Skip to main content
. Author manuscript; available in PMC: 2022 Nov 29.
Published in final edited form as: Neurobiol Aging. 2022 Jul 5;118:88–98. doi: 10.1016/j.neurobiolaging.2022.06.013

Table 1.

VMAP Cohort Demographics

Characteristic Clinical Diagnosis Total
(N=155)
P-value
Normal Cognition
(N=83)
Mild Cognitive
Impairment (N=72)
Male, no. (%) 58 (70) 46 (63) 104 (67) 0.535
Age (baseline) 72±6.50 72±6.18 72±6.33 0.458
Education 17±2.41 15±2.94 16±2.80 0.001
APOE-ε4 carriers, no. (%) 24 (29) 27 (38) 51 (33) 0.334
sTREM2 CSF pg/mL 3530±1867.29 3817±1759.49 3667±1812.50 0.327
p-tau181 CSF pg/mL (% p-tau positive) 56±21.92(17) 67±28.59(26) 61±25.70(21) 0.212
1-42 CSF pg/mL (% Aβ positive) †† 760±229.54 (20) 662±254.02 (40) 714±245.40 (30) 0.012

Values are presented as mean±standard deviation, unless otherwise indicated. A student’s t-test or a Pearson’s chi-squared test was used to compare continuous or categorical variables, respectively, between cognitive diagnoses. Bold represents statistical significance set to a priori threshold P<0.05. 6 participants are Black/African American; 2 American Indian/Alaska Native; 2 Asian.

p-tau positive ≥ 80pg/mL

††

Aβ positive ≤ 530pg/mL.