Skip to main content
[Preprint]. 2023 Feb 2:2023.01.31.23285242. [Version 1] doi: 10.1101/2023.01.31.23285242

Table 1:

Demographic information for all individuals included in this study, stratified by TDP-43 diagnosis.

ALS FTLD-TDP LATE-AD+ LATE-AD-
N 141 126 235 69
Age at Onset 59.5 (11.0) 61.0 (9.0) 70.2 (9.0) 68.8 (10.0)
Age at Death 63.7 (10.6) 68.5 (10.0) 80.9 (8.4) 80.9 (8.7)
Disease Duration 4.3 (4.3) 7.3 (4.1) 10.3 (4.3) 11.9 (8.0)
% Female 40.4% 45.2% 62.1% 31.9%
Braak Stage 1.7 (1.7) 2.0 (1.6) 5.8 (0.7) 3.3 (1.4)
% APOE4 Carrier 25.0% 24.6% 63.3% 33.8%
% APOE2 Carrier 12.9% 18.2% 5.2% 8.8%
% Mutation Carrier 19.9% 46.8% 4.2% 5.8%
% Copathology 76.6% 88.9% 42.7% 55.1%
% AD Phenotype 0.0% 12.7% 77.4% 8.7%
% FTDS Phenotype 1.4% 81.7% 9.4% 15.9%
% MND Phenotype 96.5% 0.0% 0.0% 1.4%
% LBD Phenotype 0.7% 0.8% 4.3% 62.3%
% Other Phenotype 1.4% 4.8% 9.0% 11.6%
PMI 12.6 (7.9) 12.8 (7.3) 12.6 (7.1) 11.5 (6.7)

“LATE-AD-” = non-Alzheimer’s individuals with amygdalar but not medullar TDP-43 pathology. “Copathology” = Demonstrates at least one secondary copathology (other than LATE). AD = Alzheimer’s Disease; FTDS = Frontotemporal dementia spectrum; MND = Motor Neuron Disease; LBD = Lewy Body Disease; PMI = Postmortem Interval