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. 2000 Sep 20;11(3):131–145. doi: 10.1002/1097-0193(200011)11:3<131::AID-HBM10>3.0.CO;2-M

Table I.

Clinical data of patients

Group Duration of disease1 (mean ± SD yrs) UPDRS‐Score2 FDOPA‐uptake (Kc)3
Total I II III IV Putamen Nc.caud.
(mean ± SD) (mean ± SD)
All patients (N = 12) 7.7 ± 4.1 36.7 ± 19.3 2.6 ± 1.7 15.7 ± 7.6 16.5 ± 6.0 6.3 ± 5.4 0. 00437 ± 0. 00188 0. 00729 ± 0. 00178
Subgroup A (N = 5) 4.6 ± 2.2 19.0 ± 10.5 1.6 ± 1.7 9.8 ± 3.8 15.6 ± 4.7 2.6 ± 5.0 0. 00544 ± 0. 00243 0. 00905 ± 0. 00072
Subgroup B (N = 7) 9.9* ± 4.4 49.3* ± 12.7 3.3 ± 1.4 19.9* ± 6.9 17.1 ± 7.1 19.0* ± 4.9 0. 00366 ± 0. 00105 0. 00639* ± 0. 00104
Normals (N = 12) 0. 00967 ± 0. 00078 0. 01135 ± 0. 00115
†, *

Comparison of subgroups A an B, *indicates significant differences in the unpaired, two‐tailed t‐test.

1

Duration of disease: P < .05.

2

Unified Parkinson's disease rating scale, total: P < .01; 4 components: (I) Mentation, behavior and mood; (II) Activities of daily living: P < .05; (III) Motor examination; (IV) Complications of therapy: P < .05.

3

FDOPA‐uptake in the caudate nucleus: P < .001.