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. Author manuscript; available in PMC: 2011 Sep 1.
Published in final edited form as: J Chem Neuroanat. 2010 Mar 27;40(1):63–70. doi: 10.1016/j.jchemneu.2010.03.005

Table 1.

Clinical, demographic, and neuropathological characteristics by diagnosis category

Clinical Diagnosis
Comparison by diagnosis group
NCI (N=10) MCI (N=10) AD (N=10) Total (N=30)
Age at death (years): Mean ± SD (Range) 82.3 ± 4.5 (76–90) 84.1 ± 5.7 (72–92) 90.2 ± 7.3 (80–101) 85.5 ± 6.7 (72–101) p = 0.05a
Number (%) of males: 5 (50%) 4 (40%) 3 (30%) 12 (40%) p = 0.9b
Years of education: Mean ± SD (Range) 19.4 ± 3.2 (15–25) 20.0 ± 2.1 (17–24) 17.9 ± 2.6 (14–22) 19.1 ± 2.7 (14–25) p = 0.2a
Number (%) with ApoE ε4 allele: 0 0 4 (40%) 4 (13%) p = 0.5b
MMSE: Mean ± SD (Range) 28.2 ± 1.0 (27–30) 28.1 ± 1.8 (25–30) 16.4 ± 5.8 (7–24) 24.2 ± 6.6 (7–30) p < 0.0001a*
Global Cognitive Score (GCS): Mean ± SD (Range) 0.71 ± 0.24 (0.37–1.20) 0.39 ± 0.32 (−0.17, 0.83) −0.81 ± 0.52 (−1.52, −0.16) 0.13 ± 0.75 (−1.52, 1.20) p < 0.0001a*
Postmortem interval (hours): Mean ± SD (Range) 5.1 ± 3.0 (2.3–12.4) 4.7 ± 2.4 (2.7–10.0) 6.1 ± 3.5 (2.7–12.4) 5.3 ± 2.9 (2.3–12.4) p = 0.7a
Distribution of Braak scores: I-II 4 5 0 9 p = 0.0003a*
III-IV 6 5 4 15
V-VI 0 0 6 6
Distribution of NIA Reagan diagnosis (likelihood of AD): No AD 0 0 0 0 p = 0.0005a*
Low 5 7 0 12
Intermediate 5 3 5 13
High 0 0 5 5
a

Kruskal-Wallis test.

b

Fisher's exact test.

*

Pairwise comparisons with Bonferroni correction showed that there was no significant difference between NCI and MCI, but both were significantly different from AD (p<0.01).