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. 2024 Apr 15;30(4):1096–1103. doi: 10.1038/s41591-024-02886-y

Table 2.

Baseline demographic and clinical characteristics of the whole study population, participants taking MAO-B inhibitors at baseline and those who were treatment-naive at baseline

Whole population MAO-B inhibitors Treatment-naive
Placebo (n = 105) Prasinezumab pooled (n = 211) Placebo (n = 38) Prasinezumab pooled (n = 77) Placebo (n = 67) Prasinezumab pooled (n = 134)
Age (years), mean (s.d.) 59.9 (8.7) 59.9 (9.3) 58.3 (8.4) 58.2 (9.4) 60.8 (8.8) 60.9 (9.2)
Sex (male), n (%) 71 (67.6) 142 (67.3) 24 (63.2) 50 (64.9) 47 (70.1) 92 (68.7)
Time since diagnosis (months), mean (s.d.) 9.95 (6.79) 10.19 (6.37) 11.93 (6.37) 11.98 (5.99) 8.83 (6.81) 9.17 (6.37)
Time since diagnosis ≤12 months, n (%) 72 (68.6) 147 (69.7) 22 (57.9) 47 (61.0) 50 (74.6) 100 (74.6)
Hoehn and Yahr stage, n (%)
 Stage I 20 (19.0) 58 (27.5) 7 (18.4) 25 (32.5) 13 (19.4) 33 (24.6)
 Stage II 85 (81.0) 153 (72.5) 31 (81.6) 52 (67.5) 54 (80.6) 101 (75.4)
MDS-UPDRS total (sum of Parts I, II and III), mean (s.d.) 32.01 (12.98) 31.11 (12.70) 32.16 (12.01) 29.25 (11.90) 31.93 (13.58) 32.19 (13.06)
MDS-UPDRS Part I, mean (s.d.) 4.91 (3.71) 4.45 (3.88) 5.08 (3.82) 4.19 (3.15) 4.82 (3.67) 4.60 (4.25)
MDS-UPDRS Part II, mean (s.d.) 5.55 (4.09) 5.22 (4.03) 5.84 (4.25) 4.87 (3.69) 5.39 (4.01) 5.43 (4.21)
MDS-UPDRS Part III, mean (s.d.) 21.54 (9.11) 21.44 (8.97) 21.24 (8.77) 20.18 (8.87) 21.72 (9.36) 22.16 (8.98)
DaT-SPECT SBRa, mean (s.d.) 1.06 (0.30) 1.06 (0.34) 1.03 (0.30) 1.02 (0.31) 1.09 (0.29) 1.09 (0.35)
Estimated average change in MDS-UPDRS Part III per month before the study (points per month) 2.16 2.10 1.78 1.68 2.46 2.42

n is the number of participants contributing to summary statistics. Percentages are based on n.

aIpsilateral putamen. DaT-SPECT, dopamine transporter-single-photon emission computed tomography; MAO-B, monoamine oxidase-B; MDS-UPDRS, Movement Disorder Society-Unified Parkinson’s Disease Rating Scale; s.d., standard deviation; SBR, striatal binding ratio.