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pmid:40822282

Research on the diagnosis model of osteoarthritis based on methylation-related genes using machine learning algorithms.

Xu Cui · Houlin Ji · Shengyang Guo · Ju Liu · Linyuan Zhang · Yongwei Jia · Yin Cui · Xiaoxiao Zhou

Frontiers in genetics · 2025 doi:10.3389/fgene.2025.1595676

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
Research on the diagnosis model of osteoarthritis based on methylation-related genes using machine learning algorithms.
doi
10.3389/fgene.2025.1595676
pmid
40822282
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Xu Cui
[1]
Houlin Ji
[2]
Shengyang Guo
[3]
Ju Liu
[4]
Linyuan Zhang
[5]
Yongwei Jia
[6]
Yin Cui
[7]
Xiaoxiao Zhou
journal
Frontiers in genetics
year
2025
abstract
Objective: To construct a diagnostic model of osteoarthritis related to methylation genes using machine learning algorithms, and analyze its prognostic value and biological functions. Methods: The GSE 63695 and GSE162484 datasets including human osteoarthritis (OA) and normal samples were downloaded from the GEO datasets. The microarray chip data of chondrocytes were analyzed using R software to obtain differentially methylated genes. Genes were selected through SVM-RFE analysis and LASSO regression model, and a diagnostic model for OA was established. The performance of the model was assessed by the receiver operating characteristic (ROC) curve. The gene set enrichment analysis of Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) was carried out on the genes incorporated within the model. Results: An overall 11 DEGs were identified:7 genes were remarkably upregulated and 4 genes were distinctly downregulated. By means of machine learning algorithms, ARHGEF10, ATP11A, NOTCH1, THSD4, NIPA1, SIM2, MAN1C1, ENDOG, CCNC, TAF5, and VPS52 were ultimately incorporated into the model, which could effectively diagnose OA. The area under the curve (AUC) in the datasets GSE 63695 and GSE162484 was 0.96 and 0.93 respectively. Conclusion: The diagnostic model of methylation-related genes constructed based on machine learning algorithms can effectively identify OA.
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A machine-learning diagnostic model based on 11 methylation-related genes achieved AUCs of 0.96 and 0.93 in GSE 63695 and GSE162484, respectively.
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The area under the curve (AUC) in the datasets GSE 63695 and GSE162484 was 0.96 and 0.93 respectively.
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A machine-learning diagnostic model based on 11 methylation-related genes achieved AUCs of 0.96 and 0.93 in GSE 63695 and GSE162484, respectively.
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Genome-Wide Differentially Methylated Region Analysis to Reveal Epigenetic Differences of Articular Cartilage in Kashin-Beck Disease and Osteoarthritis
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Characterization of the cartilage DNA methylome in knee and hip osteoarthritis.
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The microarray chip data of chondrocytes were analyzed using R software to obtain differentially methylated genes. Genes were selected through SVM-RFE analysis and LASSO regression model, and a diagnostic model for OA was established. The performance of the model was assessed by the receiver operating characteristic (ROC) curve. The gene set enrichment analysis of Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) was carried out on the genes incorporated within the model.\nResults: An overall 11 DEGs were identified:7 genes were remarkably upregulated and 4 genes were distinctly downregulated. By means of machine learning algorithms, ARHGEF10, ATP11A, NOTCH1, THSD4, NIPA1, SIM2, MAN1C1, ENDOG, CCNC, TAF5, and VPS52 were ultimately incorporated into the model, which could effectively diagnose OA. 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