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Impulse control disorders and levodopa-induced dyskinesias in Parkinson's disease: an update

期刊

LANCET NEUROLOGY
卷 16, 期 3, 页码 238-250

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/S1474-4422(17)30004-2

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资金

  1. Michael J Fox Foundation
  2. Agence Nationale de la Recherche
  3. France Parkinson
  4. Motac Neuroscience
  5. Motac Holdings
  6. National Center for Responsible Gaming
  7. National Institutes of Health
  8. Janssen
  9. Lundbeck
  10. Johnson Johnson
  11. Pfizer
  12. Alkermes
  13. Otsuka
  14. Autofony
  15. Roche
  16. Ascubio
  17. Lilly
  18. Takeda
  19. F. Hoffman La Roche
  20. Spanish Ministry of Education
  21. European Union

向作者/读者索取更多资源

Dopaminergic medications used in the treatment of patients with Parkinson's disease are associated with motor and non-motor behavioural side-effects, such as dyskinesias and impulse control disorders also known as behavioural addictions. Levodopa-induced dyskinesias occur in up to 80% of patients with Parkinson's after a few years of chronic treatment. Impulse control disorders, including gambling disorder, binge eating disorder, compulsive sexual behaviour, and compulsive shopping occur in about 17% of patients with Parkinson's disease on dopamine agonists. These behaviours reflect the interactions of the dopaminergic medications with the individual's susceptibility, and the underlying neurobiology of Parkinson's disease. Parkinsonian rodent models show enhanced reinforcing effects of chronic dopaminergic medication, and a potential role for individual susceptibility. In patients with Parkinson's disease and impulse control disorders, impairments are observed across subtypes of decisional impulsivity, possibly reflecting uncertainty and the relative balance of rewards and losses. Impairments appear to be more specific to decisional than motor impulsivity, which might reflect differences in ventral and dorsal striatal engagement. Emerging evidence suggests impulse control disorder subtypes have dissociable correlates, which indicate that individual susceptibility predisposes towards the expression of different behavioural subtypes and neurobiological substrates. Therapeutic interventions to treat patients with Parkinson's disease and impulse control disorders have shown efficacy in randomised controlled trials. Large-scale studies are warranted to identify individual risk factors and novel therapeutic targets for these diseases. Mechanisms underlying impulse control disorders and dyskinesias could provide crucial insights into other behavioural symptoms in Parkinson's disease and addictions in the general population.

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