Table 5

Summary of univariate and multivariate logistical models and diagnostic accuracy of identifying NCD*

Serum biomarkersMU1MU2MU3MU4MU5MM1
Intercept−4.11±1.96−2.61±0.96−4.90±2.84−1.41±0.39−2.60±1.030.02±0.31
S100A8/90.40±0.290.62±0.43
S100B0.41±0.281.69±1.16
NGAL0.78±0.57−0.94±0.68
aNR2-AB−0.81±0.523.35±1.11
aP-AB2.03±1.101.82±0.82
AUC (95% CI) in %69.0 (53.8 to 84.3)62.8 (46.0 to 79.7)56.5 (39.1 to 74.0)62.5 (47.9 to 77.0)70.3 (59.0 to 81.6)83.4 (73.3 to 93.5)
p Value†0.0230.0040.0010.0020.004Reference
Cut-off value‡S100A8/9>850S100B>30NGAL>240aNR2-AB<1aP-AB≥1>11§
Sensitivity (%)85.757.126.786.786.7100.0
Specificity (%)51.070.292.051.054.076
  • *A MU model uses one SBM as the single predictor in the logistical model and the MM1 uses all listed predictors in the model.

  • †p Value is used to compare AUCs between a MU model and MM1 model using non-parametric Mann-Whitney U tests.

  • ‡The cut-off is corresponded to a ‘best’ pair of sensitivity and specificity which the average is the largest among all possible pairs on the receiver operating characteristic curve.

  • §The value represents a cut-off of propensity score from the multivariate logistical model MM1. The propensity score in this model is calculated in two steps. In step 1, a raw score or r-score is calculated using the r-score=0.62×S100A8+15+1.7×S100B−0.9×NGAL +3.4×NR2+1.8×Ribosomal-P+0.8×Ds-DNA +0.02. In the next step, the r-score is converted into the propensity score or p-score using p-score=100×exp(r-score)/(1+exp(r-score)).

  • aP-AB, antiribosomal P antibodies; AUC, area under the receiver operating characteristic curve; NGAL, neutrophil gelatinase associated lipocalin; aNR2-AB, antibodies to NR2 glutamate receptor.