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. Author manuscript; available in PMC: 2018 Dec 1.
Published in final edited form as: Mov Disord. 2017 Oct 30;32(12):1772–1779. doi: 10.1002/mds.27198

Table 1.

Comparison of demographic, clinical, and pathologic features between PSP-CI and PSP-NC

Features Total
(N = 121)
PSP-CI
(N = 90)
PSP-NC
(N = 31)
P value
Male, No. (%) 74 (61%) 55 (61%) 19 (61%) 0.85
Age at onset, years 66 ± 8 66 ± 8 66 ± 9 0.74
Age at death, years 74 ± 8 74 ± 8 74 ± 9 0.98
Disease duration, years 7 (5, 9) 7 (5, 9) 7 (5, 12) 0.73
Family history of dementia 28 (23%) 23 (26%) 5 (16%) 0.41
Family history of Parkinsonism 21 (17%) 16 (18%) 6 (19%) 0.94
Having clinical diagnosis of PSP 91 (75%) 70 (78%) 21 (68%) 0.38
Pathology
 Brain weight, grams 1180 ± 140 1160 ± 140 1230 ± 150 0.02
 Braak NFT stage II (II, III) II (II, III) II (II, III) 0.59
 Thal amyloid phase 0 (0, 3) 0 (0, 3) 1 (0, 3) 0.20
 Alzheimer’s disease 15 (12%) 9 (10%) 6 (19%) 1.00
 Argyrophilic grain disease 31 (26%) 23 (26%) 8 (26%) 1.00
 Hippocampal sclerosis 1 (1%) 1 (1%) 0 (0%) 1.00
 Cerebrovascular pathology 14 (12%) 10 (11%) 4 (13%) 1.00
 Lewy-related pathology 9 (7%) 8 (9%) 1 (3%) 1.00
 Total tau burden 6 (4, 8) 6 (5, 8) 6 (4, 8) <0.001

Values are n (%), mean ± SD, and median (25th, 75th %-tile). Abbreviations: NFT, neurofibrillary tangle; PSP-CI, progressive supranuclear palsy with cognitive impairment; PSP-NC, progressive supranuclear palsy without cognitive impairment.