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pmid:38312744
Identification of apoptosis-related gene signatures as potential biomarkers for differentiating active from latent tuberculosis via bioinformatics analysis.
Xiaoting Dai · Litian Zhou · Xiaopu He · Jie Hua · Liang Chen · Yingying Lu
Frontiers in cellular and infection microbiology · 2024 doi:10.3389/fcimb.2024.1285493
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Experiment
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Analysis
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Complete file
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This study aims to identify apoptosis-related genes as biomarkers for differentiating active tuberculosis (ATB) from latent tuberculosis infection (LTBI).\nMethods: The tuberculosis (TB) datasets (GSE19491, GSE62525, and GSE28623) were downloaded from the Gene Expression Omnibus (GEO) database. The diagnostic biomarkers differentiating ATB from LTBI were identified by combining the data of protein-protein interaction network, differentially expressed gene, Weighted Gene Co-Expression Network Analysis (WGCNA), and receiver operating characteristic (ROC) analyses. Machine learning algorithms were employed to validate the diagnostic ability of the biomarkers. Enrichment analysis for biomarkers was established, and potential drugs were predicted. The association between biomarkers and N6-methyladenosine (m6A) or 5-methylated cytosine (m5C) regulators was evaluated.\nResults: Six biomarkers including CASP1, TNFSF10, CASP4, CASP5, IFI16, and ATF3 were obtained for differentiating ATB from LTBI. They showed strong diagnostic performances, with area under ROC (AUC) values > 0.7. Enrichment analysis demonstrated that the biomarkers were involved in immune and inflammation responses. Furthermore, 24 drugs, including progesterone and emricasan, were predicted. The correlation analysis revealed that biomarkers were positively correlated with most m6A or m5C regulators.\nConclusion: The six ARGs can serve as effective biomarkers differentiating ATB from LTBI and provide insight into the pathogenesis of Mycobacterium tuberculosis infection.", "claims": [{"id": "claim-method", "statement": "The diagnostic ability of the biomarkers was assessed via the ROC, and validation sets were validated.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38312744", "locator": "sections[7] \"Assessment of the diagnostic value of biomarkers for ATB and qRT-PCR\" paragraph 2", "quote": "The diagnostic ability of the biomarkers was assessed via the ROC, and validation sets were validated."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets presented in this study can be found in online repositories. 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