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DOI 10.1049/syb2.70081

Медицинская библиотека · IET systems biology · 2026

Identification of Mitochondria- and Macrophage Activation-Related Hub Genes in Sarcopenia.

Li Bangzhi, Shi Long, Wang Qiong, Li Yang, Zhao Liang, Zhao Rongcan, Wang Yanjin, Zhou Yingjie, Gu Shan

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Аннотация

To explore the hub genes and pathways associated with sarcopenia progression from the perspective of mitochondrial dysfunction and macrophage activation. The GEO datasets GSE8479, GSE1428 and GSE136344 were obtained from the GEO database. Mitochondria-related genes (MRGs) and macrophage activation-related genes (MARGs) were identified. Functional enrichment analyses, PPI analysis, diagnostic model construction, molecular subtyping and ssGSEA-based immune enrichment analysis were performed. Key genes were further validated by RT-qPCR. A total of 62 mitochondria- and macrophage activation-related differentially expressed genes (M&MARDEGs) were identified. Nine key genes (IGF1, FTL, MAPK8, MAPK9, TF, CREB1, FAS, VEGFA and NFKB1) were retained in the final diagnostic model. Immune enrichment analysis suggested distinct immune-related transcriptional characteristics among different risk groups and molecular subtypes. RT-qPCR validation demonstrated that IGF1, FAS and MAPK9 were significantly downregulated, whereas FTL, TF, CREB1 and NFKB1 were significantly upregulated in the sarcopenia model group. MAPK8 and VEGFA showed decreasing trends without statistical significance. Integrated transcriptomic analysis identified key genes potentially associated with sarcopenia through the intersection of mitochondrial dysfunction and macrophage activation. These findings provide insights into the molecular characteristics of sarcopenia and may offer candidate targets for future mechanistic and translational studies.

Для цитирования: Li Bangzhi, Shi Long, Wang Qiong, Li Yang, Zhao Liang, Zhao Rongcan, Wang Yanjin, Zhou Yingjie, Gu Shan. Identification of Mitochondria- and Macrophage Activation-Related Hub Genes in Sarcopenia.. IET systems biology. 2026. DOI: 10.1049/syb2.70081.

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