Table 1

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

CharacteristicN (%)Mean±SD
At inclusion
 Sex
  Male268 (50.0)
  Female268 (50.0)
 Centre
  Bordeaux308 (57.5)
  Toulouse228 (42.5)
 Age at first symptom onset60.6±8.1
 Age at cohort entry65.1±8.0
 Years since first symptom onset4.5±2.4
 Diagnosis
  MSA-C, with predominant cerebellar impairment173 (32.3)
  MSA-P, with predominant parkinsonism363 (67.7)
 Diagnosis certainty
  Possible136 (25.4)
  Probable400 (74.6)
 Orthostatic hypotension
  Presence361 (67.4)
  Absence175 (32.6)
 Urinary disorder
  Presence365 (68.1)
  Absence171 (31.9)
 Treatments
  L-dopa366 (68.3)
  Antihypotensive treatment161 (30.0)
  Antidepressants111 (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
 Visits1501
 Visits per patient2.8±1.9
 Years of follow-up2.3±2.1
 Early dropout87 (16.2)
 Death338 (63.1)
  • MSA, multiple system atrophy; QoL, quality of life.