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. Author manuscript; available in PMC: 2024 Sep 17.
Published in final edited form as: J Alzheimers Dis. 2023;96(2):563–578. doi: 10.3233/JAD-230223

TABLE 1.

Clinical and postmortem characteristics of the analytic cohort

Variable No Dementia
n=175
Dementia*
n=125
mean or n SD or % mean or n SD or %
Age at study baseline 82.17 5.81 82.77 5.39
Age at death 90.73 6.08 91.27 6.27
Years of education 14.94 2.91 14.55 3.12
Female sex n=123 70% n=90 72%
History of head injury n=73 42% n=46 37%
Number of illnesses last visit (0,7) 0.61 0.92 0.36 0.59
APOE4 genotype n=25 14% n=49 39%^
Final cognitive status no cognitive impairment n=107 61% - -
Final cognitive status mild cognitive impairment n=68 39% - -
Global cognition at baseline 0.17 0.51 −0.50 0.81^
Global cognition at last visit −0.17 0.58 −2.16 0.92^
Minimental Status Exam at baseline (0-30) 28.0 1.68 25.12 5.53^
Minimental Status Exam at last visit (0-30) 26.7 2.57 11.29 8.42^
Time from last cognitive exam to death (months)** 9.6 6.5,14.0 6.2 3.8,10.1^
Postmortem interval (hours) 9.64 9.28 8.75 4.57
# Tau-tangles density 5.15 5.08 14.50 12.19^
# Aβ burden 3.75 3.79 5.40 3.79^
Global AD pathology score 0.62 0.54 1.09 0.67^
CERAD (Yes, definite/probable) n=107 61% n=109 87%^
ADNC (pathologic diagnosis of AD) n=104 50% n=103 82%^
*

t-test or Chi-square significance <0.001

**

median, interquartile range (IQR)

#

Aβ and tau-tangles indices collected from 8 sites within the cerebrum as described in the methods