Serotonergic dysfunction in patients with impulse control disorders in Parkinson’s disease - Scorecard - MDSpire

Serotonergic dysfunction in patients with impulse control disorders in Parkinson’s disease

  • By

  • Stéphane Prange

  • Elise Metereau

  • Hélène Klinger

  • Marine Huddlestone

  • Melinda De Oliveira

  • Sandra Duperrier

  • Pierre Courault

  • Jérôme Redoute

  • Léon Tremblay

  • Véronique Sgambato

  • Sophie Lancelot

  • Stéphane Thobois

  • March 5, 2025

  • 0 min

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Clinical Scorecard: Serotonin System Impairment in Parkinson's Disease Patients with Impulse Control Disorders

At a Glance

CategoryDetail
ConditionImpulse Control Disorders (ICDs) in Parkinson’s Disease
Key MechanismsDysregulated dopaminergic tone and serotonergic dysfunction within cortico-striato-pallido-thalamic circuits affecting inhibitory control
Target PopulationParkinson’s disease patients with impulse control disorders (PDICD+)
Care SettingNeurology and neuropsychiatry clinical settings with PET imaging capabilities

Key Highlights

  • PDICD+ patients exhibit greater presynaptic serotonin transporter (SERT) availability in posterior putamen and pallidum compared to PDICD− patients.
  • Increased cortical 5-HT2A receptor binding in sensorimotor and associative networks involved in behavioural inhibition is observed in PDICD+ patients.
  • Serotonergic dysfunction in PDICD+ specifically involves sensorimotor and associative cortico-striato-pallido-thalamic circuits, contributing to impaired inhibitory control beyond dopaminergic abnormalities.

Guideline-Based Recommendations

Diagnosis

  • Consider clinical assessment of ICD symptoms including hypersexuality, compulsive eating, shopping, and gambling in PD patients.
  • Use PET imaging with 11C-DASB and 18F-altanserin tracers to evaluate serotonergic system involvement in research or specialized centers.

Management

  • Individualize management of ICDs in PD, addressing dopaminergic treatment exposure and comorbid neuropsychiatric conditions such as anxiety and depression.
  • Employ cognitive behavioural therapy and involve patient care partners to mitigate social repercussions.
  • Avoid abrupt dopaminergic drug withdrawal to prevent withdrawal syndrome with motor and non-motor worsening.

Monitoring & Follow-up

  • Regularly monitor for emergence or worsening of ICD symptoms in PD patients, especially those on dopamine agonists.
  • Assess neuropsychiatric symptoms including depressive and anxious features that may exacerbate ICDs.

Risks

  • Dopaminergic treatments, particularly dopamine agonists, increase risk of ICD development and persistence.
  • Reduction or cessation of dopaminergic drugs may lead to withdrawal syndrome with apathy and anxiety.
  • ICDs can cause significant distress and negative social and personal consequences.

Patient & Prescribing Data

Parkinson’s disease patients with and without impulse control disorders

Dopaminergic therapies contribute to ICD risk; serotonergic dysfunction represents a potential therapeutic target beyond dopaminergic modulation.

Clinical Best Practices

  • Adopt a comprehensive, graded approach to ICD management incorporating pharmacological, psychological, and social interventions.
  • Screen for and address comorbid neuropsychiatric symptoms that may influence ICD severity.
  • Consider serotonergic system involvement when evaluating ICD pathophysiology and potential novel treatments.
  • Use PET imaging selectively in research or specialized clinical contexts to understand serotonergic contributions.

References

Original Source(s)

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