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pmid:38455553

Combining WGCNA and machine learning to identify mechanisms and biomarkers of ischemic heart failure development after acute myocardial infarction.

Yan Li · Ying Hu · Feng Jiang · Haoyu Chen · Yitao Xue · Yiding Yu

Heliyon · 2024 doi:10.1016/j.heliyon.2024.e27165

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title
Combining WGCNA and machine learning to identify mechanisms and biomarkers of ischemic heart failure development after acute myocardial infarction.
doi
10.1016/j.heliyon.2024.e27165
pmid
38455553
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[0]
Yan Li
[1]
Ying Hu
[2]
Feng Jiang
[3]
Haoyu Chen
[4]
Yitao Xue
[5]
Yiding Yu
journal
Heliyon
year
2024
abstract
Background: Ischemic heart failure (IHF) is a serious complication after acute myocardial infarction (AMI). Understanding the mechanism of IHF after AMI will help us conduct early diagnosis and treatment. Methods: We obtained the AMI dataset GSE66360 and the IHF dataset GSE57338 from the GEO database, and screened overlapping genes common to both diseases through WGCNA analysis. Subsequently, we performed GO and KEGG enrichment analysis on overlapping genes to elucidate the common mechanism of AMI and IHF. Machine learning algorithms are also used to identify key biomarkers. Finally, we performed immune cell infiltration analysis on the dataset to further evaluate immune cell changes in AMI and IHF. Results: We obtained 74 overlapping genes of AMI and IHF through WGCNA analysis, and the enrichment analysis results mainly focused on immune and inflammation-related mechanisms. Through the three machine learning algorithms of LASSO, RF and SVM-RFE, we finally obtained the four Hub genes of IL1B, TIMP2, IFIT3, and P2RY2, and verified them in the IHF dataset GSE116250, and the diagnostic model AUC = 0.907. The results of immune infiltration analysis showed that 8 types of immune cells were significantly different in AMI samples, and 6 types of immune cells were significantly different in IHF samples. Conclusion: We explored the mechanism of IHF after AMI by WGCNA, enrichment analysis, and immune infiltration analysis. Four potential diagnostic candidate genes and therapeutic targets were identified by machine learning algorithms. This provides a new idea for the pathogenesis, diagnosis, and treatment of IHF after AMI.
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In this study, we employed three distinct machine learning algorithms—LASSO, Random Forest (RF), and Support Vector Machine-Recursive Feature Elimination (SVM-RFE)—to identify key hub genes associated with Acute Myocardial Infarction (AMI) and Ischemic Heart Failure (IHF).
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In this study, we employed three distinct machine learning algorithms—LASSO, Random Forest (RF), and Support Vector Machine-Recursive Feature Elimination (SVM-RFE)—to identify key hub genes associated with Acute Myocardial Infarction (AMI) and Ischemic Heart Failure (IHF).
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Publicly available datasets were analyzed in this study. This data can be found here: GSE66360; GSE57338; GSE116250.
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Publicly available datasets were analyzed in this study. This data can be found here: GSE66360; GSE57338; GSE116250.
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Through the three machine learning algorithms of LASSO, RF and SVM-RFE, we finally obtained the four Hub genes of IL1B, TIMP2, IFIT3, and P2RY2, and verified them in the IHF dataset GSE116250, and the diagnostic model AUC = 0.907.
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Through the three machine learning algorithms of LASSO, RF and SVM-RFE, we finally obtained the four Hub genes of IL1B, TIMP2, IFIT3, and P2RY2, and verified them in the IHF dataset GSE116250, and the diagnostic model AUC = 0.907.
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Through the three machine learning algorithms of LASSO, RF and SVM-RFE, we finally obtained the four Hub genes of IL1B, TIMP2, IFIT3, and P2RY2, and verified them in the IHF dataset GSE116250, and the diagnostic model AUC = 0.907.
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Through the three machine learning algorithms of LASSO, RF and SVM-RFE, we finally obtained the four Hub genes of IL1B, TIMP2, IFIT3, and P2RY2, and verified them in the IHF dataset GSE116250, and the diagnostic model AUC = 0.907.
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A Whole Blood Molecular Signature for the Identification of Acute Myocardial Infarction Without Relying Upon Myonecrosis (microarray)
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In this study, we employed three distinct machine learning algorithms—LASSO, Random Forest (RF), and Support Vector Machine-Recursive Feature Elimination (SVM-RFE)—to identify key hub genes associated with Acute Myocardial Infarction (AMI) and Ischemic Heart Failure (IHF).
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In this study, we employed three distinct machine learning algorithms—LASSO, Random Forest (RF), and Support Vector Machine-Recursive Feature Elimination (SVM-RFE)—to identify key hub genes associated with Acute Myocardial Infarction (AMI) and Ischemic Heart Failure (IHF).
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Understanding the mechanism of IHF after AMI will help us conduct early diagnosis and treatment.\nMethods: We obtained the AMI dataset GSE66360 and the IHF dataset GSE57338 from the GEO database, and screened overlapping genes common to both diseases through WGCNA analysis. Subsequently, we performed GO and KEGG enrichment analysis on overlapping genes to elucidate the common mechanism of AMI and IHF. Machine learning algorithms are also used to identify key biomarkers. Finally, we performed immune cell infiltration analysis on the dataset to further evaluate immune cell changes in AMI and IHF.\nResults: We obtained 74 overlapping genes of AMI and IHF through WGCNA analysis, and the enrichment analysis results mainly focused on immune and inflammation-related mechanisms. Through the three machine learning algorithms of LASSO, RF and SVM-RFE, we finally obtained the four Hub genes of IL1B, TIMP2, IFIT3, and P2RY2, and verified them in the IHF dataset GSE116250, and the diagnostic model AUC = 0.907. The results of immune infiltration analysis showed that 8 types of immune cells were significantly different in AMI samples, and 6 types of immune cells were significantly different in IHF samples.\nConclusion: We explored the mechanism of IHF after AMI by WGCNA, enrichment analysis, and immune infiltration analysis. Four potential diagnostic candidate genes and therapeutic targets were identified by machine learning algorithms. This provides a new idea for the pathogenesis, diagnosis, and treatment of IHF after AMI.", "claims": [{"id": "claim-method", "statement": "In this study, we employed three distinct machine learning algorithms—LASSO, Random Forest (RF), and Support Vector Machine-Recursive Feature Elimination (SVM-RFE)—to identify key hub genes associated with Acute Myocardial Infarction (AMI) and Ischemic Heart Failure (IHF).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38455553", "locator": "sections[13] \"Identification of hub genes via machine learning\" paragraph 2", "quote": "In this study, we employed three distinct machine learning algorithms—LASSO, Random Forest (RF), and Support Vector Machine-Recursive Feature Elimination (SVM-RFE)—to identify key hub genes associated with Acute Myocardial Infarction (AMI) and Ischemic Heart Failure (IHF)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Publicly available datasets were analyzed in this study. 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