Assessment of microglial activation in patients with schizophrenia stratified for C4 complement by PET using [18F]DPA-714
- Conditions
- pathology studied is schizophreniaMedDRA version: 20.0Level: PTClassification code: 10039626Term: Schizophrenia Class: 100000004873Therapeutic area: Diseases [C] - Pathological Conditions, Signs and Symptoms [C23]Therapeutic area: Psychiatry and Psychology [F] - Mental Disorders [F03]Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Investigative Techniques [E05]
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 75
Male or Female, aged from 18 to 55, patients with schizophrenia diagnostic according to DSM-5 and presenting HLA 8.1 AH haplotype (8.1 AH+) or presenting no HLA 8.1 AH haplotype ( (8.1 AH-), Male or Female healthy controls aged from 18 to 55 matched regarding age, sex, HLA/C4 according to patients (8.1 AH+ or 8.1 AH-)., Having Efficient Contraception for women of reproductive age ( contraception will be considered effective from the moment the patient declares the use of an oral contraceptive, the presence of an IUD other than copper ones, a diaphragm or a contraceptive implant, or the completion of a tubal ligation or sterilization by Essure process), Be able to understand research objectives and procedures, Be affiliated with or be a beneficiary of a social security scheme, Genetic criterion: TSPO genotype allowing tracer fixation (90% of subjects), Have signed a free and informed consent
Progressive chronic inflammatory disease (rheumatic, digestive, autoimmune), Adult subject to legal protection (guardianship of a tutor, or safeguard of justice), For healthy volunteers only : Pathology or history of Axis 1 psychiatric pathology investigated by the validated French version of the MINI (Mini International Neuropsychiatric Interview) questionnaire, Known hypersensitivity to radiopharmaceutical ([18F]DPA-714 or one of the excipients), History of severe renal or liver failure, Contraindication to MRI : pacemaker or neurosensory pacemaker or implantable defibrillator; clip on an aneurysm or clip on a vascular malformation of the brain; ferromagnetic intraocular or cerebral foreign body; prosthesis or ferro-metallic objects or fragments mobilizable magnetic; cochlear implants; peripheral stimulator; ventriculoperitoneal neurosurgical bypass valves; permanent eye or lip makeup. Automatic injection device type insulin pump, blood glucose sensor, Claustrophobia, Current pregnancy, breastfeeding, Person refusing to be informed of a significant health finding discovered in the research, Participation in research or management of a pathology with ionizing radiation exposure as part of a nuclear medicine examination (PET, SPECT, NM) in the year prior to or during the exclusion period of another research, Person deprived of liberty by administrative or judicial decision
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method