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pmid:36213260
A novel prognostic 6-gene signature for osteoporosis.
Yu Zhao · Jieping Yan · Yimiao Zhu · Zhenping Han · Tingting Li · Lijuan Wang
Frontiers in endocrinology · 2022 doi:10.3389/fendo.2022.968397
Paper
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Experiment
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Data
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Analysis
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Execution
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Complete file
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Therefore, identifying the diagnostic and prognostic biomarkers of OP is of great significance.\nMethods: mRNA data from OP and non-OP samples were obtained from GEO database, which were divided into training set (GSE35959) and testing sets (GSE7158, GSE62402, GSE7429 and GSE56815). Gene modules most significantly related to OP were revealed using weighted gene co-expression network analysis (WGCNA) and differentially expressed genes (DEGs) between OP and normal samples in training set were identified using limma R package. Thereafter, above two gene sets were intersected to obtain the genes potentially related to OP. Protein-protein interaction (PPI) pairs were screened by STRING database and visualized using Cytoscape, while the plug-in cytoHubba was used to screen hub genes by determining their topological parameters. Afterwards, a diagnostic model was constructed using those hub genes, whose creditability was further evaluated by testing sets.\nResults: The results of WGCNA analysis found the Black module was most significantly related to OP, which included altogether 1286 genes. Meanwhile, 2771 DEGs were discovered between OP patients and the normal controls. After taking the intersection, 479 genes were identified potentially correlated with the development of OP. Subsequently, six hub genes were discovered through PPI network construction and node topological analysis. Finally, we constructed a support vector machine model based on these six genes, which can accurately classified training and testing set samples into OP and normal groups.\nConclusion: Our current study constructed a six hub genes-based diagnostic model for OP. 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