TABLE 1

Demographic Characteristics of Patient Groups According to the 1-Year Clinical Follow-up Diagnosis

Clinical diagnosisF/M (n)Age (y)Symptom duration (y)Clinical follow-up (mo)H&Y scoreUPDRS-III scoreMMSE score
LBD16/1865.0 (13.7)3.6 (2.5)12.1 (6.2)2.7 (1.2)*29.8 (13.7)26.4 (4.6)
PD10/1361.6 (14.6)4.1 (2.2)10.8 (6.1)2.5 (1.2)28.7 (14.1)28.2 (2.4)§
PDD/DLB6/572.0 (8.4)c2.3 (2.6)14.6 (5.8)3.1 (1.2)32.0 (13.3)22.9 (5.7)§
APS23/2167.9 (8.5)3.3 (1.9)11.3 (4.4)3.5 (0.9)*33.1 (14.8)26.7 (3.6)
MSA8/565.5 (7.1)3.5 (2.0)9.6 (3.1)3.5 (0.7)33.3 (15.6)28.4 (1.7)§
PSP/CBD15/1668.9 (8.9)3.2 (1.8)12.1 (4.7)3.5 (1.0)33.0 (14.7)26.0 (4.0)
  • * Wilcoxon test LBD vs. APS, P = 0.002.

  • ANOVA across subgroups, P = 0.029, post hoc Tukey-Kramer honestly significant difference test indicated significantly higher age in PDD/DLB than in PD (P < 0.05).

  • Kruskal–Wallis test across subgroups, P = 0.071, post hoc Wilcoxon test indicated significantly higher H&Y score in MSA (corrected P = 0.03) and PSP/CBD (corrected P = 0.01) than in PD.

  • § ANOVA across subgroups, P = 0.0009, post hoc Tukey-Kramer honestly significant difference test indicated significantly lower MMSE in PDD/DLB than in PD and MSA (P < 0.05).

  • UPDRS-III = Unified Parkinson Disease Rating Scale, part III (motor score).

  • Data are given as mean value followed by SD in parentheses, except for sex (F/M). Clinical follow-up refers to time between PET imaging and clinical diagnosis; other data refer to time of PET imaging, except MMSE: scores were available in 67 patients, in 23 patients only at follow-up. In the latter, 17 patients still showed normal scores (≥27). Availability of MMSE data did not differ between patient groups (P > 0.1).