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pmid:37251077

Exploring the shared gene signatures of smoking-related osteoporosis and chronic obstructive pulmonary disease using machine learning algorithms.

Haotian Wang · Shaoshuo Li · Baixing Chen · Mao Wu · Heng Yin · Yang Shao · Jianwei Wang

Frontiers in molecular biosciences · 2023 doi:10.3389/fmolb.2023.1204031

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title
Exploring the shared gene signatures of smoking-related osteoporosis and chronic obstructive pulmonary disease using machine learning algorithms.
doi
10.3389/fmolb.2023.1204031
pmid
37251077
authors array · 7 items
[0]
Haotian Wang
[1]
Shaoshuo Li
[2]
Baixing Chen
[3]
Mao Wu
[4]
Heng Yin
[5]
Yang Shao
[6]
Jianwei Wang
journal
Frontiers in molecular biosciences
year
2023
abstract
Objectives: Cigarette smoking has been recognized as a predisposing factor for both osteoporosis (OP) and chronic obstructive pulmonary disease (COPD). This study aimed to investigate the shared gene signatures affected by cigarette smoking in OP and COPD through gene expression profiling. Materials and methods: Microarray datasets (GSE11784, GSE13850, GSE10006, and GSE103174) were obtained from Gene Expression Omnibus (GEO) and analyzed for differentially expressed genes (DEGs) and weighted gene co-expression network analysis (WGCNA). Least absolute shrinkage and selection operator (LASSO) regression method and a random forest (RF) machine learning algorithm were used to identify candidate biomarkers. The diagnostic value of the method was assessed using logistic regression and receiver operating characteristic (ROC) curve analysis. Finally, immune cell infiltration was analyzed to identify dysregulated immune cells in cigarette smoking-induced COPD. Results: In the smoking-related OP and COPD datasets, 2858 and 280 DEGs were identified, respectively. WGCNA revealed 982 genes strongly correlated with smoking-related OP, of which 32 overlapped with the hub genes of COPD. Gene Ontology (GO) enrichment analysis showed that the overlapping genes were enriched in the immune system category. Using LASSO regression and RF machine learning, six candidate genes were identified, and a logistic regression model was constructed, which had high diagnostic values for both the training set and external validation datasets. The area under the curves (AUCs) were 0.83 and 0.99, respectively. Immune cell infiltration analysis revealed dysregulation in several immune cells, and six immune-associated genes were identified for smoking-related OP and COPD, namely, mucosa-associated lymphoid tissue lymphoma translocation protein 1 (MALT1), tissue-type plasminogen activator (PLAT), sodium channel 1 subunit alpha (SCNN1A), sine oculis homeobox 3 (SIX3), sperm-associated antigen 9 (SPAG9), and vacuolar protein sorting 35 (VPS35). Conclusion: The findings suggest that immune cell infiltration profiles play a significant role in the shared pathogenesis of smoking-related OP and COPD. The results could provide valuable insights for developing novel therapeutic strategies for managing these disorders, as well as shedding light on their pathogenesis.
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The DEGs were identified using the limma package in R (version 4.1.1; http://cran.r-project.org/) (Ritchie et al., 2015), and subsequently analyzed using different packages.
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sections[4] "2.2 Data processing and analysis of differential gene expression" paragraph 2
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The DEGs were identified using the limma package in R (version 4.1.1; http://cran.r-project.org/) (Ritchie et al., 2015), and subsequently analyzed using different packages.
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Using microarray data obtained from GEO and analyzed with differential gene expression and WGCNA approaches, the study identified six shared candidate genes and constructed a logistic regression model with reported AUCs of 0.83 and 0.99.
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Microarray datasets (GSE11784, GSE13850, GSE10006, and GSE103174) were obtained from Gene Expression Omnibus (GEO) and analyzed for differentially expressed genes (DEGs) and weighted gene co-expression network analysis (WGCNA).
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Using LASSO regression and RF machine learning, six candidate genes were identified, and a logistic regression model was constructed, which had high diagnostic values for both the training set and external validation datasets.
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The area under the curves (AUCs) were 0.83 and 0.99, respectively.
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Using microarray data obtained from GEO and analyzed with differential gene expression and WGCNA approaches, the study identified six shared candidate genes and constructed a logistic regression model with reported AUCs of 0.83 and 0.99.
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[3]
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[4]
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[5]
asset:data:geo:GSE11784 licence not read
[6]
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[7]
asset:data:geo:GSE13850 licence not read
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state
complete
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limma_voom
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count_matrix_with_condition
evidence object · 3 fields
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1
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quote
The DEGs were identified using the limma package in R (version 4.1.1; http://cran.r-project.org/) (Ritchie et al., 2015), and subsequently analyzed using different packages.
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random_forest
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machine_learning_random_forest
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false
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labelled_feature_matrix
evidence object · 3 fields
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0.7
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random forest
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method-3
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regression_modelling
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Regression modelling
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evidence object · 3 fields
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0.7
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Network / pathway analysis
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diagnostic_evaluation
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label
Diagnostic test evaluation
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0.8
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capability object · 3 fields
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complete
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capability_id
capability:computational_analysis
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gwas
candidate
Automated Assays Laravel application and simulated adapters
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complete
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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
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capability:computational_analysis
availability_state
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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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[0]
GSE11784
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GSE13850
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GSE10006
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[0]
GSE11784
[1]
GSE13850
[2]
GSE10006
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GSE103174
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 authors.
basis
The paper names GSE11784, GSE13850, GSE10006, GSE103174 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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source:pmid:37251077
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data:geo:GSE10006
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run_analysis
must_build object · 5 fields
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data:geo:GSE10006
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review object · 5 fields
state
partial
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extraction_review
reader object · 5 fields
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MiniMax-M3.1-Flash
provider
minimax
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minimax
read_at
2026-11-01T18:42:14Z
independence
single_reader
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verbatim
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10007
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1778
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264
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extraction
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complete
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not_run
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provenance object · 7 fields
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[0] object · 3 fields
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pmid:37251077
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paper
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pmid:37251077
[1] object · 3 fields
id
source:pmid:37251077
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manuscript
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PMID 37251077 full text
[2] object · 3 fields
id
data:geo:GSE10006
type
dataset
label
GEO GSE10006
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id
activity-reading-sci-2026-11-01
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classification
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paper
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pmid:37251077
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source:pmid:37251077
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manuscript
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PMID 37251077 full text
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data:geo:GSE10006
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dataset
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GEO GSE10006
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agent:corpus-assay-engine
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extraction
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agent:minimax-reader
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agent:corpus-assay-engine
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agent:corpus-assay-engine
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agent:minimax-reader
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343fb30756ba6ec3
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lineage object · 4 fields
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[5]
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expression profiling. Materials and methods: Microarray datasets (GSE11784, GSE13850, GSE10006, and
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37251077", "kind": "science-record", "revision": 4, "content_hash": "sha256:21eae84e20b181c50ad313c5d6a9b6ff00482fc2193a6619076cf2029aa964c0", "created_at": "2026-11-01T19:01:57Z", "updated_at": "2026-11-01T22:52:01Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Exploring the shared gene signatures of smoking-related osteoporosis and chronic obstructive pulmonary disease using machine learning algorithms.", "doi": "10.3389/fmolb.2023.1204031", "pmid": "37251077", "authors": ["Haotian Wang", "Shaoshuo Li", "Baixing Chen", "Mao Wu", "Heng Yin", "Yang Shao", "Jianwei Wang"], "journal": "Frontiers in molecular biosciences", "year": 2023, "abstract": "Objectives: Cigarette smoking has been recognized as a predisposing factor for both osteoporosis (OP) and chronic obstructive pulmonary disease (COPD). This study aimed to investigate the shared gene signatures affected by cigarette smoking in OP and COPD through gene expression profiling. Materials and methods: Microarray datasets (GSE11784, GSE13850, GSE10006, and GSE103174) were obtained from Gene Expression Omnibus (GEO) and analyzed for differentially expressed genes (DEGs) and weighted gene co-expression network analysis (WGCNA). Least absolute shrinkage and selection operator (LASSO) regression method and a random forest (RF) machine learning algorithm were used to identify candidate biomarkers. The diagnostic value of the method was assessed using logistic regression and receiver operating characteristic (ROC) curve analysis. Finally, immune cell infiltration was analyzed to identify dysregulated immune cells in cigarette smoking-induced COPD. Results: In the smoking-related OP and COPD datasets, 2858 and 280 DEGs were identified, respectively. WGCNA revealed 982 genes strongly correlated with smoking-related OP, of which 32 overlapped with the hub genes of COPD. Gene Ontology (GO) enrichment analysis showed that the overlapping genes were enriched in the immune system category. Using LASSO regression and RF machine learning, six candidate genes were identified, and a logistic regression model was constructed, which had high diagnostic values for both the training set and external validation datasets. The area under the curves (AUCs) were 0.83 and 0.99, respectively. Immune cell infiltration analysis revealed dysregulation in several immune cells, and six immune-associated genes were identified for smoking-related OP and COPD, namely, mucosa-associated lymphoid tissue lymphoma translocation protein 1 (MALT1), tissue-type plasminogen activator (PLAT), sodium channel 1 subunit alpha (SCNN1A), sine oculis homeobox 3 (SIX3), sperm-associated antigen 9 (SPAG9), and vacuolar protein sorting 35 (VPS35). Conclusion: The findings suggest that immune cell infiltration profiles play a significant role in the shared pathogenesis of smoking-related OP and COPD. The results could provide valuable insights for developing novel therapeutic strategies for managing these disorders, as well as shedding light on their pathogenesis.", "claims": [{"id": "claim-method", "statement": "The DEGs were identified using the limma package in R (version 4.1.1; http://cran.r-project.org/) (Ritchie et al., 2015), and subsequently analyzed using different packages.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37251077", "locator": "sections[4] \"2.2 Data processing and analysis of differential gene expression\" paragraph 2", "quote": "The DEGs were identified using the limma package in R (version 4.1.1; http://cran.r-project.org/) (Ritchie et al., 2015), and subsequently analyzed using different packages."}], "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 authors.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37251077", "locator": "sections[20] \"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 authors."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Using microarray data obtained from GEO and analyzed with differential gene expression and WGCNA approaches, the study identified six shared candidate genes and constructed a logistic regression model with reported AUCs of 0.83 and 0.99.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37251077", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "Microarray datasets (GSE11784, GSE13850, GSE10006, and GSE103174) were obtained from Gene Expression Omnibus (GEO) and analyzed for differentially expressed genes (DEGs) and weighted gene co-expression network analysis (WGCNA)."}, {"asset": "source:pmid:37251077", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "Using LASSO regression and RF machine learning, six candidate genes were identified, and a logistic regression model was constructed, which had high diagnostic values for both the training set and external validation datasets."}, {"asset": "source:pmid:37251077", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "The area under the curves (AUCs) were 0.83 and 0.99, respectively."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Using microarray data obtained from GEO and analyzed with differential gene expression and WGCNA approaches, the study identified six shared candidate genes and constructed a logistic regression model with reported AUCs of 0.83 and 0.99.", "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:37251077"], "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:GSE10006"], "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:GSE10006"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:37251077", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fmolb.2023.1204031", "sha256": 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