Skip to main content

Table 1 Demographic and clinical features of the MSA patients with and without camptocormia

From: Camptocormia in patients with multiple system atrophy at different disease durations: frequency and related factors

Variables

Total

With camptocormia

Without camptocormia

P value

Number

716

90 (12.6%)

626 (87.4%)

–

Diagnosis (MSA-P/MSA-C)

352/364

60/30

292/334

< 0.001*

Sex (male/female)

405/311

46/44

359/267

0.264

Age

60.18 ± 8.99

63.73 ± 7.91

59.67 ± 9.03

< 0.001*

Age of onset

57.54 ± 8.94

60.53 ± 7.81

57.11 ± 9.02

0.001*

Disease duration

2.59 ± 1.69

3.18 ± 1.67

2.50 ± 1.67

< 0.001*

Educational year

9.46 ± 3.92

9.21 ± 4.16

9.49 ± 3.89

0.522

Onset symptoms

    

Autonomic symptom

247

28

219

0.005*

Cerebellar symptom

198

15

183

Parkinsonism symptom

271

47

224

UMSARS-I

14.30 ± 6.68

17.97 ± 7.43

13.77 ± 6.40

< 0.001*#

UMSARS-II

16.98 ± 6.95

21.89 ± 7.60

16.28 ± 6.56

< 0.001*#

UMSARS-IV

2.00 ± 0.96

2.68 ± 1.17

1.90 ± 0.88

< 0.001*#

Total UMSARS score

31.28 ± 12.80

39.86 ± 14.22

30.04 ± 12.11

< 0.001*#

OH (yes/no)

198/518

28/62

170/456

0.433

Total score of FAB

14.32 ± 2.96

13.52 ± 3.47

14.44 ± 2.87

0.006*

Total MOCA score

21.57 ± 5.06

20.71 ± 6.00

21.70 ± 4.91

0.084

HDRS score

11.47 ± 8.03

13.57 ± 9.09

11.16 ± 7.83

0.008*

HARS score

9.52 ± 7.02

10.11 ± 7.27

9.43 ± 6.98

0.392

LEDD (mg/day)

137.40 ± 243.00

209.58 ± 270.48

127.02 ± 237.22

0.001*

  1. MSA multiple system atrophy, MSA-P multiple system atrophy with predominately parkinsonism, MSA-C multiple system atrophy with predominately cerebellar ataxia, UMSARS unified multiple system atrophy rating scale, OH orthostatic hypotension, FAB frontal lobe battery, MoCA Montreal cognitive assessment, HDRS Hamilton depression rating scale, HARS Hamilton anxiety rating scale, LEDD levodopa equivalent daily dose
  2. *: significant difference after adjusting by false discovery rate
  3. #: after adjusting for age of onset and disease duration