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Pharmacogenetics Anomaly Research in Children and Adolescents With Pharmacological Resistance to Psychotropic Drugs (M4P)

Primary Purpose

Drug Resistance, Psychotropic Drugs

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
gene abnormalities
Sponsored by
Fondation Lenval
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Drug Resistance focused on measuring Drug Resistance, CYP2D6, cytochrom P450

Eligibility Criteria

undefined - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Fondation Lenval Hôpitaux Pédiatriques de Nice CHU-LENVAL

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

CYP2D6 gene abnormalities

Arm Description

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)

Outcomes

Primary Outcome Measures

prevalence of a CYP2D6 duplication or polymorphisms
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 Outcome Measures

Psychiatric diagnosis and comorbidities
Diagnostic and Statistical Manual of Mental Disorders 5 DSM5
Global Severity of illness
Clinical Global Impression scale (échelle CGI-I)
Severity of illness for children
Children's Global Assessment Scale (CGAS)
Current and previous psychotropic treatment
Number of different molecules (antipsychotic antidepressant) used during the therapeutic history of the patient, duration of treatment with each molecule, type and maximum dose of current and previous psychotropic treatments.
Side effects in different psychotropic treatments
Type and severity of the adverse effects identified during the various psychotropic treatments will be collected. This collection will be carried out through the interrogation and study of the medical file
New anomalies of CYP2D6 gene
To look for any other abnormality of the CYP2D6 gene not known to be associated with an ultrafast metabolizing phenotype
Description of the clinical phenotype of patients
The characterization of the clinical phenotype will be carried out on the one hand by the standardized diagnostic interview MINI Mini International Neuropsychiatric Interview

Full Information

First Posted
February 22, 2017
Last Updated
February 25, 2019
Sponsor
Fondation Lenval
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1. Study Identification

Unique Protocol Identification Number
NCT03114098
Brief Title
Pharmacogenetics Anomaly Research in Children and Adolescents With Pharmacological Resistance to Psychotropic Drugs
Acronym
M4P
Official Title
Personalized Medicine: Pharmacogenetics Anomaly Research in Children and Adolescents With Pharmacological Resistance to Psychotropic Drugs
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
December 7, 2016 (Actual)
Primary Completion Date
December 12, 2018 (Actual)
Study Completion Date
January 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fondation Lenval

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Drug Resistance, Psychotropic Drugs
Keywords
Drug Resistance, CYP2D6, cytochrom P450

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
22 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CYP2D6 gene abnormalities
Arm Type
Experimental
Arm Description
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 Type
Other
Intervention Name(s)
gene abnormalities
Intervention Description
A salivary sample (2 ml sample) Blood sampling will be performed to assess treatment tolerance (6 ml)
Primary Outcome Measure Information:
Title
prevalence of a CYP2D6 duplication or polymorphisms
Description
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
Time Frame
At baseline
Secondary Outcome Measure Information:
Title
Psychiatric diagnosis and comorbidities
Description
Diagnostic and Statistical Manual of Mental Disorders 5 DSM5
Time Frame
At baseline
Title
Global Severity of illness
Description
Clinical Global Impression scale (échelle CGI-I)
Time Frame
At baseline
Title
Severity of illness for children
Description
Children's Global Assessment Scale (CGAS)
Time Frame
At baseline
Title
Current and previous psychotropic treatment
Description
Number of different molecules (antipsychotic antidepressant) used during the therapeutic history of the patient, duration of treatment with each molecule, type and maximum dose of current and previous psychotropic treatments.
Time Frame
At baseline
Title
Side effects in different psychotropic treatments
Description
Type and severity of the adverse effects identified during the various psychotropic treatments will be collected. This collection will be carried out through the interrogation and study of the medical file
Time Frame
At baseline
Title
New anomalies of CYP2D6 gene
Description
To look for any other abnormality of the CYP2D6 gene not known to be associated with an ultrafast metabolizing phenotype
Time Frame
At baseline
Title
Description of the clinical phenotype of patients
Description
The characterization of the clinical phenotype will be carried out on the one hand by the standardized diagnostic interview MINI Mini International Neuropsychiatric Interview
Time Frame
At baseline

10. Eligibility

Sex
All
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Susanne THÜMMLER, MD
Organizational Affiliation
Fondation Lenval Hôpitaux Pédiatriques de Nice CHU-LENVAL
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fondation Lenval Hôpitaux Pédiatriques de Nice CHU-LENVAL
City
Nice
ZIP/Postal Code
06200
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

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

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