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MRI Study of Subjects with ASD, Their Relatives and TD

Magnetic Resonance Imaging Neuroanatomical Study of Patients with an Autism Spectrum Disorder, Their Relatives and Typically Developing Subjects.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05470088
Enrollment
1000
Registered
2022-07-22
Start date
2022-03-13
Completion date
2039-09-13
Last updated
2025-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Autism Spectrum Disorder

Keywords

neuroimaging, mri, phenotype, heritability, genes

Brief summary

This project is structured around a central study called Study of genetic factors involved in autism and related conditions (Genes and Autism study, sponsor: INSERM). This study explores clinical and genetic aspects of ASD (autism spectrum disorders) and is complemented with several ancillary studies (such as this one) which will use the data of the main study and will allow an extensive review of phenotypes associated with ASD. In this ancillary study, we will go on the acquisition of anatomical, diffusion and functional MRI in subjects with ASD, relatives and controls. Our group has already performed several neuroanatomical studies of ASD. IWe recruited since 2010 more than 600 subjects (proponents, relatives and controls) to better understand the implication of brain abnormalities in ASD. This study involves specialized teams in neuroiamging based at INSERM, NeuroSpin (CEA), Robert Debré Hospital (APHP) and Pasteur Institute Our main objective is to identify structural, connectivity and functional peculiarities in subjects with ASD Secondary objectives include: * the identification of familial heritability patterns of ASD * correlate data obtained in brain imaging with genetic data * assess specificity and statistical reproducibility of the obtained results

Interventions

OTHERNeuroimaging (MRI)

Multimodal magnetic resonance imaging

Sponsors

APHP
CollaboratorOTHER
Institut Pasteur
CollaboratorINDUSTRY
Commissariat A L'energie Atomique
CollaboratorOTHER_GOV
Institut National de la Santé Et de la Recherche Médicale, France
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
24 Months to No maximum
Healthy volunteers
Yes

Inclusion criteria

* for patients: * being included in the main study C16-89 - Study of genetic factors involved in ASD and related disorders * having an ASD fulfilling DSM-5 diagnostic criteria (APA, 2012). Diagnosis will be done by a clinical expert, with the support of structured instruments (ADI-R, ADOS-2) * having at least 24 Months * being affiliated with the French health insurance * having signed the informed consent (by proposant or by legal tutors if the subject is \<18 or under legal custody) * for relatives * being included in the main study C16-89 - Study of genetic factors involved in ASD and related disorders * having at least 24 Months * being affiliated with the French health insurance * having signed the informed consent (by proposant or by legal tutors if the subject is \<18 or under legal custody) * for controls * being included in the main study C16-89 - Study of genetic factors involved in ASD and related disorders * having at least 24 Months * being affiliated with the French health insurance * having signed the informed consent (by proposant or by legal tutors if the subject is \<18 or under legal custody) Non-inclusion criteria: * for all subjects * severe mental retardation (IQ\<35 or developmental age\<18 months) * medical condition (either psychiatric or physical) not compatible with an inclusion * MRI counter indication * Current pregnancy or breastfeeding, assessed by questionnaire * Not willing to be informed of a brain abnormality diagnosed with MRI * for the relatives \*discovery of non filiation during the genetic analyses * for controls * Neurological history (except mental retardation) * Personal history of (checked with DIGS for Adults, Diagnostic Interview for Genetic Studies, Numberger et coll., 1994, or Kiddie SADS, Kiddie Schedule for Disorders and Schizophrenia for School Age Children, Orvaschel et coll., 1982): schizophrenia, addiction, bipolar disorder, recurrent depression (\> 2 episodes lifetime), severe, not stabilized anxiety disorder, history of episodes of epilepsy, significant inflammatory disease of immunosuppressive medication

Exclusion criteria

* for patients: ASD diagnosis not confirmed by assessments after the inclusion * for all subjects: discovery of a counter indication to MRI during the exam (e.g. claustrophobia)

Design outcomes

Primary

MeasureTime frameDescription
3DT1 MRI derived variablesDay 0Cortical folding Cortical thickness Cortical surface Cortical, white matter and subcortical volumes
Resting state fMRI derived variablesDay 0Whole-brain BOLD signal correlations
Task based fMRI derived variablesDay 0BOLD activation signals BOLD signal correlations
Diffusion MRI derived variablesDay 0Fractional anisotropy and mean diffusivity NODDI derived variables
quantitative T1 and quantitative T2 MRIDay 0Myelin Water Fraction

Countries

France

Contacts

Primary ContactRichard Delorme, M.D, Ph.D
richard.delorme@aphp.fr+33140032002
Backup ContactJosselin Houenou, M.D, Ph.D
josselin.houenou@inserm.fr+33149813051

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026