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pmid:36345357
In Silico Identification of Key Genes and Immune Infiltration Characteristics in Epicardial Adipose Tissue from Patients with Coronary Artery Disease.
Yisen Deng · Xuming Wang · Zhan Liu · Xiaoshuo Lv · Bo Ma · Qiangqiang Nie · Xueqiang Fan · Yuguang Yang · Zhidong Ye · Peng Liu · Jianyan Wen
BioMed research international · 2022 doi:10.1155/2022/5610317
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Experiment
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Complete file
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We also explored potential biomarkers using two machine-learning algorithms and calculated the immune cell infiltration in EAT.\nMaterials and Methods: Three datasets (GSE120774, GSE64554, and GSE24425) were obtained from the Gene Expression Omnibus (GEO) database. The GSE120774 dataset was used to evaluate DEGs between EAT of CAD patients and the control group. Functional enrichment analyses were conducted to study associated biological functions and mechanisms using the Kyoto Encyclopedia of Genes and Genomes (KEGG), Gene Ontology (GO), and Gene Set Enrichment Analysis (GSEA). After this, the least absolute shrinkage and selection operator (LASSO) and support vector machine recursive feature elimination (SVM-RFE) were performed to identify the feature genes related to CAD. The expression level of the feature genes was validated in GSE64554 and GSE24425. Finally, we calculated the immune cell infiltration and evaluated the correlation between the feature genes and immune cells using CIBERSORT.\nResults: We identified a total of 130 upregulated and 107 downregulated genes in GSE120774. Functional enrichment analysis revealed that DEGs are associated with several pathways, including the calcium signaling pathway, complement and coagulation cascades, ferroptosis, fluid shear stress and atherosclerosis, lipid and atherosclerosis, and regulation of lipolysis in adipocytes. TCF21, CDH19, XG, and NNAT were identified as feature genes and validated in the GSE64554 and GSE24425 datasets. Immune cell infiltration analysis showed plasma cells are significantly more numerous in EAT than in the control group (p = 0.001), whereas macrophage M0 (p = 0.024) and resting mast cells (p = 0.036) were significantly less numerous. TCF21, CDH19, XG, and NNAT were correlated with immune cells, including plasma cells, M0 macrophages, and resting mast cells.\nConclusion: TCF21, CDH19, XG, and NNAT might serve as feature genes for CAD, providing new insights for future research on the pathogenesis of cardiovascular diseases.", "claims": [{"id": "claim-method", "statement": "The DEGs were identified by the limma package in R.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36345357", "locator": "sections[4] \"2.2. Identification of Differentially Expressed Genes\" paragraph 2", "quote": "The DEGs were identified by the limma package in R."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All the analyses in this study were based on the publicly available datasets (GSE120774, GSE64554, and GSE24425). 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