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. 2023 Nov 23;11(3):220–226. doi: 10.1002/mdc3.13925

TABLE 1.

Patients' characteristics and comparison between groups

Variable All patients Comparison based on MSA type Comparison based on initial symptom
Mean ± SD or frequency (n = 20) MSA‐P (n = 13) MSA‐C (n = 7) P‐value Motor impairment only (n = 10) Autonomic failure (n = 10) P‐value
Demographics (y)
Age of onset (n = 20) 38.58 ± 2.12 38.4 ± 2.3 38.9 ± 1.7 0.75 38.7 ± 1.6 38.47 ± 2.6 0.85
Time from onset to diagnosis (n = 20) 6.66 ± 4.53 6.9 ± 5.03 6.06 ± 3.7 0.64 8.28 ± 5.1 5.04 ± 3.3 0.07
Time from diagnosis to death 2.97 ± 1.99 3.1 ± 2.01 2.55 ± 2.09 0.72 3.2 ± 2.2 2.79 ± 1.9 0.88
Time from onset to death 9.06 ± 4.02 9.4 ± 4.6 8.1 ± 2.08 0.50 10.8 ± 4.02 7.8 ± 3.7 0.13
Age of  death 47.77 ± 3.70 47.87 ± 4.2 47.5 ± 2.3 0.95 49.8 ± 4.5 46.3 ± 2.1 0.08
Autonomic function testing
TST (%) 66.57 ± 38.58 71.07 ± 34.6 55.7 ± 49.5 0.57 67.5 ± 39.8 65.5 ± 39.7 1
CASS‐A 4.78 ± 2.25 5.07 ± 2.2 4.1 ± 2.4 0.42 4.5 ± 2.3 5 ± 2.2 0.58
CASS‐T 5.93 ± 2.40 6.1 ± 2.08 5.25 ± 3.5 0.66 5.5 ± 2.4 6.3 ± 2.4 0.39
Clinical features
LEDD (last visit) 1013.33 ± 859.99 1083.33 ± 940.67 733.33 ± 404.14 0.94 986.33 ± 826.98 1053.83 ± 986.56 0.81
Presence of dystonia 8 (40%) 7 (53.8%) 1 (14.3%) 0.15 6 (60%) 2 (20%) 0.16
Positive Babinski 5 (25%) 2 (15.4%) 3 (42.9%) 0.28 2 (20%) 3 (30%) 1
Hyperreflexia 11 (55%) 7 (53.8%) 5 (71.4%) 0.64 7 (70%) 5 (50%) 0.64

Abbreviations: MSA, multiple system atrophy; SD, standard deviation; MSA‐P, multiple system atrophy‐parkinsonism; MSA‐C, multiple system atrophy‐cerebellar ataxia; TST, thermoregulatory sweat test; CASS‐A, Composite Autonomic Severity Score using findings from autonomic reflex screen only; CASS‐T, Composite Autonomic Severity Score using findings from both autonomic reflex screen and thermoregulatory sweat test; LEDD, levodopa equivalent daily dose.