Evolution of neuropsychological profile in motor subtypes of multiple system atrophy

Parkinsonism Relat Disord. 2020 Jan:70:67-73. doi: 10.1016/j.parkreldis.2019.12.010. Epub 2019 Dec 19.

Abstract

Introduction: Cognitive deficits and neuropsychiatric symptoms occur in parkinsonian and cerebellar subtypes of Multiple System Atrophy (MSA-P and MSA-C). These symptoms have been investigated mainly in cross-sectional studies. The present 1-year follow-up study aimed at evaluating the evolution of cognitive and neuropsychiatric profile in patients with MSA-C and MSA-P.

Methods: Twenty-nine patients with MSA-P, 21 with MSA-C and 30 healthy subjects (HCs) underwent a neuropsychological battery and questionnaires assessing depression and apathy (T0). After 1 year (T1), patients with MSA-C and MSA-P underwent the same neuropsychological and neuropsychiatric tools employed at T0.

Results: At T0, MSA-P and MSA-C groups were more depressed and apathetic and performed worse on tests assessing repetition abilities, executive and attentive functions than HCs. MSA-P and MSA-C groups did not differ on cognitive variables and neuropsychiatric scales. At T1, a significant worsening in spatial planning and psychomotor speed in MSA-C group and a significant worsening in memory, spatial planning, repetition abilities and functional autonomy in MSA-P group were found. The prevalence of apathy increased in both subtypes, whereas the prevalence of depression was reduced in MSA-C and relatively consistent in MSA-P.

Conclusions: The finding revealed a wide-ranging worsening of cognitive functions in MSA-P and a significant decline in processing speed in MSA-C. These results underline the relevance of evaluating cognitive and psychiatric features of MSA over the course of the disease in the daily clinical practice.

Keywords: Apathy; Cognitive deficits; Depression; Multiple system atrophy.

MeSH terms

  • Aged
  • Apathy / physiology*
  • Cognitive Dysfunction / etiology
  • Cognitive Dysfunction / physiopathology*
  • Dementia / etiology
  • Dementia / physiopathology*
  • Depression / etiology
  • Depression / physiopathology*
  • Disease Progression*
  • Executive Function / physiology
  • Female
  • Follow-Up Studies
  • Humans
  • Male
  • Middle Aged
  • Multiple System Atrophy / complications
  • Multiple System Atrophy / physiopathology*
  • Neuropsychological Tests
  • Psychomotor Performance / physiology