TABLE 1

Cohort Clinical Characteristics

VariableTotal (n = 266)WO– (n = 195)WO+ (n = 71)P
Age at onset (y)66.1 ± 9.567.0 ± 9.363.4 ± 9.60.007
Male (n)129 (48.5%)89 (45.6%)40 (56.3%)0.123
Disease duration (mo)14.1 ± 15.314.5 ± 15.912.9 ± 13.50.444
Hypertension (n)109 (41.0%)85 (43.6%)24 (33.8%)0.151
Diabetes mellitus (n)34 (12.8%)27 (13.8%)7 (9.9%)0.389
UPDRS total25.0 ± 15.525.0 ± 16.125.0 ± 13.60.994
UPDRS part 12.4 ± 2.12.4 ± 2.22.3 ± 1.80.888
UPDRS part 27.4 ± 5.17.4 ± 5.67.3 ± 3.70.938
UPDRS part 315.2 ± 10.015.1 ± 10.015.3 ± 10.00.901
Hoehn and Yahr stage1.7 ± 0.71.7 ± 0.71.6 ± 0.70.664
Time to endpoint, mo30.2 ± 14.431.4 ± 14.326.8 ± 14.20.022
LEDD (endpoint)518.7 ± 275.9473.9 ± 246.2641.6 ± 315.0<0.001
Early H/M1.66 ± 0.381.73 ± 0.401.48 ± 0.24<0.001
Late H/M1.63 ± 0.471.72 ± 0.491.40 ± 0.29<0.001
Washout rate2.4 ± 10.92.2 ± 11.53.3 ± 11.00.470
Late H/M ratio ≤ 1.78177 (66.5%)112 (57.4%)65 (91.5%)<0.001
  • Analyses were performed by an independent sample t test or a χ2 test.

  • WO = wearing-off; LEDD = levodopa equivalent daily dose.

  • Values represent mean with SD or number of subjects, with percentages in parentheses.