Table 1 Demographics, clinical features, and MRI findings in the various subject groups.

From: White matter and nigral alterations in multiple system atrophy-parkinsonian type

 

First cohort

  

Second cohort

  
 

HCs

PD

MSA-P

HCs

PD

MSA-P

Participants, n

n = 20

n = 19

n = 21

n = 24

n = 17

n = 10

Age, years

62.8 ± 4.7

63.1 ± 8.1

62.5 ± 11.7

65.8 ± 6.5

63.2 ± 10.2

65.3 ± 9.5

Male, % (n)

40.0% (8/20)

35.0% (7/20)

40.0% (8/20)

54.2% (13/24)

58.8% (10/17)

70.0% (7/10)

Disease duration, years

NA

5.2 ± 1.6

3.4 ± 1.7*

NA

4.7 ± 2.1

3.3 ± 0.95*

Hoehn & Yahr stage

NA

2.1 ± 0.8

3.2 ± 0.7**

NA

1.9 ± 0.7

3.0 ± 0.8**

MDS-UPDRS part 3

NA

15.3 ± 11.3

40.1 ± 16.0**

NA

18.8 ± 13.3

56.1 ± 15.3**

UMSARS part 2

NA

NA

21.2 ± 8.7

NA

NA

27.9 ± 7.3

Levodopa equivalent daily dose, mg

NA

677.0 ± 362.6

658.0 ± 310.0

NA

662.5 ± 509.1

859.1 ± 480.2

RBD present, % (n)

NA

36.8% (7/19)

47.6% (10/21)

NA

23.5% (4/17)

40.0% (4/10)

MRI findings

Pontine cross sing, % (n)

NA

0% (0/19)

9.5% (2/21)

NA

0% (0/17)

0.0% (0/10)

vertical hyperintensity line in the pons, % (n)

NA

0% (0/19)

42.1% (8/21)*

NA

0% (0/17)

10.0% (1/10)

Cerebellar atrophy, % (n)

NA

0% (0/19)

71.4% (15/21)**

NA

0% (0/17)

80.0% (8/10)**

Middle cerebellar peduncle-sign, % (n)

NA

0% (0/19)

4.8% (1/21)

NA

0% (0/17)

0.0% (0/10)

Putaminal slit, % (n)

NA

0% (0/19)

85.7% (18/21)**

NA

0% (0/17)

90.0% (9/10)**

  1. HCs healthy controls, MDS-UPDRS Movement Disorder Society Unified Parkinson’s Disease Rating Scale, MSA-P multiple system atrophy-Parkinsonian type, NA not applicable, PD Parkinson’s disease, RBD rapid eye movement-sleep behavior disorder, UMSARA part 2 Unified Multiple System Atrophy Rating Scale.
  2. *P < 0.05; MSA-P vs. PD, **P < 0.01, MSA-P vs. PD.