platform
2700
taxon
Homo sapiens
title
Genetic control of human brain transcript expression in Alzheimer’s disease.
resolution_checked_at
2026-11-01T18:46:34Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
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licence_read
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gaps array · 6 items
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[3]
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[4]
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[5]
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diagnostic_evaluation
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reference_standard_and_test
evidence object · 3 fields
score
0.7
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medium
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ROC curve
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id
method-2
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null
specific
null
label
Weighted gene co-expression network analysis (WGCNA)
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missing_operations array · 0 items
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evidence object · 3 fields
score
1
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quote
This analysis was performed using the R package “weighted gene co-expression network analysis” (WGCNA).
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gaps array · 1 item
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method.reader_named_unmapped
capability object · 3 fields
state
complete
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capability_id
capability:computational_analysis
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[6]
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candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
tier
R1
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nothing:replicable_now
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published_precision_envelope
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: roc.
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 · 3 items
[0]
GSE122063
[1]
GSE15222
[2]
GSE138260
resolved_accessions array · 3 items
[0]
GSE122063
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GSE15222
[2]
GSE138260
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/s.
basis
The paper names GSE122063, GSE15222, GSE138260 in GEO database 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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data:geo:GSE122063
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review object · 5 fields
state
partial
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kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
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independence
single_reader
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method
verbatim
availability
verbatim
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5
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8600
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cached_tokens
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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absent
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not_run
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paper
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source:pmid:36213445
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manuscript
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PMID 36213445 full text
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id
data:geo:GSE122063
type
dataset
label
GEO GSE122063
activities array · 3 items
[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
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id
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type
paper
label
pmid:36213445
[1] object · 3 fields
id
source:pmid:36213445
type
manuscript
label
PMID 36213445 full text
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id
data:geo:GSE122063
type
dataset
label
GEO GSE122063
agent
agent:corpus-assay-engine
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id
activity-read-36213445
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extraction
used array · 1 item
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agent
agent:minimax-reader
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id
activity-resolve-GSE122063
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accession_resolution
used array · 1 item
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data:geo:GSE122063
agent
agent:corpus-assay-engine
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agent:corpus-assay-engine
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software
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id
agent:minimax-reader
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software
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MiniMax literature reader
source_run_id
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dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
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lineage object · 4 fields
parent_id
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[3]
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36213445", "kind": "science-record", "revision": 4, "content_hash": "sha256:c2b595d9705661cf42c38268ff6f7474582574254b79f3663a2c1ec4a799e0f1", "created_at": "2026-11-01T18:15:33Z", "updated_at": "2026-11-01T22:07:47Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of feature genes and pathways for Alzheimer's disease via WGCNA and LASSO regression.", "doi": "10.3389/fncom.2022.1001546", "pmid": "36213445", "authors": ["Hongyu Sun", "Jin Yang", "Xiaohui Li", "Yi Lyu", "Zhaomeng Xu", "Hui He", "Xiaomin Tong", "Tingyu Ji", "Shihan Ding", "Chaoli Zhou", "Pengyong Han", "Jinping Zheng"], "journal": "Frontiers in computational neuroscience", "year": 2022, "abstract": "While Alzheimer's disease (AD) can cause a severe economic burden, the specific pathogenesis involved is yet to be elucidated. To identify feature genes associated with AD, we downloaded data from three GEO databases: GSE122063, GSE15222, and GSE138260. In the filtering, we used AD for search keywords, Homo sapiens for species selection, and established a sample size of > 20 for each data set, and each data set contains Including the normal group and AD group. The datasets GSE15222 and GSE138260 were combined as a training group to build a model, and GSE122063 was used as a test group to verify the model's accuracy. The genes with differential expression found in the combined datasets were used for analysis through Gene Ontology (GO) and The Kyoto Encyclopedia of Genes and Genome Pathways (KEGG). Then, AD-related module genes were identified using the combined dataset through a weighted gene co-expression network analysis (WGCNA). Both the differential and AD-related module genes were intersected to obtain AD key genes. These genes were first filtered through LASSO regression and then AD-related feature genes were obtained for subsequent immune-related analysis. A comprehensive analysis of three AD-related datasets in the GEO database revealed 111 common differential AD genes. In the GO analysis, the more prominent terms were cognition and learning or memory. The KEGG analysis showed that these differential genes were enriched not only in In the KEGG analysis, but also in three other pathways: neuroactive ligand-receptor interaction, cAMP signaling pathway, and Calcium signaling pathway. Three AD-related feature genes (SST, MLIP, HSPB3) were finally identified. The area under the ROC curve of these AD-related feature genes was greater than 0.7 in both the training and the test groups. Finally, an immune-related analysis of these genes was performed. The finding of AD-related feature genes (SST, MLIP, HSPB3) could help predict the onset and progression of the disease. Overall, our study may provide significant guidance for further exploration of potential biomarkers for the diagnosis and prediction of AD.", "claims": [{"id": "claim-method", "statement": "This analysis was performed using the R package “weighted gene co-expression network analysis” (WGCNA).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36213445", "locator": "sections[6] \"2.4. Network construction and module identification for weighted gene co-expression network analysis (WGCNA)\" paragraph 2", "quote": "This analysis was performed using the R package “weighted gene co-expression network analysis” (WGCNA)."}], "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/s.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36213445", "locator": "sections[19] \"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/s."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The study identified three AD-related feature genes, SST, MLIP, and HSPB3.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:36213445", "locator": "sections[0] \"Abstract\" paragraph 1", "quote": "Three AD-related feature genes (SST, MLIP, HSPB3) were finally identified."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The study identified three AD-related feature genes, SST, MLIP, and HSPB3.", "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:36213445"], "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:GSE122063"], "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:GSE122063"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:36213445", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fncom.2022.1001546", "sha256": "sha256:7ba3cf9e93418e4a1eabd303c58c552ec377aeda3ae4b049edcc6564aab77403", "bytes": 27344, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fncom.2022.1001546", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC9536257", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE122063", "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=GSE122063", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE122063", "version": null, "note": "The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.", "access_statement_kind": "data_availability_statement", "sample_accessions": ["GSM3454053", "GSM3454054", "GSM3454055", "GSM3454056", "GSM3454057", "GSM3454058", "GSM3454059", "GSM3454060", "GSM3454061", "GSM3454062", "GSM3454063", "GSM3454064", "GSM3454065", "GSM3454066", "GSM3454067", "GSM3454068", "GSM3454069", "GSM3454070", "GSM3454071", "GSM3454072", "GSM3454073", "GSM3454074", "GSM3454075", "GSM3454076", "GSM3454077", "GSM3454078", "GSM3454079", "GSM3454080", "GSM3454081", "GSM3454082", "GSM3454083", "GSM3454084", "GSM3454085", "GSM3454086", "GSM3454087", "GSM3454088", "GSM3454089", "GSM3454090", "GSM3454091", "GSM3454092", "GSM3454093", "GSM3454094", "GSM3454095", 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