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pmid:36642989

Identifying effective diagnostic biomarkers and immune infiltration features in chronic kidney disease by bioinformatics and validation.

Tao Liu · Xing Xing Zhuang · Xiu Juan Qin · Liang Bing Wei · Jia Rong Gao

Frontiers in pharmacology · 2022 doi:10.3389/fphar.2022.1069810

Paper

complete

Experiment

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Data

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Analysis

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Execution

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title
Identifying effective diagnostic biomarkers and immune infiltration features in chronic kidney disease by bioinformatics and validation.
doi
10.3389/fphar.2022.1069810
pmid
36642989
authors array · 5 items
[0]
Tao Liu
[1]
Xing Xing Zhuang
[2]
Xiu Juan Qin
[3]
Liang Bing Wei
[4]
Jia Rong Gao
journal
Frontiers in pharmacology
year
2022
abstract
Background: Chronic kidney disease (CKD), characterized by sustained inflammation and immune dysfunction, is highly prevalent and can eventually progress to end-stage kidney disease. However, there is still a lack of effective and reliable diagnostic markers and therapeutic targets for CKD. Methods: First, we merged data from GEO microarrays (GSE104948 and GSE116626) to identify differentially expressed genes (DEGs) in CKD and healthy patient samples. Then, we conducted GO, KEGG, HPO, and WGCNA analyses to explore potential functions of DEGs and select clinically significant modules. Moreover, STRING was used to analyse protein-protein interactions. CytoHubba and MCODE algorithms in the cytoscape plug-in were performed to screen hub genes in the network. We then determined the diagnostic significance of the obtained hub genes by ROC and two validation datasets. Meanwhile, the expression level of the biomarkers was verified by IHC. Furthermore, we examined immunological cells' relationships with hub genes. Finally, GSEA was conducted to determine the biological functions that biomarkers are significantly enriched. STITCH and AutoDock Vina were used to predict and validate drug-gene interactions. Results: A total of 657 DEGs were screened and functional analysis emphasizes their important role in inflammatory responses and immunomodulation in CKD. Through WGCNA, the interaction network, ROC curves, and validation set, four hub genes (IL10RA, CD45, CTSS, and C1QA) were identified. Furthermore, IHC of CKD patients confirmed the results above. Immune infiltration analysis indicated that CKD had a significant increase in monocytes, M0 macrophages, and M1 macrophages but a decrease in regulatory T cells, activated dendritic cells, and so on. Moreover, four hub genes were statistically correlated with them. Further analysis exhibited that IL10RA, which obtained the highest expression level in hub genes, was involved in abnormalities in various immune cells and regulated a large number of immune system responses and inflammation-related pathways. In addition, the drug-gene interaction network contained four potential therapeutic drugs targeting IL10RA, and molecular docking might make this relationship viable. Conclusion: IL10RA and its related hub molecules might play a key role in the development of CKD and could be potential biomarkers in CKD.
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We conducted ROC analysis to study the relationship between hub gene expression and the prognosis of CKD patients (Supplementary File S15).
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sections[18] "3.5 Diagnostic value and validation of hub gene on CKD" paragraph 2
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We conducted ROC analysis to study the relationship between hub gene expression and the prognosis of CKD patients (Supplementary File S15).
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sections[27] "Data availability statement" paragraph 2
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
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The study identified four CKD hub genes—IL10RA, CD45, CTSS, and C1QA—with high diagnostic value.
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Through WGCNA, the interaction network, ROC curves, and validation set, four hub genes (IL10RA, CD45, CTSS, and C1QA) were identified.
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The study identified four CKD hub genes—IL10RA, CD45, CTSS, and C1QA—with high diagnostic value.
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title
Transcriptomic and proteomic profiling reveal insights of mesangial cell function in patients with IgA Nephropathy
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sion level of the biomarkers was verified by IHC. Furthermore, we examined immunological cell
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TSS, and C1QA) were identified. Furthermore, IHC of CKD patients confirmed the results above.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36642989", "kind": "science-record", "revision": 4, "content_hash": "sha256:9afec3303f85b4470151bd89b270d603882a859c9b12fd2552e353862cc3eaf0", "created_at": "2026-11-01T19:01:11Z", "updated_at": "2026-11-01T22:51:02Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identifying effective diagnostic biomarkers and immune infiltration features in chronic kidney disease by bioinformatics and validation.", "doi": "10.3389/fphar.2022.1069810", "pmid": "36642989", "authors": ["Tao Liu", "Xing Xing Zhuang", "Xiu Juan Qin", "Liang Bing Wei", "Jia Rong Gao"], "journal": "Frontiers in pharmacology", "year": 2022, "abstract": "Background: Chronic kidney disease (CKD), characterized by sustained inflammation and immune dysfunction, is highly prevalent and can eventually progress to end-stage kidney disease. However, there is still a lack of effective and reliable diagnostic markers and therapeutic targets for CKD. Methods: First, we merged data from GEO microarrays (GSE104948 and GSE116626) to identify differentially expressed genes (DEGs) in CKD and healthy patient samples. Then, we conducted GO, KEGG, HPO, and WGCNA analyses to explore potential functions of DEGs and select clinically significant modules. Moreover, STRING was used to analyse protein-protein interactions. CytoHubba and MCODE algorithms in the cytoscape plug-in were performed to screen hub genes in the network. We then determined the diagnostic significance of the obtained hub genes by ROC and two validation datasets. Meanwhile, the expression level of the biomarkers was verified by IHC. Furthermore, we examined immunological cells' relationships with hub genes. Finally, GSEA was conducted to determine the biological functions that biomarkers are significantly enriched. STITCH and AutoDock Vina were used to predict and validate drug-gene interactions. Results: A total of 657 DEGs were screened and functional analysis emphasizes their important role in inflammatory responses and immunomodulation in CKD. Through WGCNA, the interaction network, ROC curves, and validation set, four hub genes (IL10RA, CD45, CTSS, and C1QA) were identified. Furthermore, IHC of CKD patients confirmed the results above. Immune infiltration analysis indicated that CKD had a significant increase in monocytes, M0 macrophages, and M1 macrophages but a decrease in regulatory T cells, activated dendritic cells, and so on. Moreover, four hub genes were statistically correlated with them. Further analysis exhibited that IL10RA, which obtained the highest expression level in hub genes, was involved in abnormalities in various immune cells and regulated a large number of immune system responses and inflammation-related pathways. In addition, the drug-gene interaction network contained four potential therapeutic drugs targeting IL10RA, and molecular docking might make this relationship viable. Conclusion: IL10RA and its related hub molecules might play a key role in the development of CKD and could be potential biomarkers in CKD.", "claims": [{"id": "claim-method", "statement": "We conducted ROC analysis to study the relationship between hub gene expression and the prognosis of CKD patients (Supplementary File S15).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36642989", "locator": "sections[18] \"3.5 Diagnostic value and validation of hub gene on CKD\" paragraph 2", "quote": "We conducted ROC analysis to study the relationship between hub gene expression and the prognosis of CKD patients (Supplementary File S15)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets presented in this study can be found in online repositories. 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