Table 3.
Characteristics | Normal (n = 50) vs. Prodromal AD (n = 23) groups | Normal (n = 50) vs. AD dementia (n = 28) groups | ||||||||
---|---|---|---|---|---|---|---|---|---|---|
Cut-off | Sen (%) | Spe (%) | AUC | p value | Cut-off | Sen (%) | Spe (%) | AUC | p value | |
Plasma factors | ||||||||||
FXIIa activity, U/ml | > 26.3 | 73.9 | 74.0 | 0.783 | < 0.001 | > 27.2 | 78.6 | 78.0 | 0.906 | < 0.001 |
FXIa activity, U/ml | > 1.13 | 52.2 | 52.0 | 0.566 | 0.367 | > 1.17 | 57.1 | 58.0 | 0.659 | 0.020 |
FXa activity, U/ml | > 0.76 | 56.5 | 54.0 | 0.573 | 0.316 | > 0.82 | 71.4 | 70.0 | 0.779 | < 0.001 |
Kallikrein activity, U/ml | > 1.21 | 56.5 | 56.0 | 0.609 | 0.138 | > 1.29 | 64.3 | 64.0 | 0.772 | < 0.001 |
CSF biomarkers | ||||||||||
Aβ1–42 levels, pg/ml | < 832.4 | 87.0 | 88.0 | 0.962 | < 0.001 | < 721.7 | 89.3 | 98.0 | 0.979 | < 0.001 |
t-Tau levels, pg/ml | > 252.6 | 65.2 | 66.0 | 0.701 | 0.006 | > 315.3 | 85.7 | 86.0 | 0.954 | < 0.001 |
p-Tau181 levels, pg/ml | > 46.1 | 65.2 | 64.0 | 0.690 | 0.009 | > 46.1 | 78.6 | 78.0 | 0.870 | < 0.001 |
BK levels, pg/ml | > 46.1 | 54.5 | 56.5 | 0.656 | 0.073 | > 52.8 | 74.1 | 73.9 | 0.783 | 0.001 |
Ratios | ||||||||||
Aβ1–42 / FXIIa | < 33.8 | 87.0 | 86.0 | 0.965 | < 0.001 | < 27.4 | 100.0 | 100.0 | 1.000 | < 0.001 |
Aβ1–42 / FXIa | < 742.5 | 82.6 | 82.0 | 0.930 | < 0.001 | < 635.4 | 96.4 | 96.0 | 0.993 | < 0.001 |
Aβ1–42 / FXa | < 1,091 | 82.6 | 82.0 | 0.933 | < 0.001 | < 941.8 | 96.4 | 96.0 | 0.994 | < 0.001 |
Aβ1–42 / Kallikrein | < 680.9 | 87.0 | 86.0 | 0.943 | < 0.001 | < 584.8 | 96.4 | 96.0 | 0.994 | < 0.001 |
Statistically-derived optimal cut-off value was determined with the best balance between sensitivity (Sen) and specificity (Spe) values. Discrimination of prodromal AD and AD dementia from normal group was evaluated by receiver operator characteristics (ROC) curve analysis and quantified by the area under the curve (AUC) using SPSS software version 24.0