Table 3. C-statistic for the base clinical model and incremental change with addition of novel biomarkers in the full study sample and intermediate risk population.
Model | Full study sample | Intermediate risk¶ |
---|---|---|
Base clinical model | 0.890 | 0.764 |
Base clinical model + log(KIM-1/Cr) | 0.890 | 0.774 |
Base clinical model + log(KIM-1) | 0.891 | 0.779 |
Base clinical model + log(NGAL/Cr) | 0.890 | 0.766 |
Base clinical model + log(NGAL) | 0.891 | 0.762 |
Base clinical model + log(NAG/Cr) | 0.890 | 0.768 |
Base clinical model + log(NAG) | 0.890 | 0.775 |
Base clinical model + L-FABP/Cr* | 0.890 | 0.762 |
Base clinical model + L-FABP** | 0.890 | 0.766 |
L-FABP/Cr was divided in to those with undetectable levels, those with absolute levels below the lower limit of detection, and then into tertiles of the normalized biomarker
LFABP was divided in to those with undetectable levels, those with absolute levels below the lower limit of detection, and then into tertiles of the raw biomarker
Intermediate risk population had eGFR ≥60 ml/min/1.73m2 and ACR ≥30 mg/g Cr; or eGFR 45–59 ml/min/1.73m2 and ACR 0–300 mg/g Cr; or eGFR 30–44 ml/min/1.73m2 and ACR <30 mg/g Cr