Опубликована: Авг. 23, 2024
Язык: Английский
Опубликована: Авг. 23, 2024
Язык: Английский
Frontiers in Aging Neuroscience, Год журнала: 2025, Номер 17
Опубликована: Март 26, 2025
Background Alzheimer’s disease (AD) is a typical neurodegenerative that presents challenges due to the lack of biomarkers identify AD. A growing body evidence highlights critical role circadian rhythms in Methods The differentially expressed clock genes (DECGs) were identified between AD and ND groups (non-demented controls). Functional enrichment analysis was executed on DECGs. Candidate diagnostic for screened by machine learning. ROC nomograms constructed evaluate candidate biomarkers. In addition, therapeutics targeting predictive through DGIdb website. Finally, mRNA–miRNA network constructed. Results Nine DECG groups. Enrichment nine indicated pathways enriched long-term potentiation entrainment. Four (GSTM3, ERC2, PRKCG, HLA-DMA) using Lasso regression, random forest, SVM, GMM. performance four evaluated curve. Furthermore, nomogram HLA-DMA are good diagnosing Single-gene GSEA main oxidative phosphorylation, neurodegeneration-multiple diseases, etc. results immune cell infiltration there significant differences 15 subsets Moreover, 23 drugs 8 PRKCG Conclusion We three associated with genes, thus providing promising therapeutic targets
Язык: Английский
Процитировано
0Опубликована: Авг. 23, 2024
Язык: Английский
Процитировано
0