Review Article
Sepsis-Induced Brain Dysfunction: Pathogenesis, Diagnosis, and Treatment
Table 1
Suggested biomarkers to monitor sepsis-induced brain dysfunction.
| Biomarkers | Significance | Location |
| C-reactive protein (CRP) and Procalcitonin (PCT) | Higher CRP levels indicated prolonged acute brain dysfunction [149] | Plasma | C-type natriuretic peptide (NT-proCNP) | High-peak concentration of NT-proCNP in the early phase of sepsis could predict SAE [150] | Plasma | IL-6, IL-8, IL-10, TNF-α and S-100β | Negatively associated with delirium free days [151] | Plasma | Neurofilament (Nf) | Nf could predict poorer cognitive outcome in SAE patients [151] | Cerebrospinal fluid (CSF) and plasma | Adiponectin, Tau, and neopterin | Significantly higher in patients with delirium [152] | Plasma |
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