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. 2023 Jan 11;50(5):1395–1405. doi: 10.1007/s00259-022-06104-0

Table 1.

General characteristics of the study participants

Entire cohort of patients with PSP PSP-RS PSP-non-RS Healthy controls p* p#
Number of subjects 148 84 64 20  −   − 
Sex (men/women) 83/65 43/41 40/24 6/14 0.03a 0.17a
Age (years) 65.7 ± 6.8 66.3 ± 5.8 65.0 ± 7.8 56.7 ± 7.3  < 0.01b 0.24b
Age at onset (years) 62.0 ± 7.1 63.0 ± 6.2 60.8 ± 8.0 N.A  −  0.07b
Disease duration (months) 38.0 (22.0,60.0) 38.0 (24.0, 52.0) 42.0 (18.0, 72.0) N.A  −  0.46c
PSPrs score 28.0 (20.0, 37.5) 32.0 (22.0, 43.0) 23.5 (17.0, 31.0) N.A  −   < 0.01c
MMSE score 25 (21, 27) 24 (19, 27) 26 (24, 28) 28 (27, 29)  < 0.01c  < 0.01c
Education (years) 9.0 (8.0, 12.0) 9.0 (6.0, 12.0) 11.0 (8.0, 12.3) 12.0 (9.0,15.8) 0.01c 0.12c
LEDD (mg)

400.0

(150.0, 600.0)

400.0

(150.0, 600.0)

400.0

(225.0, 650.0)

N.A  −  0.65c

Data are expressed as means ± standard deviations or medians (interquartile ranges), unless otherwise state. Abbreviations: PSP, progressive supranuclear palsy; PSP-RS, progressive supranuclear palsy-Richardson’s syndrome; PSP-non-RS, other PSP subtypes with the exception of progressive supranuclear palsy-Richardson’s syndrome; PSPrs, progressive supranuclear palsy rating scale; MMSE, Mini-Mental State Examination; LEDD, L-dopa equivalent daily dose; N.A., not applicable

* Patients with PSP versus healthy controls; # Patients with PSP-RS versus patients with PSP-non-RS

a Chi-square test; b Student’s t-test; c Mann–Whitney U test