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. 2022 Feb 3;11(3):814. doi: 10.3390/jcm11030814

Table 1.

Demographic and clinical characteristics and psychosocial outcomes.

Characteristic ALS−
(n = 18)
ALS+
(n = 12)
PD−
(n = 19)
PD+
(n = 17)
HC
(n = 36)
Total
(n = 102)
p Value 1
Age, years 60.2 ± 9.4 56.3 ± 8.5 61.7 ± 9.1 65.6 ± 8.8 62.3 ± 8.8 61.7 ± 9.1 n. s.
Sex, male 61.1% 50.0% 63.2% 76.5% 50.0% 58.8% n. s.
Education, years 13.4 ± 2.2 15.4 ± 2.7 14.8 ± 2.3 14.9 ± 3.2 14.2 ± 3.1 14.4 ± 2.8 n. s.
Right-handedness 88.9% 100% 100% 100% 91.7% 97% n. s.
Employed 16.7% 0% 26.3% 0% 44.4% 23.5% <0.001
Disease duration (years) 2.9 ± 2.8 6.2 ± 3.7 7.4 ± 5.5 13.2 ± 6.4 - - <0.001
ALS-type, sporadic 83.3% 100% - - - - n. s.
ALS-onset, spinal:bulbar 50%:50% 75%:25% - - - - n. s.
ALS-ventilated 0% 58.3% - - - - <0.001
ALSFRS-R score a 36.4 ± 5.7 5.8 ± 6.0 - - - - <0.001
PD-equivalent - - 31.6% 47.1% - - n. s
PD-hypo-kinetic-rigid - - 42.1% 41.2% - - n. s.
PD-tremor dominant - - 26.3% 11.8% - - n. s.
H&Y score b: Median (Range) - - 2.0 (1.5 – 2.5) 3.0 (3.0 – 4.0) - - <0.001
UPDRS III-score c - - 18.1 ± 8.5 27.9 ± 7.2 - - <0.01
DBS (%) - - 10.5% 52.9% - - <0.01

Data presented as Mean ± SD (if not stated otherwise). Abbreviations: ALS, Amyotrophic lateral sclerosis; PD, Parkinson’s disease; ALSFRS, ALS-Functional Rating Scale; H&Y, Hoehn and Yahr; ALS+, ALS patients with severe motor impairment (ALSFRS-R < 20); ALS−, ALS patients with less motor impairment (ALSFRS-R > 20); PD+, PD patients with severe motor impairment (H&Y < 2.5); PD-, PD patients with less motor impairment (H&Y > 2.5); HC, healthy controls; UPDRS, Unified Parkinson’s Disease Rating Scale; DBS, deep brain stimulation. a Scores on the ALSFRS-R range from 0 to 48, with lower scores denoting a worse condition; b scores on the H&Y range from 0 to 5, with higher scores denoting a worse condition; c scores on the UPDRS III range from 0 to 108, with higher scores denoting more disability. 1 ANOVA or χ2 test or Mann–Whitney U-Test.