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pmid:40470717

Tracing the molecular landscape of diabetic nephropathy: Insights from machine learning and experiment verification.

Shahad W Kattan · Ahmed M Basri · Mohammad H Alhashmi · Amany I Almars · Reem Hasaballah Alhasani · Ifat Alsharif · Ikhlas A Sindi · Ahmad H Mufti · Iman S Abumansour · Nasser A Elhawary · Aishah Abdullah Qahtani · Hailah M Almohaimeed

Journal of diabetes investigation · 2025 doi:10.1111/jdi.70026

Paper

complete

Experiment

partial

Data

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Analysis

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Execution

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:40470717
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science-record
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2026-11-01T20:30:35Z
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paper object · 10 fields
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title
Tracing the molecular landscape of diabetic nephropathy: Insights from machine learning and experiment verification.
doi
10.1111/jdi.70026
pmid
40470717
authors array · 12 items
[0]
Shahad W Kattan
[1]
Ahmed M Basri
[2]
Mohammad H Alhashmi
[3]
Amany I Almars
[4]
Reem Hasaballah Alhasani
[5]
Ifat Alsharif
[6]
Ikhlas A Sindi
[7]
Ahmad H Mufti
[8]
Iman S Abumansour
[9]
Nasser A Elhawary
[10]
Aishah Abdullah Qahtani
[11]
Hailah M Almohaimeed
journal
Journal of diabetes investigation
year
2025
abstract
OBJECTIVE: Diabetes is a chronic disease resulting from insufficient insulin secretion or impaired insulin function. Diabetic nephropathy (DN) is one of the most common complications of diabetes and a leading cause of end-stage renal disease. Early diagnosis of DN is crucial for timely intervention and effective disease management. METHODS: Gene expression profiles GSE142025 and GSE220226 were retrieved from the GEO database and combined into a metadata cohort, while GSE189007 was obtained as an independent validation dataset. Differentially expressed genes (DEGs) were identified in 46 glomerular samples from DN patients and 31 control samples. Gene Ontology (GO) and Disease Ontology (DO) enrichment analyses, gene set enrichment analysis (GSEA), least absolute shrinkage and selection operator (LASSO) regression, support vector machine-recursive feature elimination (SVM-RFE) analysis, and area under the curve (AUC) calculations were performed. RESULTS: A total of 109 DEGs were identified. Among them, DUSP1, EGR1, FPR1, G6PC, GDF15, LOX, LPL, PRKAR2B, PTGDS, and TPPP3 were selected as potential diagnostic biomarkers for DN. These biomarkers exhibited a positive correlation with immune cell infiltration. Experimental validation identified LOX as the most promising novel diagnostic biomarker for DN. This study provides new insights into the early diagnosis, pathogenesis, and molecular mechanisms of DN.
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DEGs were screened using the least absolute shrinkage and selection operator (LASSO) regression model for variable selection and regularization, reducing overfitting and improving predictive accuracy.
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The DN Glomeruli and Control datasets, GSE142025 31 and GSE220226 32 , were downloaded from the Gene Expression Omnibus (GEO) database.
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Experimental validation identified LOX as the most promising novel diagnostic biomarker for DN.
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Experimental validation identified LOX as the most promising novel diagnostic biomarker for DN.
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Comparison of Kidney Transcriptomic Profiles of Early and Advanced Diabetic Nephropathy Reveals Potential New Mechanisms for Disease Progression
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Gene-expression profiles of whole blood cells from a Han Chinese population with or without Type-2 Diabetes Mellitus or/and its complications in nephropathy and retinopathy
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asset:data:geo:GSE189007 licence not read
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:40470717", "kind": "science-record", "revision": 3, "content_hash": "sha256:0ec6a92f9fe6b0e3a53a8d15cd6ae0c42b9a491a53caece2cfaf637696fa8339", "created_at": "2026-11-01T20:30:35Z", "updated_at": "2026-11-01T22:14:09Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Tracing the molecular landscape of diabetic nephropathy: Insights from machine learning and experiment verification.", "doi": "10.1111/jdi.70026", "pmid": "40470717", "authors": ["Shahad W Kattan", "Ahmed M Basri", "Mohammad H Alhashmi", "Amany I Almars", "Reem Hasaballah Alhasani", "Ifat Alsharif", "Ikhlas A Sindi", "Ahmad H Mufti", "Iman S Abumansour", "Nasser A Elhawary", "Aishah Abdullah Qahtani", "Hailah M Almohaimeed"], "journal": "Journal of diabetes investigation", "year": 2025, "abstract": "OBJECTIVE: Diabetes is a chronic disease resulting from insufficient insulin secretion or impaired insulin function. Diabetic nephropathy (DN) is one of the most common complications of diabetes and a leading cause of end-stage renal disease. Early diagnosis of DN is crucial for timely intervention and effective disease management.\nMETHODS: Gene expression profiles GSE142025 and GSE220226 were retrieved from the GEO database and combined into a metadata cohort, while GSE189007 was obtained as an independent validation dataset. Differentially expressed genes (DEGs) were identified in 46 glomerular samples from DN patients and 31 control samples. Gene Ontology (GO) and Disease Ontology (DO) enrichment analyses, gene set enrichment analysis (GSEA), least absolute shrinkage and selection operator (LASSO) regression, support vector machine-recursive feature elimination (SVM-RFE) analysis, and area under the curve (AUC) calculations were performed.\nRESULTS: A total of 109 DEGs were identified. Among them, DUSP1, EGR1, FPR1, G6PC, GDF15, LOX, LPL, PRKAR2B, PTGDS, and TPPP3 were selected as potential diagnostic biomarkers for DN. These biomarkers exhibited a positive correlation with immune cell infiltration. Experimental validation identified LOX as the most promising novel diagnostic biomarker for DN. 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