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Glutamatergic transmission exploration using PET (Positron Emission Tomography) imaging in autism compared to Fragile-X Syndrome ( FXS) and Healthy Volunteers
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| autistic patients | Experimental | [18F]FPEB PET imaging MRI (Magnetic Resonance Imaging) Biological samples |
|
| FXS patients | Experimental | [18F]FPEB PET imaging MRI Biological samples |
|
| Healthy subjects | Experimental | [18F]FPEB PET imaging MRI Biological samples |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| [18F]FPEB PET imaging | Drug | PET exam |
|
| Measure | Description | Time Frame |
|---|---|---|
| cerebral glutaminergic activity assessed by binding potential of [18F]FPEB | An average of 3 years |
| Measure | Description | Time Frame |
|---|---|---|
| distribution volume of [18F]FPEB | An average of 3 years |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU Tours | Tours | 37044 | France |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 33473111 | Result | Dupont AC, Serriere S, Barantin L, Vercouillie J, Tauber C, Gissot V, Bodard S, Chicheri G, Chalon S, Bonnet-Brilhault PF, Santiago-Ribeiro PM, Arlicot N. Study of influence of the glutamatergic concentration of [18F]FPEB binding to metabotropic glutamate receptor subtype 5 with N-acetylcysteine challenge in rats and SRM/PET study in human healthy volunteers. Transl Psychiatry. 2021 Jan 20;11(1):66. doi: 10.1038/s41398-020-01152-2. |
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There is no plan to share data.
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| ID | Term |
|---|---|
| D001321 | Autistic Disorder |
| D005600 | Fragile X Syndrome |
| ID | Term |
|---|---|
| D000067877 | Autism Spectrum Disorder |
| D002659 | Child Development Disorders, Pervasive |
| D065886 | Neurodevelopmental Disorders |
| D001523 | Mental Disorders |
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| Biological samples | Other | blood sample and urine sample |
|
| MRI | Other | MRI exam |
|
| D038901 | X-Linked Intellectual Disability |
| D008607 | Intellectual Disability |
| D019954 | Neurobehavioral Manifestations |
| D009461 | Neurologic Manifestations |
| D009422 | Nervous System Diseases |
| D025064 | Sex Chromosome Disorders |
| D025063 | Chromosome Disorders |
| D000013 | Congenital Abnormalities |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D030342 | Genetic Diseases, Inborn |
| D040181 | Genetic Diseases, X-Linked |
| D020271 | Heredodegenerative Disorders, Nervous System |