Evaluation of Sphingolipid Metabolism in Silicosis Patients.

OBJECTIVE

Silicosis is a fibrotic lung disease caused by the inhalation of crystalline silica. This study investigates sphingolipid metabolism in silicosis patients using plasma samples.

METHODS

GC-MS-based untargeted metabolomics identified alterations in the sphingolipid pathway, while LC-MS targeted specific ceramide and sphingomyelin species. Enzyme activities of acid ceramidase, neutral sphingomyelinase, sphingosine kinase-1, and sphingosine-1-phosphate lyase-1 were also assessed.

RESULTS

Results showed elevated sphingolipid levels and reduced enzyme activities in patients versus controls. In silico molecular docking suggested interactions between SiO 2 and pathway enzymes. Metabolomic analysis revealed disrupted sphingolipid and fatty acid pathways.

CONCLUSIONS

These findings highlight the role of sphingolipid dysregulation in silicosis pathogenesis and suggest its potential as a biomarker and therapeutic target. Understanding these mechanisms could improve management and treatment strategies for this debilitating disease.