Immunological profile of lactate metabolism-related genes in Psoriasis a comprehensive analysis based on bulk and single-cell RNA sequencing data

Psoriasis (Pso) is a chronic erythema squamous disease often accompanied by metabolic abnormalities. Disturbances in lactate metabolism have been observed in the skin of patients with Pso, but the role of lactate metabolism in the pathogenesis of Pso remains unclear. To identify core genes associated with lactate metabolism in Pso, we downloaded and merged two Pso-related datasets (GSE13355, GSE109248) from the GEO database. Through comprehensive analysis, we analyzed the functions associated with these hub genes and the correlation between their expression levels and immune infiltration. Additionally, we explored lactate metabolism-related hub genes in different immune cells using single-cell sequencing data. We identified four lactate metabolism-related hub genes that are highly associated with Pso. Further analysis revealed that these four hub genes were significantly correlated with the levels of immune cell infiltration. To further elucidate the impact of lactate metabolism on immune cells, we analyzed single-cell sequencing data from healthy controls and Pso patients. The expression of lactate metabolism-related hub genes was primarily observed in moDCs and T cells. These results suggest that lactate metabolism-related genes and their functions are closely associated with changes in inflammatory cells in Pso patients. This study provides new insights into the role of lactate metabolism in the pathogenesis of Pso and highlights potential therapeutic targets for the disease.

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Publication Details

Journal
Scientific Reports
Published
2025-02-26
DOI
https://doi.org/10.1038/s41598-025-91237-z
Citations
1
Primary Topic
Psoriasis: Treatment and Pathogenesis
Type
article
Field-Weighted Citation Impact
0.80
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Immunological profile of lactate metabolism-related genes in Psoriasis a comprehensive analysis based on bulk and single-cell RNA sequencing data

F. Li, Juan Lv, Siyu Liu, Yixuan Zhang
1 citations
Scientific Reports
Psoriasis: Treatment and Pathogenesis
0.80
article

Immunological profile of lactate metabolism-related genes in Psoriasis a comprehensive analysis based on bulk and single-cell RNA sequencing data

F. Li, Juan Lv, Siyu Liu, Yixuan Zhang
article en
1 citations

Abstract

Psoriasis (Pso) is a chronic erythema squamous disease often accompanied by metabolic abnormalities. Disturbances in lactate metabolism have been observed in the skin of patients with Pso, but the role of lactate metabolism in the pathogenesis of Pso remains unclear. To identify core genes associated with lactate metabolism in Pso, we downloaded and merged two Pso-related datasets (GSE13355, GSE109248) from the GEO database. Through comprehensive analysis, we analyzed the functions associated with these hub genes and the correlation between their expression levels and immune infiltration. Additionally, we explored lactate metabolism-related hub genes in different immune cells using single-cell sequencing data. We identified four lactate metabolism-related hub genes that are highly associated with Pso. Further analysis revealed that these four hub genes were significantly correlated with the levels of immune cell infiltration. To further elucidate the impact of lactate metabolism on immune cells, we analyzed single-cell sequencing data from healthy controls and Pso patients. The expression of lactate metabolism-related hub genes was primarily observed in moDCs and T cells. These results suggest that lactate metabolism-related genes and their functions are closely associated with changes in inflammatory cells in Pso patients. This study provides new insights into the role of lactate metabolism in the pathogenesis of Pso and highlights potential therapeutic targets for the disease.

Scientific ReportsVol. 15(1)
Zhejiang Chinese Medical University (CN), Guangzhou University of Chinese Medicine (CN), Jiangmen Wuyi Traditional Chinese Medicine Hospital (CN)
Zero hunger
Openalex Percentile: Top 31%
Psoriasis: Treatment and Pathogenesis
0.80
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