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. Author manuscript; available in PMC: 2015 Aug 1.
Published in final edited form as: Neurobiol Aging. 2015 Apr 25;36(8):2340–2347. doi: 10.1016/j.neurobiolaging.2015.04.011

TABLE 1.

Demographic and clinical characteristics according to AD phenotype

EOAD PCA lvPPA LOAD
N 53 52 29 42
Age 61.5±4.4 62.6±7.6 67.0±7.7a 75.8±3.0b
Sex (% male) 55.2 58.5 59.5 51.9
Education* 5.3±1.0 5.0±1.1 4.7±1.5 4.9±1.3
MMSE 21.5±5.4 22.2±3.4 21.8±4.3 22.1±3.9
CDR 0.7±0.3 0.8±0.2 0.9±0.2 0.8±0.2
TIV (L) 1.56±0.13 1.57±0.14 1.61±0.14 1.57±0.14
CSF Aβ42(ng/L)** 480±90 459±98 469±117 433±103
CSF Total tau (ng/L) 695±358 728±309 788±376 785±336
% CSF total tau >375 84.9 92.3 85.7 90.5
CSF Phospho tau (ng/L) 92±40 93±38 96±34 97±39
% CSF phospho tau >52 79.2 90.4 93.1 90.5

Abbreviations: PCA = Posterior cortical atrophy; lvPPA = Logopenic variant primary progressive aphasia; EOAD = Early-onset Alzheimer’s disease; LOAD = Late-onset Alzheimer’s disease; MMSE = Mini-mental state examination; CDR = Clinical dementia rating scale; TIV = Total intracranial volume.

Data are presented as mean ± SD unless otherwise stated. Differences between groups were analyzed using ANOVA with post-hoc Bonferroni tests (age, MMSE, CDR, TIV, CSF), X2 tests (sex), Kruskal-Wallis with post-hoc Mann-Whitney U-tests (education) and bootstrapping (% of suprathreshold CSF concentrations).

*

using Verhage’s classification (scale 1–7(Verhage, 1964)),

**

Only patients with CSF Aβ42 <640 were included,

a

lvPPA > PCA & EOAD, p<0.01;

b

LOAD > all other groups, p<0.001.