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Clinical Trials/NCT03114098
NCT03114098CompletedNot Applicable

Personalized Medicine: Pharmacogenetics Anomaly Research in Children and Adolescents With Pharmacological Resistance to Psychotropic Drugs

Fondation Lenval2 sites in 1 country22 target enrollmentStarted: December 7, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
22
Locations
2
Primary Endpoint
prevalence of a CYP2D6 duplication or polymorphisms

Study Overview

Brief Summary

Psychotropic drugs are frequently used in children and adolescents in France with a prescription rate of 2.5%. Antipsychotics (PA) and antidepressants (AD), each concern 0.3% of the pediatric population (Kovess et al., 2015). Despite appropriate pharmacological treatment, some patients are drug-resistant and have persisting symptoms and ineffective psychotropic treatments. These children and adolescents are generally exposed to many psychotropic molecules and often to poly-therapy.

Most psychotropic treatments, especially AP and AD, are metabolised at the hepatic level by cytochrome P450 and in particular by CYP2D6. Duplication / multiplication of the CYP2D6 gene induces too rapid metabolism of drugs.

Demonstration of a CYP2D6 abnormality has a direct impact on the management of the patient and on the clinical decisions of the clinician. Thus, knowledge of individual metabolism will decrease the failure of treatment, improve quality of life and therapeutic compliance.

Detailed Description

Psychotropic drugs are frequently used in children and adolescents in France with a prescription rate of 2.5%. Antipsychotics (PA) and antidepressants (AD) each concern 0.3% of the pediatric population (Kovess et al., 2015). Despite appropriate pharmacological treatment, some patients are drug-resistant and have persisting symptoms and ineffective psychotropic treatments. These children and adolescents are generally exposed to many psychotropic molecules and often to poly-therapy. Additionally, hospitalizations for child psychiatry, sometimes of prolonged duration, are frequent for these patients. In France, to date, the psychiatrist practitioner rarely uses pharmacogenetic evaluation as a complementary tool for prescribing psychotropic drugs. Nevertheless, an individualized prescription taking into consideration the patient's individual metabolism could greatly improve the benefit and reduce the risk of psychotropic treatments in the pediatric population.

Most psychotropic treatments, especially AP and AD, are metabolised at the hepatic level by cytochrome P450 and in particular by CYP2D6. Duplication / multiplication of the CYP2D6 gene induces too rapid metabolism of the drugs (ultrafast metabolizer). It is linked to a clinical inefficiency of treatments, and concerns up to 10% of the general population in southern Europe (Scordo et al., 2004).

In a preliminary study in Nice, an abnormality of CYP2D6 was found in 4 of the 7 patients tested with drug-resistant and / or with numerous adverse effects to the AP, of which 3 of the 5 pharmacologically resistant patients shows a duplication of the gene.

Demonstration of a CYP2D6 abnormality has a direct impact on the management of the patient and on the clinical decisions of the clinician. Thus, knowledge of individual metabolism will decrease the failure of treatment, improve quality of life and therapeutic compliance.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
— to 18 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Pharmaco resistance to psychotropic drugs
  • Obtaining the informed consent of the patient and his / her parents or legal guardian
  • Affiliation to a social security system

Exclusion Criteria

  • Patient deprived of liberty

Arms & Interventions

CYP2D6 gene abnormalities

Experimental
  • A salivary sample (2 ml sample) which will allow the investigation of an anomaly of the metabolism of psychotropic drug.
  • Blood sampling will be performed to assess treatment tolerance (6 ml). A sample (4 ml) will be kept for possible future analyzes in relation to the objectives of this study for the recruiting center of Nice.
  • Electrocardiogram
  • Clinical exam
  • Clinical Global Impression Scale (CGI-S)
  • Children's Global Assessment Scale (CGAS)
  • Sheehan Disability Scale (SDS)
  • Wechsler Preschool and Primary Scale of Intelligence III (WPPSI-III )
  • Wechsler Intelligence Scale for Children - 4 (WISC-4)
  • Wechsler Adult Intelligence Scale 4 (WAIS 4)
  • Diagnostic and Statistical Manual of Mental Disorders (DSM)
  • Autism Diagnostic Interview (ADI)

Intervention: gene abnormalities (Other)

Outcomes

Primary Outcomes

prevalence of a CYP2D6 duplication or polymorphisms

Time Frame: At baseline

study the prevalence of a CYP2D6 duplication or polymorphisms associated with an ultrafast metabolizing phenotype in a population of children and adolescents who are drug-resistant to antipsychotic and antidepressant psychotropic drugs. performed by analysis of salivar sample

Secondary Outcomes

  • New anomalies of CYP2D6 gene(At baseline)
  • Global Severity of illness(At baseline)
  • Side effects in different psychotropic treatments(At baseline)
  • Psychiatric diagnosis and comorbidities(At baseline)
  • Severity of illness for children(At baseline)
  • Description of the clinical phenotype of patients(At baseline)
  • Current and previous psychotropic treatment(At baseline)

Investigators

Sponsor
Fondation Lenval
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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