Familial and Functional Study of Genetic Variants Identified in People With Schizophrenia, Bipolar Disorder, Autism Spectrum Disorder or Resistant Depression
NCT ID: NCT05480826
Last Updated: 2024-04-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
50 participants
INTERVENTIONAL
2023-03-15
2028-09-15
Brief Summary
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The present project aims to enrich existing biocollections with DNA from blood or saliva from relatives of patients identified with genetic variants. In addition, we wish to collect hair follicules from patients with identified genetic variants of interest and their family members who wish to participate in the study. These hair samples with SNA will be used to dedifferentiate the isolated cells into induced pluripotent stem cells (IPSCs), and then to differentiate them into cells expressing the gene of interest, such as neurons or astrocytes, or into more complex systems, such as brain organoids.
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
* patients with a mental disorder
* relatives of patients included
OTHER
SINGLE
Study Groups
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Patients
Subject suffering from (according to DSM IV criteria)
* bipolar disorder
* unipolar depression
* schizophrenia
* autism spectrum disorder
Collection of hair follicle cells
study of the transmission of genetic variants
the genetic variants of interest will be investigated by sequencing or genotyping on genomic DNA
Relatives
Relatives of enrolled patients suffering from psychiatric disorder.
* test to detect psychiatric disorders
* blood or saliva sampling for genomic DNA extraction
* Collection of hair follicle cells
study of the transmission of genetic variants
the genetic variants of interest will be investigated by sequencing or genotyping on genomic DNA
Interventions
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study of the transmission of genetic variants
the genetic variants of interest will be investigated by sequencing or genotyping on genomic DNA
Eligibility Criteria
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Inclusion Criteria
* Subjects suffering from (according to DSM IV criteria) : Bipolar disorder, Unipolar depression, Schizophrenia, Autism spectrum disorder
* Age over 18 years
* Subject affiliated to the social security system
* Including patients under guardianship, curatorship,
* Patients included in the Fondation FondaMental cohort whose genetic analyses have revealed the need for comparative and functional genetic studies.
* Having signed the consent form
For relatives :
* Age over 18 years
* Relative of patient included in the Fondattion FondaMental cohort
* Including relative under guardianship, curatorship
* Having signed the consent
* Affiliated to social security
Exclusion Criteria
* Any condition that, in the opinion of the investigator, would make the subject's participation in the study undesirable or that would compromise compliance with the protocol
* Persons deprived of liberty
* Inability to understand French
18 Years
ALL
Yes
Sponsors
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Fondation FondaMental
OTHER
Responsible Party
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Principal Investigators
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Marion Leboyer, MD PhD
Role: STUDY_CHAIR
Fondation FondaMental
Stephane JAMAIN, PhD
Role: STUDY_DIRECTOR
Institut National de la Santé Et de la Recherche Médicale, France
Locations
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Hopital Albert Chenevier
Créteil, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2021-A02551-40
Identifier Type: OTHER
Identifier Source: secondary_id
FF21-GENI
Identifier Type: -
Identifier Source: org_study_id
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