RecruitingPhase 2NCT05942716

Serotonin Control of Impulsivity in Tourette Disorder

Involvement of the Serotonergic System in the Control of Impulsivity in Tourette Disorder.


Sponsor

Hospices Civils de Lyon

Enrollment

25 participants

Start Date

Sep 24, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Tourette disorder (TD) is a neurodevelopmental disorder characterized by motor and vocal tics. It is often associated with multiple psychiatric comorbidities involving a high degree of impulsivity such as obsessive-compulsive disorders (OCD), attention-deficit hyperactivity disorders (ADHD), and intermittent explosive disorders (IED). Although a substantial body of clinical studies have emphasized the role of the dopamine system in motor symptoms, little is known about how the serotonergic (5-HT) system modulate both cognitive and affective abilities in TD. Several lines of evidence suggest that different 5-HT receptor subtypes may constitute a crucial factor in the development and maintenance of different symptoms. Because abnormal 5-HT2A receptor bindings have been reported in patients with TD and aripiprazole (drug of first choice) is a 5-HT2A antagonist, we hypothesize that 5-HT2A receptors may play an important role in regulating psychiatric symptoms in TD such as those characterized by impulsive behaviors. To investigate the involvement of 5-HT2A receptors in TD, we propose to perform a multimodal imaging study with 20 adult patients (ON and OFF treatment). Neuroimaging data will be collected with a hybrid system that simultaneously combines the positron emission tomography (PET) and the functional magnetic resonance imaging (fMRI). A highly selective PET radiotracer (\[18F\]-altanserin) will map 5-HT2A receptor bindings in the whole brain, while fMRI will provide detail information regarding the altered brain activities.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Inclusion Criteria8

  • Male or Female
  • Diagnosed with a Tourette Disorder following the DSM-5
  • Age between 18-65 years
  • Member of a social security scheme in France
  • Freely-given informed consent to participate to this study (written form)
  • With a current treatment by aripiprazole already scheduled
  • With Tics compatible with TEP/fMRI exams
  • Having (for women only) effective contraception throughout participation in the study.

Exclusion Criteria9

  • Male or Female
  • A serious not controlled psychiatric comorbidity
  • A serious, evolving or debilitating pathology with a potential influence on the study
  • Drug-taking with serotonergic effects (e.g., amphetamine, cocaine, MDMA, SSRIs, mianserin)
  • Contraindication for fMRI and PET (e.g., pacemaker, ferromagnetic implant, claustrophobia)
  • Women breastfeeding
  • Protected or restricted person (administratively or in judicial terms)
  • Participants to another study with radiations or radiotracers since less of one year, participants to a concomitant study
  • Do not speak french

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Interventions

DRUGAdministration of a PET radiotracer

A highly selective 5-HT2A receptor ligand (\[18F\]-altanserin) will be injected to patients before each PET scan. The IV injection in the arm (via a catheter) will be performed in continue during a period of 2 hours in the imaging centre (CERMEP) before the acquisition. The dose will be 2,6 MBq/kg +/- 10 % depending the prescription of the nuclear medicine. Patients will be evaluated twice, one time free of neuroleptic treatment and a second time during stable chronic treatment by neuroleptic.


Locations(2)

Service de neurologie C Hôpital neurologique Pierre Wertheimer/GHE Hospices Civils de Lyon

Bron, France

Centre de Référence Syndrome Gilles de la Tourette Département de Neurologie Pôle des Maladies du Système Nerveux Hôpital de la Pitié-Salpêtrière

Paris, France

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NCT05942716


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