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. 2020 Aug 24;143(9):2844–2857. doi: 10.1093/brain/awaa219

Table 1.

Cohort demographics from UPENN CNDR and UK-ADC

UPENN CNDR
UK-ADC
FTLD-TDP LATE-NC FTLD-TDP LATE-NC
n 33 30 8 14
Age at death (mean ± SD) 66.6 ± 9.3 88.6 ± 6.4 62.9 ± 9.8 90.9 ± 8.5
Clinical diagnosis at last exama
 No documented impairment 0 0 2 0
 Mild cognitive impairment 0 3 0 0
 Vascular dementia 0 1 0 2
 Probable Alzheimer’s disease 2 26 0 12
 bvFTD-FTLD 2 0 2 0
 bvFTD-FTLD/MND 5 0 2 0
 bvFTD-FTLD/PPA 5 0 2 0
Genetics
C9orf72 expansion 11 0 N/A N/A
GRN variant 7 0 N/A N/A
TBK1 variant 1 0 N/A N/A
VCP mutation 0 0 1 N/A
FTLD-TDP type
 Type A or B 23 N/A 4 N/A
 Type C 6 N/A 2 N/A
 Type D 0 N/A 1 N/A
 Type E 4 N/A 1 N/A
LATE-NC stage
 Stage 0 N/A 0 N/A 0
 Stage 1 N/A 0 N/A 0
 Stage 2 N/A 2 N/A 9
 Stage 3 N/A 28 N/A 5
Intermediate/high ADNCb 4 28 0 0

bvFTD = behavioural variant FTD; MND = motor neuron disease; N/A = not assessed; PPA = primary progressive aphasia.

a

For clinical diagnostic criteria and definitions, see ‘Materials and methods’ section.

b

According to NIA-AA neuropathological criteria (Hyman and Trojanowski, 1997).