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. Author manuscript; available in PMC: 2021 Dec 1.
Published in final edited form as: Neuropathol Appl Neurobiol. 2021 May 21;47(7):1050–1059. doi: 10.1111/nan.12727

Table 1.

Demographic and clinical characteristics of the three study groups

Characteristic No. or median (% or interquartile range)
gFTLD-TDP (n=15) AD-TDP (n=10) Pure-TDP (n=10) p-value
Female 6 (40%) 5 (50%) 4 (40%) 0.91
White/Caucasian 14 (93%) 10 (100%) 10 (100%) >0.99
Age at onset, years 68 (66 – 70) 69 (67 – 75) 73 (67 – 77) 0.20
Disease duration, years 10 (9 – 15) 11 (10 – 18) 9 (5 – 14) 0.27
Age at death, years 79 (76 – 84) 83 (78 – 87) 78 (77 – 87) 0.24
Family history 10 (67%) 8 (80%) 4 (40%) 0.18
Education, years 15 (12 – 16) 16 (12 – 17) 16 (14 – 17) 0.67
Last MMSE/30 13 (5 – 25) 17 (5 – 22) 16 (2 – 22) 0.85a
Clinical diagnosis
FTLD clinical spectrum diagnosis 5 (33%) 3 (30%) 3 (30%)
Frontotemporal dementia (FTD) 2 (13%) 0 (0%) 0 (0%) 0.75
FTD-Motor Neuron Disease 0 (0%) 0 (0%) 1 (10%)
Primary progressive aphasia 2 (13%) 1 (10%) 1 (10%)
Progressive supranuclear palsy 1 (7%) 0 (0%) 1 (10%)
Corticobasal syndrome 0 (0%) 2 (20%) 0 (0%)
Alzheimer’s dementia 8 (53%) 7 (70%) 5 (50%)
Dementia with Lewy bodies 1 (7%) 0 (0%) 1 (10%)
Vascular dementiab 1 (7%) 0 (0%) 1 (10%)

Data are represented as median (interquartile range) for continuous variables or number (per cent) for categorical variables. P-values are from Kruskal-Wallis test for continuous variables or Fisher’s exact test for categorical variables

a

Adjusted for disease duration at the time of last MMSE

b

No or minimal evidence (vascular score 0/1) of cerebrovascular disease on brain autopsy in both cases