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pmid:38469146

Identification of important modules and biomarkers in diabetic cardiomyopathy based on WGCNA and LASSO analysis.

Min Cui · Hao Wu · Yajuan An · Yue Liu · Liping Wei · Xin Qi

Frontiers in endocrinology · 2024 doi:10.3389/fendo.2024.1185062

Paper

complete

Experiment

partial

Data

partial

Analysis

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Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:38469146
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title
Identification of important modules and biomarkers in diabetic cardiomyopathy based on WGCNA and LASSO analysis.
doi
10.3389/fendo.2024.1185062
pmid
38469146
authors array · 6 items
[0]
Min Cui
[1]
Hao Wu
[2]
Yajuan An
[3]
Yue Liu
[4]
Liping Wei
[5]
Xin Qi
journal
Frontiers in endocrinology
year
2024
abstract
Background: Diabetic cardiomyopathy (DCM) lacks specific and sensitive biomarkers, and its diagnosis remains a challenge. Therefore, there is an urgent need to develop useful biomarkers to help diagnose and evaluate the prognosis of DCM. This study aims to find specific diagnostic markers for diabetic cardiomyopathy. Methods: Two datasets (GSE106180 and GSE161827) from the GEO database were integrated to identify differentially expressed genes (DEGs) between control and type 2 diabetic cardiomyopathy. We assessed the infiltration of immune cells and used weighted coexpression network analysis (WGCNA) to construct the gene coexpression network. Then we performed a clustering analysis. Finally, a diagnostic model was built by the least absolute shrinkage and selection operator (LASSO). Results: A total of 3066 DEGs in the GSE106180 and GSE161827 datasets. There were differences in immune cell infiltration. According to gene significance (GS) > 0.2 and module membership (MM) > 0.8, 41 yellow Module genes and 1474 turquoise Module genes were selected. Hub genes were mainly related to the "proteasomal protein catabolic process", "mitochondrial matrix" and "protein processing in endoplasmic reticulum" pathways. LASSO was used to construct a diagnostic model composed of OXCT1, CACNA2D2, BCL7B, EGLN3, GABARAP, and ACADSB and verified it in the GSE163060 and GSE175988 datasets with AUCs of 0.9333 (95% CI: 0.7801-1) and 0.96 (95% CI: 0.8861-1), respectively. H9C2 cells were verified, and the results were similar to the bioinformatics analysis. Conclusion: We constructed a diagnostic model of DCM, and OXCT1, CACNA2D2, BCL7B, EGLN3, GABARAP, and ACADSB were potential biomarkers, which may provide new insights for improving the ability of early diagnosis and treatment of diabetic cardiomyopathy.
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Then, we established a LASSO model with these selected genes based on the value of lambda (minλ= 0.00457) ( Figures 6B, C ).
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Then, we established a LASSO model with these selected genes based on the value of lambda (minλ= 0.00457) ( Figures 6B, C ).
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sections[24] "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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LASSO was used to construct a diagnostic model composed of OXCT1, CACNA2D2, BCL7B, EGLN3, GABARAP, and ACADSB and verified it in the GSE163060 and GSE175988 datasets with AUCs of 0.9333 (95% CI: 0.7801-1) and 0.96 (95% CI: 0.8861-1), respectively.
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LASSO was used to construct a diagnostic model composed of OXCT1, CACNA2D2, BCL7B, EGLN3, GABARAP, and ACADSB and verified it in the GSE163060 and GSE175988 datasets with AUCs of 0.9333 (95% CI: 0.7801-1) and 0.96 (95% CI: 0.8861-1), respectively.
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LASSO was used to construct a diagnostic model composed of OXCT1, CACNA2D2, BCL7B, EGLN3, GABARAP, and ACADSB and verified it in the GSE163060 and GSE175988 datasets with AUCs of 0.9333 (95% CI: 0.7801-1) and 0.96 (95% CI: 0.8861-1), respectively.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38469146", "kind": "science-record", "revision": 4, "content_hash": "sha256:19b432959303ac809466425400dfd95ea2a36c3f4589395305e91f08e0d78714", "created_at": "2026-11-01T19:20:25Z", "updated_at": "2026-11-01T22:11:26Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of important modules and biomarkers in diabetic cardiomyopathy based on WGCNA and LASSO analysis.", "doi": "10.3389/fendo.2024.1185062", "pmid": "38469146", "authors": ["Min Cui", "Hao Wu", "Yajuan An", "Yue Liu", "Liping Wei", "Xin Qi"], "journal": "Frontiers in endocrinology", "year": 2024, "abstract": "Background: Diabetic cardiomyopathy (DCM) lacks specific and sensitive biomarkers, and its diagnosis remains a challenge. Therefore, there is an urgent need to develop useful biomarkers to help diagnose and evaluate the prognosis of DCM. This study aims to find specific diagnostic markers for diabetic cardiomyopathy.\nMethods: Two datasets (GSE106180 and GSE161827) from the GEO database were integrated to identify differentially expressed genes (DEGs) between control and type 2 diabetic cardiomyopathy. We assessed the infiltration of immune cells and used weighted coexpression network analysis (WGCNA) to construct the gene coexpression network. Then we performed a clustering analysis. Finally, a diagnostic model was built by the least absolute shrinkage and selection operator (LASSO).\nResults: A total of 3066 DEGs in the GSE106180 and GSE161827 datasets. There were differences in immune cell infiltration. According to gene significance (GS) > 0.2 and module membership (MM) > 0.8, 41 yellow Module genes and 1474 turquoise Module genes were selected. Hub genes were mainly related to the \"proteasomal protein catabolic process\", \"mitochondrial matrix\" and \"protein processing in endoplasmic reticulum\" pathways. LASSO was used to construct a diagnostic model composed of OXCT1, CACNA2D2, BCL7B, EGLN3, GABARAP, and ACADSB and verified it in the GSE163060 and GSE175988 datasets with AUCs of 0.9333 (95% CI: 0.7801-1) and 0.96 (95% CI: 0.8861-1), respectively. H9C2 cells were verified, and the results were similar to the bioinformatics analysis.\nConclusion: We constructed a diagnostic model of DCM, and OXCT1, CACNA2D2, BCL7B, EGLN3, GABARAP, and ACADSB were potential biomarkers, which may provide new insights for improving the ability of early diagnosis and treatment of diabetic cardiomyopathy.", "claims": [{"id": "claim-method", "statement": "Then, we established a LASSO model with these selected genes based on the value of lambda (minλ= 0.00457) ( Figures 6B, C ).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38469146", "locator": "sections[19] \"Screening the diagnostic markers\" paragraph 2", "quote": "Then, we established a LASSO model with these selected genes based on the value of lambda (minλ= 0.00457) ( Figures 6B, C )."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/supplementary material. 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