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. 2021 Mar 8;80(4):325–335. doi: 10.1093/jnen/nlab017

TABLE 1.

Clinical, Demographic, and Neuropathological Characteristics by Diagnosis Category

Diagnosis
p value Pair-wise comparison
NC-LP (n = 8) NC-HP (n = 7) MCI (n = 7) AD (n = 7)
Age (years) at death:
 Mean ± SD (range) 85.8 ± 5.2 (72–90) 89.1 ± 6.2 (84–100) 87.1 ± 3.8 (44–95) 81.7 ± 9.1 (69–93) 0.2*
Number (%) of males: 5 (63%) 3 (43%) 3 (43%) 5 (71%) 0.6
Years of education:
 Mean ± SD (range) 16.0 ± 2.6 (12–20) 16.1 ± 0.9 (15–18) 17.1 ± 1.1 (16–18) 16.0 ± 2.3 (12–20) 0.9*
Number (%) with ApoE ε4 allele 1 (13%) 1 (14%) 3 (43%) 4 (57%) 0.06
Number (%) with hypertension 5 (63%) 4 (57%) 4 (57%) 4 (57%) 1.0
MMSE
 Mean ± SD (range) 29.1 ± 0.8 (28–30) 28.9 ± 1.5 (26–30) 26.0 ± 1.9 (23–28) 19.4 ± 4.1 (11–25) 0.0001* (NC-LP, NC-HP) > AD
Postmortem interval (hours)
 Mean ± SD (range) 3.8 ± 2.6 (1.8–10.0) 3.8 ± 3.2 (1.3–10.8) 3.4 ± 1.4 (1.2–6.0) 4.4 ± 2.1 (2.7–8.5) 0.6*
Identified microinfarcts
 Mean ± SD (range) 0.2 ± 0.4 (0–1) 0.6 ± 0.8 (0–2) 0.6 ± 0.8 (0–7) 0.7 ± 1.0 (0–2) 0.1*
Distribution of Braak scores:
 0 2 0 0 0
 I/II 6 0 3 1 0.0005* NC-LP < (NC-HP, AD)
 III/IV 0 7 4 3
 V/VI 0 0 0 3
NIA Reagan diagnosis(likelihood of AD)  
 No AD 2 1 1 0
 Low 5 1 3 1 0.02* NC-LP < AD
 Intermediate 1 5 3 3
 High 0 0 0 3
CERAD diagnosis
 No AD 4 1 2 0
 Possible 1 1 2 0 0.07*
 Probable 2 3 3 5
 Definite 1 2 0 2

AD, Alzheimer disease; CERAD, Consortium to Establish a Registry for Alzheimer disease; MCI, mild cognitive impairment; NC-LP, normal cognition-low AD pathology; NC-HP, normal cognition-high AD pathology.

*

Kruskal-Wallis test, with Dunn’s test for multiple comparisons.

Fisher exact test, with Bonferroni correction for multiple comparisons.