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ABSTRACT: Background
Neonatal sepsis (NS) is a systemic inflammatory response to severe pathogenic infections, and is a major cause of high morbidity and mortality in newborns. Currently, there is a lack of efficient diagnostic technology to accurately and rapidly diagnose NS, and the precise pathogenesis of NS has yet to be fully elucidated. The present study aimed to identify the optimal biomarkers in the progression of NS.Methods
The differentially expressed genes (DEGs) between NS and controls in the discovery datasets were screened. Gene set variation analysis (GSVA) was used to enrich the changes in biological functions and pathways in sepsis patients compared to healthy individuals. The differences in immune cell infiltration between these two groups were assessed using CIBERS
SUBMITTER: Yan R
PROVIDER: S-EPMC9674918 | biostudies-literature | 2022 Nov
REPOSITORIES: biostudies-literature