Table 1:
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