Neural mechanisms underlying cognitive inflexibility in Parkinson's disease

Neuropsychologia. 2016 Dec;93(Pt A):142-150. doi: 10.1016/j.neuropsychologia.2016.09.021. Epub 2016 Sep 28.

Abstract

Cognitive inflexibility is a hallmark of executive dysfunction in Parkinson's disease (PD). This deficit consistently manifests itself in a PD-related increase in the number of perseverative errors committed on the Wisconsin Card Sorting Test (WCST). However, the neural processes underlying perseverative WCST performance in PD are still largely unknown. The present study is the first to investigate the event-related potential (ERP) correlates of cognitive inflexibility on the WCST in PD patients. Thirty-two PD patients and 35 matched control participants completed a computerized version of the WCST while the electroencephalogram (EEG) was recorded. Behavioral results revealed the expected increase in perseverative errors in patients with PD. ERP analysis focused on two established indicators of executive processes: the fronto-central P3a as an index of attentional orienting and the sustained parietal positivity (SPP) as an index of set-shifting processes. In comparison to controls, P3a amplitudes were significantly attenuated in PD patients. Regression analysis further revealed that P3a and SPP amplitudes interactively contributed to the prediction of perseverative errors in PD patients: The number of perseverative errors was only increased when both ERP amplitudes were attenuated. Notably, the two ERP markers of executive processes accounted for more than 40% of the variance in perseverative errors in PD patients. We conclude that cognitive inflexibility in PD occurs when the neural bases of multiple executive processes are affected by the pathophysiology of PD. The combined measurement of P3a and SPP might yield an electrophysiological marker of cognitive inflexibility in PD.

Keywords: Cognitive flexibility; Event-related potentials; Executive functioning; Parkinson's disease; Set shifting; Wisconsin Card Sorting Test.

MeSH terms

  • Brain / physiopathology*
  • Cognition / physiology*
  • Electroencephalography
  • Evoked Potentials
  • Executive Function / physiology*
  • Feedback, Psychological / physiology
  • Female
  • Humans
  • Male
  • Middle Aged
  • Neuropsychological Tests
  • Parkinson Disease / physiopathology*
  • Parkinson Disease / psychology*
  • Reaction Time
  • Regression Analysis
  • Signal Processing, Computer-Assisted