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. Author manuscript; available in PMC: 2019 Mar 1.
Published in final edited form as: J Neurochem. 2017 Nov 6;144(5):634–643. doi: 10.1111/jnc.14218

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.)