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. 2024 Mar 7;95(9):804–811. doi: 10.1136/jnnp-2023-332733

Table 1.

Description of the MSA sample at inclusion and over time (N=536)

Characteristic N (%) Mean±SD
At inclusion
 Sex
  Male 268 (50.0)
  Female 268 (50.0)
 Centre
  Bordeaux 308 (57.5)
  Toulouse 228 (42.5)
 Age at first symptom onset 60.6±8.1
 Age at cohort entry 65.1±8.0
 Years since first symptom onset 4.5±2.4
 Diagnosis
  MSA-C, with predominant cerebellar impairment 173 (32.3)
  MSA-P, with predominant parkinsonism 363 (67.7)
 Diagnosis certainty
  Possible 136 (25.4)
  Probable 400 (74.6)
 Orthostatic hypotension
  Presence 361 (67.4)
  Absence 175 (32.6)
 Urinary disorder
  Presence 365 (68.1)
  Absence 171 (31.9)
 Treatments
  L-dopa 366 (68.3)
  Antihypotensive treatment 161 (30.0)
  Antidepressants 111 (20.7)
 Original MSA-QoL scale
  Sum score for motor dimension/56 (n=330) 27.0±12.2
  Sum score for non-motor dimension/48 (n=344) 20.1±8.9
  Sum score for emotional/social dimension/56 (n=326) 25.6±13.0
 Modified MSA-QoL scale
  Sum score for motor dimension/44 (n=333) 25.1±9.8
  Sum score for oropharyngeal dimension/16 (n=387) 4.3±3.8
  Sum score for non-motor dimension/40 (n=350) 16.6±7.8
  Sum score for emotional/social dimension/56 (n=326) 25.6±13.0
 Disability degree (n=520)
  Completely independent (stage I) 111 (20.7)
  Not completely independent (stage II) 239 (44.6)
  More dependent (stage III) 105 (19.6)
  Very dependent (stage IV) 63 (11.8)
  Totally dependent (stage V) 2 (3.0)
During follow-up
 Visits 1501
 Visits per patient 2.8±1.9
 Years of follow-up 2.3±2.1
 Early dropout 87 (16.2)
 Death 338 (63.1)

MSA, multiple system atrophy; QoL, quality of life.