AI Article Synopsis

  • Emerging research links the development of carotid atherosclerosis to immune system activation and inflammation, revealing that the exact immune pathways involved are still not fully understood.
  • The study analyzed gene expression data to identify 178 differentially expressed genes, ultimately highlighting five key genes that may serve as biomarkers for advanced carotid atherosclerotic plaques.
  • Findings emphasize the important role of immune cells, such as macrophages and T cells, in plaque development, suggesting that these immune-related genes could lead to new treatment strategies for atherosclerosis in a predictive and personalized manner.

Article Abstract

Emerging evidence shows that carotid atherosclerosis is related to the activation of immune-related pathways and inflammatory cell infiltration. However, the immune-linked pathways that helped in the advancement of the carotid atherosclerotic plaque and the association of such plaques with the infiltration status of the body's immune cells still unclear. Here, the expression profiles of the genes expressed during the progression of the carotid atherosclerotic plaques were retrieved from the Gene Expression Omnibus database and 178 differentially expressed genes were examined. The Weighted Gene Coexpression Network Analysis technique identified one of the brown modules showed the greatest correlation with carotid atherosclerotic plaques. In total, 66 intersecting genes could be detected after combining the DEGs. LASSO regression analysis was subsequently performed to obtain five hub genes as potential biomarkers for carotid atherosclerotic plaques. The functional analysis emphasized the vital roles played by the inflammation- and immune system-related pathways in this disease. The immune cell infiltration results highlighted the significant correlation among the CD4+ T cells, B cells, macrophages, and CD8+ T cells. Thereafter, the gene expression levels and the diagnostic values related to every hub gene were further validated. The above results indicated that macrophages, B cells, CD4+ T cells, and CD8 + T cells were closely related to the formation of the advanced-stage carotid atherosclerotic plaques. Based on the results, it could be hypothesized that the expression of hub genes (C3AR1, SLAMF8, TMEM176A, FERMT3, and GIMAP4) assisted in the advancement of the early-stage to advanced-stage carotid atherosclerotic plaque through immune-related signaling pathways. This may help to provide novel strategies for the treatment of carotid plaque in the context of predictive, preventive, and personalized medicine.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596267PMC
http://dx.doi.org/10.1155/2022/7657379DOI Listing

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