Relation between cognitive dysfunction and pseudobulbar palsy in amyotrophic lateral sclerosis

S Abrahams, L H Goldstein, A AlChalabi, A Pickering, R G Morris, R E Passingham, D J Brooks, P N Leigh

Research output: Contribution to journalArticlepeer-review

Abstract

Objectives-To examine the relation between cognitive dysfunction and pseudobulbar features in patients with amyotrophic lateral sclerosis (ALS).

Methods-The performance of two patient groups, ALS with pseudobulbar palsy (n = 24) and ALS without pseudobulbar palsy (n = 28), was compared with 28 healthy age matched controls on an extensive neuropsychological battery. Tests used were the national adult reading test, short form of the WAIS-R, recognition memory rest, Kendrick object learning test, paired associate learning, Wisconsin card sorting test, verbal fluency, Stroop and negative priming tests, a random movement joystick test, and a computerised Tower of Hanoi test.

Results-Tests of executive function showed a pronounced deficit on written verbal fluency in both ALS groups in comparison to controls, which tended to be more prominent in patients with ALS with pseudobulbar palsy. The random movement joystick test (a non-verbal test of intrinsic movement generation) showed an impairment in the generation of random sequences in patients with pseudobulbar palsy only. The computerised Tower of Hanoi showed a subtle planning impairment (shorter planning times) in all the patients with ALS compared with controls on trials requiring more complex solutions. In addition the pseudobulbar patients displayed shorter planning times on complex trials, and tended to solve these trials less accurately. There was also evidence of a deficit for all patients with ALS in comparison with controls on total errors and number of categories achieved on the Wisconsin card sorting test and a strong tendency towards an impairment on a task of selective attention and cognitive inhibition (negative priming). A word recognition memory deficit was showed across both ALS groups.

Conclusions-This study elicited cognitive deficits (involving predominantly executive processes, with some evidence of memory impairment) in patients with ALS and further strengthened the link between ALS and frontal lobe dysfunction, this being more prominent in patients with pseudobulbar palsy, However, cognitive impairments suggestive of extramotor cortical involvment were not exclusive to this subgroup.

Original languageEnglish
Pages (from-to)464-472
Number of pages9
JournalJournal of Neurology Neurosurgery & Psychiatry
Volume62
Issue number5
Publication statusPublished - May 1997

Keywords

  • amyotrophic lateral sclerosis
  • pseudobulbar palsy
  • neuropsychological impairment
  • executive dysfunction
  • MOTOR-NEURON DISEASE
  • POSITRON EMISSION TOMOGRAPHY
  • FRONTAL-LOBE FUNCTION
  • COMPUTED-TOMOGRAPHY
  • PLANNING ABILITY
  • LIMBIC SYSTEM
  • DEMENTIA
  • ACTIVATION
  • ATTENTION
  • SCHIZOPHRENIA

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