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. 2018 Apr 27;33(8):1287–1297. doi: 10.1002/mds.27376

Table 1.

Baseline demographic and clinical characteristics of the PD and control participants

Characteristic PD Controls Difference (P Value)
N 43 35
Age (yr) 57.5 ± 8.45 56.23 ± 7.83 0.5
Male Female 35 8 27 8 0.64
H & Y stage 1.91 ± 0.48 n/a
Total MDS‐UPDRSa 45.41 ± 17.22 3.17 ± 2.7 <0.001
MDS‐UPDRS I 6.91 ± 4.71 1.80 ± 2.08 <0.001
MDS‐UPDRS II 9.21 ± 6.10 0.23 ± 0.73 <0.001
MDS‐UPDRS III 27.67 ± 11.22 1.14 ± 1.06 <0.001
MDS‐UPDRS IV 1.63 ± 2.65 0 ± 0 <0.001
MoCA 26.86 ± 2.46 28.34 ± 1.35 0.001
Mean disease duration (yr) 3.51 ± 2.86 n/a
Proportion of patients taking dopaminergic medication 81% n/a
Experiencing fluctuations (%)b 37% (30% experience at least a slight impact) n/a
MDS‐UPDRS‐defined TD and PIGD PD subtypes 29 TD; 9 PIGD; 5 indeterminate n/a
Experiencing dyskinesia (%)c 9.3% n/a

Data are mean ± SD or proportions.

a

Total MDS‐UPDRS = MDS‐UPDRS I + MDS‐UPDSR II + MDS‐UPDRS III.

b

Proportion of patients with MDS‐UPDRS 4.3 “time spent in the off state >0.”

c

Proportion of patients with MDS‐UPDRS 4.1 “time spent with dyskinesia >0.” A total of 1 PD had functional impact of dyskinesias, indicated by MDS‐UPDRS 4.2 > 0.

TD, tremor dominant. n/a, not applicable.