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Table 4 Diagnostic performance of five non-invasive tests for determining significant steatosis (> 33% of hepatocytes)

From: Novel serum biomarkers modified by the body mass index z-score for the detection of liver fibrosis and steatosis in children with chronic hepatitis C

Significant steatosis (> 33% of hepatocytes)

Test

APRI

M-APRI

FIB-4

M-FIB-4

B-AST

AUROC (95% CI)

0.837 (0.657–0.945)

0.923 (0.820–0.999)

0.683 (0.488–0.840)

0.942 (0.792–0.994)

0.942 (0.792–0.994)

Cut-off

0.656

0.577

0.216

0.179

92.82

Sensitivity (95% CI)

75 (19.4–99.4)

100 (39.8–100)

75 (19.4–99.4)

100 (39.8–100)

100 (39.8–100)

Specificity (95% CI)

88.46 (69.8–97.6)

92.3 (74.9–99.1)

73.1 (52.2–88.4)

88.46 (69.8–97.6)

92.3 (74.9–99.1)

+ PV

50.0 (23.1–76.9)

66.7 (34.6–88.3)

30.0 (15.5–50.0)

57.1 (31.5–79.4)

66.7 (34.6–88.3)

- PV

95.8 (80.7–99.2)

100

95.0 (77.4–99.1)

100

100

  1. APRI aspartate-to-platelet ratio index, FIB-4 Fibrosis-4 index, M-APRI modified aspartate-to-platelet ratio index (BMI z-score x APRI), M-FIB-4 modified Fibrosis-4 index (BMI z-score x FIB-4), B-AST BMI z-score x AST, AUROC area under the receiver operating characteristic, 95% CI 95% confidence interval, + PV positive predictive value, − PV negative predictive value