Table 1

Summary of baseline clinical characteristics, CSF NF-L and clinical progression data

Cohort 1Cohort 2
PSP
(n=33)
CBS
(n=11)
MSA
(n=29)
PD
(n=25)
CON
(n=30)
PSP
(n=21)
CBS
(n=11)
MSA
(n=9)
PD
(n=12)
CON
(n=4)
Gender male/female (%)48/5257/4355/4564/3650/5081/1918/8289/1167/3325/75
Age at motor symptom onset (years)—mean, SD65.1*
6.2
64.5*
8.0
60.2*
5.9
55.8‡
8.1
63.6*
6.2
59.4*
7.8
61.0*
9.2
50.7‡
6.0
Age at LP (years)—mean, SD69.6†
5.9
68.4†
8.4
64.4†
5.8
67.4†‡
9.1
59.8*
9.9
67.2*
5.7
64.1*
7.5
65.6*
8.7
59.9†‡
6.1
65.0*
2.9
Disease duration at LP (years)—mean, SD4.5*
2.5
3.9*
1.2
4.2*
2.2
11.6
6.1
3.6*
2.0
4.7*
1.9
4.6*
2.6
9.2
3.1
PSPRS score—mean, SD42.0‡
11.5
38.9
15.2
30.6‡
9.1
30.4
10.8
CSF NF-L concentration (ng/L)—mean, SD2225.2
*†‡§
913.4
2268.6
*†
1291.4
2991.0
*†‡
1462.2
963.0

565.8
630.6
*
278.9
3228.5
*†‡
1611.3
2547.3
*†§
1255.7
4671.6
*†‡
2768.9
980.3
218.7
868.5
236.4
% of subjects deceased at point of censoring8864864824000
Total disease duration in deceased group
(years)—mean, SD
7.2*
2.5
7.0*
2.5
7.1*
2.4
13.7
6.8
6.0
2.3
NANANA
No of pathologically confirmed cases9
PSP=9
2
CBD=2
6
MSA=5
PSP=1
02
PSP=2
NANANA
  • Only statistically significant (p<0.05) differences between continuous variables are noted from t-tests.

  • *vs PD in same cohort.

  • †vs controls in same cohort.

  • ‡vs same measure in other cohort.

  • §vs MSA in same cohort.

  • CBS, corticobasal syndrome; CON, controls; CSF, cerebrospinal fluid; LP, lumbar puncture; MSA, multiple system atrophy; NA, data not available; NF-L, neurofilament light chain; PD, Parkinson’s disease; PSP, progressive supranuclear palsy; PSPRS, PSP rating scale.