Table 3:

Comparative diagnostic accuracy of investigated parameters differentiating glioma gradesa

Models and ParametersAUC95% CIOptimal CutoffSensitivity (%)Specificity (%)P Value
Nondiffusion
 Enhancementb0.760.65–0.870.5 ↑81.470.2<.001
 Necrosisb0.810.71–0.910.5 ↑67.494.6<.001
 T2LFMb0.580.46–0.710.5 ↓16.2100.006
 Hemorrhageb0.730.61–0.840.5 ↑51.294.6<.001
ADC
 ADCc0.880.80–0.961.217 ↓75.788.4<.001
DTI
 FA0.640.52–0.770.174 ↑46.586.5.01
 MDc0.880.80–0.951.134 ↓83.876.7<.001
DKI
 AK0.930.87–1.000.494 ↑97.775.7<.001
 RK0.930.88–1.000.627 ↑83.791.9<.001
 MK0.930.88–1.000.539 ↑93.081.1<.001
 KFA0.530.40–0.670.219 ↓78.444.2.85
 MKT0.940.88–0.990.564 ↑88.486.5<.001
SMT
 LMDc0.660.53–0.792.967 ↓83.855.8<.001
 TMDc0.910.84–0.972.958 ↓91.979.1<.001
 µFA0.940.88–0.990.509 ↑90.786.5<.001
 µFA30.940.88–0.990.132 ↑90.786.5<.001
 MMDc0.900.83–0.971.311 ↓89.276.7<.001
 INVF0.940.88–0.990.319 ↑90.786.5<.001
 IDc0.770.67–0.881.946 ↓83.865.1<.001
 ETMDc0.820.72–0.911.208 ↓94.660.5<.001
 EMMDc0.720.60–0.841.502 ↓75.767.4<.001
  • Note:—T2LFM indicates T2 FLAIR mismatch; FA, fractional anisotropy; MD, mean diffusivity; KFA, kurtosis fractional anisotropy; LMD, longitudinal microscopic diffusivity; µFA3, microscopic fractional anisotropy to the third power; MMD, microscopic mean diffusivity; ID, intrinsic diffusivity; ETMD, extraneurite transverse microscopic diffusivity; EMMD, extraneurite microscopic mean diffusivity.

  • a Optimal cutoff levels to predict glioma grade (low-grade versus high-grade) were assessed by the Youden index. Cutoffs were evaluated by sensitivity and specificity. An upward arrow (↑) indicates a positive correlation, in which values above the cutoff point predict a high-grade glioma, whereas a downward arrow (↓) indicates a negative correlation, in which values below the cutoff point predict a high-grade glioma. P values were computed by comparing the AUC against chance performance.

  • b Binary variable, indicating the presence or absence of the feature.

  • c Units mm2/s × 10−3.