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. Author manuscript; available in PMC: 2019 Sep 1.
Published in final edited form as: Acta Neuropathol. 2018 Jun 20;136(3):389–404. doi: 10.1007/s00401-018-1878-z

Table 2: Cluster analyses by TDP-43 pathology and clinicopathologic associations.

TDP-negative
N = 103
TDP-limited
N = 44
TDP-severe
N = 40
P value
Male, No. (%) 54 (52%) 21 (48%) 15 (38%) 0.284
Age at death, years 69 ± 8 70 ± 7 72 ± 9 0.226
Brain weight, g 1130 ± 130 1090 ± 160 1100 ± 160 0.337
Thickness of corpus callosum, mm 3.4 ± 1.1 3.4 ± 1.0 3.4 ± 1.0 0.987
Braak neurofibrillary tangles stage II (I, III) II (I, III) II (I, III) 0.771
Thal amyloid phase 0 (0, 2) 0 (0, 1) 0 (0, 1) 0.813
Alzheimer disease 7 (7%) 2 (5%) 2 (5%) 0.919
Hippocampal sclerosis 0 (0%) 1 (2%) 1 (3%) 0.200
Argyrophilic grain disease 41 (40%) 21 (48%) 25 (63%) 0.046
Lewy-related pathology 5 (5%) 2 (5%) 5 (13%) 0.234
Clinical characteristics
 Disease duration, years 6 ± 3 7 ± 2 7 ± 4 0.396
 Clinical diagnosis of CBS 48/102 (47%) 17/44 (39%) 4/40 (10%) 7.4×10−5
 Clinical diagnosis of PSP 31/102 (30%) 14/44 (32%) 32/40 (80%) 1.4×10−7
 Diagnostic physician type 0.799
 Movement disorder specialist 45/95 (47%) 19/41 (46%) 18/38 (47%)
 Dementia specialist 10/95 (11%) 7/41 (17%) 3/38 (8%)
 General neurologist 36/95 (38%) 14/41 (34%) 14/38 (37%)
 Non-neurologist 4/95 (4%) 1/421 (2%) 3/38 (8%)
 Downward gaze palsy 30/89 (34%) 13/37 (35%) 29/34 (85%) 4.3×10−7
 Asymmetric rigidity/apraxia 51/69 (74%) 20/29 (69%) 15/23 (65%) 0.766
 Initial presentations 0.231
 Motor symptoms 48/84 (57%) 17/35 (49%) 12/29 (41%)
 Cognitive/behavioral symptoms 20/84 (24%) 14/35 (40%) 9/29 (31%)
 Mixed 16/84 (19%) 4/35 (11%) 8/29 (28%)

Data are displayed as n (%), mean ± SD, and median (25th, 75th range).