4.7 Article

Drug-induced deactivation of inhibitory networks predicts pathological gambling in PD

Journal

NEUROLOGY
Volume 75, Issue 19, Pages 1711-1716

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0b013e3181fc27fa

Keywords

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Funding

  1. Ontario Problem Gambling Research Centre
  2. Canadian Institutes of Health Research (CIHR) [MOP-64423]
  3. Fondazione Grigioni per il Morbo di Parkinson
  4. Bioscan
  5. Ontario Ministry of Research and Innovation
  6. Canada Foundation for Innovation
  7. CIHR
  8. Teva Pharmaceutical Industries Ltd.
  9. Boehringer Ingelheim
  10. Solvay Pharmaceuticals, Inc.
  11. Solstice Neurosciences, Inc.
  12. Impax Laboratories
  13. Neurogen
  14. Medivation, Inc.
  15. National Parkinson Foundation
  16. Parkinson Society Canada
  17. Michael J. Fox Foundation
  18. Huntington Study Group
  19. Taro Pharma
  20. Dystonia Medical Research Foundation
  21. Parkinson's Disease Foundation

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Objective: Some patients with Parkinson disease (PD) develop pathological gambling when treated with dopamine agonists (DAs). However, little is known about DA-induced changes in neuronal networks that may underpin this drug-induced change in behavior in vulnerable individuals. In this case-control study, we aimed to investigate DA-induced changes in brain activity that may differentiate patients with PD with DA-induced pathological gambling (gamblers) from patients with PD without such a history (controls). Methods: Following overnight withdrawal of antiparkinsonian medication, patients were studied with (H2O)-O-15 PET before and after administration of DA (3 mg apomorphine) to measure changes in regional cerebral blood flow as an index of regional brain activity during a card selection game with probabilistic feedback. Results: We observed that the direction of DA-related activity change in brain areas that are implicated in impulse control and response inhibition (lateral orbitofrontal cortex, rostral cingulate zone, amygdala, external pallidum) distinguished gamblers from controls. DA significantly increased activity in these areas in controls, while gamblers showed a significant DA-induced reduction of activity. Conclusions: We propose that in vulnerable patients with PD, DAs produce an abnormal neuronal pattern that resembles those found in nonparkinsonian pathological gambling and drug addiction. DA-induced disruption of inhibitory key functions-outcome monitoring (rostral cingulate zone), acquisition and retention of negative action-outcome associations (amygdala and lateral orbitofrontal cortex)-together with restricted access of those areas to executive control (external pallidum)-may well explain loss of impulse control and response inhibition in vulnerable patients with PD, thereby fostering the development of pathological gambling. Neurology(R) 2010;75:1711-1716

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