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. 2017 Sep 4;8:457. doi: 10.3389/fneur.2017.00457

Table 1.

Demographic and clinical data of the training and test groups.

PD patients Older adults
Lab assessment
Training cohort 1
N (females) 3 (2) 2 (1)
Age (years) 72.3 (4.7) 71.0 (2.8)
MDS-UPDRS III (0–132) 26 (15) 2 (2)
H&Y (0–5) 2 (1) 0 (0)
LED (mg) 640 (353) 0 (0)
Test cohort 1
N (females) 11 (5) 12 (4)
Age (years) 74.7 (7.2) 70.8 (3.0)
MDS-UPDRS III (0–132) 39 (9) 1 (2)
H&Y (0–5) 3 (1) 0 (0)
LED (mg) 540 (298) 0 (0)
Home-like assessment
Training cohort 2
N (females) 4 (2) 2 (1)
Age (years) 69.3 (3.6) 63.0 (17.0)
MDS-UPDRS III (0–132) 20 (8) 1 (0)
H&Y (0–5) 2 (1) 0 (0)
LED (mg) 683 (735) 0 (0)
Test cohort 2
N (females) 21 (11) 12 (6)
Age (years) 66.4 (9.0) 58.4 (8.9)
MDS-UPDRS III (0–132) 32 (12) 2 (4)
H&Y (0–5) 3 (1) 0 (0)
LED (mg) 841 (604) 0 (0)

Data are shown as mean ± SD, except gender.

H&Y, Hoehn and Yahr; LED, Levodopa equivalent dose; PD, Parkinson’s disease; MDS-UPDRS III, motor part of the revised Unified PD Rating scale.