TABLE 2.
Components of the scoring system used to select patients most likely to have SIVD-BD
Features used in scale scores | BDS | PCA/EFA |
---|---|---|
I. Clinical features (4 points if present)* | ||
1. Hypertension (HTN) | X | |
2. Diabetes mellitus (DM) | X | |
3. Hyper-reflexia (REF) | X | |
4. Imbalance (GAIT) | X | |
II. Neuropsychological testing (1 point) | ||
5. Executive <45 (Exec T score)† | X | X |
III. Metabolites in WM (1H-MRSI) (1 point) | ||
6. N-acetylaspartate (NAA)<1212 | X | X |
7. Choline (CHO) | X | |
8. Creatine and phosphocreatine (CR) | X | |
IV. Inflammation and BBB (3 points) | ||
9. Albumin index >6.0 (albumin ratio) | X | X |
10. BBB permeability Ki >0.001813 | X | X |
11. MMP-2 index <0.0118 | X | X |
12. MMP-9 index | X | |
V. Alzheimer’s biomarkers (1 point) | ||
13. Aβ42/log(P-τ181) >150 | X | X |
Two scales were shown: (1) a 10-point Binswanger Disease Score (BDS) with one point for each feature; and (2) the Principal Component Analysis/Exploratory Factor Analysis (PCA/EFA).
Points are used in calculation of the BDS with score of 6 or greater suggestive of BD.
Cut-off determined from control sample.
Aβ42, amyloid-β1–42; BBB, blood-brain barrier; BD, Binswanger disease; BDS, Binswanger disease score; EFA, exploratory factor analysis; 1H-MRSI, proton MR spectroscopic imaging; MMP, matrix metalloproteinase; P-τ181, phosphorylated-τ181; PCA, principal component analysis; WM, white matter. (See (Rosenberg et al. 2015) for discussion of use of BDS and EFA.)