Table 1.
Biomarker property | NGAL |
---|---|
Specific to AKI (AKI versus CKD versus systemic disease) | +/−a |
Discern AKI sub-types (pre-renal azotemia versus intrinsic AKI) | Yes |
Sensitive to establish an early diagnosis | Yes |
Conserved across species | Yes |
High gradient to allow early and easy detection | Yes |
Proportional increase with injury or loss of function | Yes |
Associated with a known mechanism | Yes |
Results available while damage is limitable | Yes |
Results predict clinical outcomes | Yes |
Practical to measure | Yes |
Amendable to existing platform assay methods | Yes |
aPlasma NGAL may be detected in chronic kidney disease (CKD), chronic hypertension, systemic infections, inflammatory conditions and malignancies [51–56]. Urine NGAL may be detected in CKD, lupus nephritis and urinary tract infections [57–60]. In all these situations, NGAL values are generally substantially blunted compared to those typically measured in AKI.