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editorial
. 2008 Sep 22;23(12):3737–3743. doi: 10.1093/ndt/gfn531

Table 1.

NGAL as an AKI biomarker

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.