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. Author manuscript; available in PMC: 2024 Feb 16.
Published in final edited form as: Ann Neurol. 2023 Sep 5;94(6):1036–1047. doi: 10.1002/ana.26762

TABLE 1.

Group Characteristics

Sex (% male) Age at death (mean yr; SD) Age at onset (mean yr; SD) PMI (mean h; SD) Brain weight (g; SD) Braak stage V/VI (%) Aβ plaque score (A3; %) APOE E4 (%)
AD (n = 14) 57 81 (11) 72 (14) 19 (9) 1,197 (131) 78% 86% 33%
AD/TDP (n = 16) 44 80 (9) 69 (12) 18 (5) 1,141 (132) 81% 100% 39%
FTLD-TDP (n = 18) 50 68 (9) 59 (9) 13 (10) 1,039 (227) 0% 0% 4%
TDP type A (n = 5) 60 70 (10) 64 (12) 6 (2) 970 (77) 0% 0% 0%
TDP type B (n = 5) 80 67 (14) 59 (6) 16 (10) 1,370 (137) 0% 0% 0%
TDP type C (n = 8) 25 68 (4) 55 (5) 14 (11) 1,040 (232) 0% 0% 6%

Note: APOE genotyping was available for 38 participants and frequencies reflect the proportion of E4 allele present. A3 = severe amyloid-β score criteria according to the NIA-AA; AD = Alzheimer’s disease; AD/TDP = comorbid Alzheimer’s disease and transactive response DNA-binding protein 43; APOE E4 = apolipoprotein allele 4; FTLD-TDP = transactive response DNA-binding protein 43 pathology form of frontotemporal lobar degeneration; PMI = post-mortem interval; TDP = transactive response DNA-binding protein 43; h = hours; yr = years; SD = standard deviation.