Overview

Patients with Alzheimer's disease and with early onset of symptoms (<65 years) (AD-Y) have a multi-domain cognitive deficit, whereas memory disorders (typical of the elderly patient's AD) are less often in the foreground. In addition, some MA-J have an atypical phenotype indicating focal brain damage, although they have the same pathological lesions: amyloid deposits and tau protein deposition (DNF). This is the case of posterior cortical atrophy (PCA) characterized by complex visual disturbances and atrophy affecting the more posterior regions of the brain. Based on the clinical profile of PCA patients, a more refined anatomo-clinical classification was proposed, distinguishing a rather "ventral" form and a rather "dorsal" form. The recent arrival of tau-specific PET tracers now makes it possible to evaluate in vivo fibrillary neurodegeneration (FND), which is well correlated with the severity of cognitive disorders. Advances in MRI have shown that each neurodegenerative syndrome targets a large-scale neural network, which in turn shows a vulnerability for a specific biological disease. In the case of AD, the reason for such a difference in cognitive and anatomical impairment between patients with diffuse involvement and others with more focal involvement is not known. One possible explanation is the existence, in focal forms, of neuronal mechanisms that oppose vulnerability. These mechanisms may correspond to the so-called "resilience" phenomenon, defined as resistance to a neuropathological process by the ability to optimize cognitive performance via the efficient recruitment of neural networks. The mechanisms underlying resilience in neurodegeneration are unknown. Their identification is very important for the management and treatment of AD.

Eligibility

Inclusion Criteria:

1. For all subjects:
   • Affiliation to a social security insurance or beneficiary
   • Informed consent form signed by the participant or his / her legal representative
   • Participants aged 40 to 80 years.
2. Selection of AD-Y group
   • In vivo proof of Alzheimer's pathology:
   • Determination of specific proteins on the cerebrospinal fluid (CSF, a routine care procedure). The values considered pathological (AD) are Aβ1-42 peptide <500 (μg / ml), and / or tau protein> 450 and phosphorylated tau protein> 60, IATI index <1, tau / Aβ protein ratios > 1.23 as well as phosphorylated tau protein / Aβ1-42> 0.211.
   • And / or a positive PET-amyloid imaging test.
   • Early-onset episodic memory deficit (<65 years), progressive onset with evidence of hippocampal amnesic syndrome at neuropsychological assessment.

     In memory tests, the amnesic hippocampal syndrome is defined by: a deficit of the
     free recall despite a reinforced encoding, an effectiveness of the indexing or an
     impairment of the recognition capabilities, the presence of intrusions. The presence
     during the tests of false memories spontaneous (intrusions) or provoked (false
     recognitions) is also very contributive to the definition of amnesic syndrome of the
     hippocampal type.

3. PCA group selection

Patients with a clinical and cognitive profile suggestive of PCA, characterized by:

• an in vivo proof of the Alzheimer pathology (see selection of the AD-Y group)
• a specific impairment of neuro-visual abilities, in the absence of major disorders of episodic memory (hippocampal) and executive functions.

Two possible variants:

• occipito-temporal variant: visuo-perceptive deficit in the foreground, early onset and progressive worsening; lack of visual identification of objects, symbols, words or faces;
• biparietal variant: visuospatial deficit in the foreground, early settlement and progressive worsening; Gerstmann syndrome; Balint syndrome; gestural apraxia; visual-spatial neglect. 4. Selection of the control subjects group
• Normal neurological and neuropsychological examinations.
• Control subjects will be matched in age to patients.

Non-inclusion Criteria:

1. General non-inclusion criteria:
   • Medical history of torsade de pointe or risk of torsade de pointes
   • Patient treated with drugs known to lengthen QT (see www.crediblemeds.org)
   • Contraindication to radiopharmaceutical injection:

     For precautions of safety of use of the radiopharmaceutical, a blood sample allowing
     to check the renal and hepatic functions will be realized before imagery. The delay
     between the sampling and the neuroimaging visit is left to the investigator's
     discretion based on the patient's biological results. In particular, the glomerular
     filtration rate will be calculated from the results obtained.
     In the event of renal insufficiency (GFR 30mL / min / 1.73m2), hepatic insufficiency
     or any other biological anomaly of grade 3 or higher detected during these analyzes,
     the participant will not be able to carry out PET imaging. In this case, the results
     of the analyzes will be sent to the doctor indicated by the participant. This
     evaluation, which involves a determination of serum creatinine, is part of the
     standard routine biological assessment performed in the context of cognitive
     disorders
     Inability to provide informed consent by participant or legal representative:
       -  Patient deprived of liberty by decision of justice or not benefiting from
          social cover.
       -  Person in the process of participating in another therapeutic research or in a
          period of exclusion from another research.
       -  Participants with a contraindication to MRI: pacemaker or cardiac
          defibrillator, implanted equipment activated by an electrical, magnetic or
          mechanical system, haemostatic clips of intracerebral aneurysms or carotid
          arteries , carriers of orthopedic implants.
       -  Contraindication to radiopharmaceutical injection: known hypersensitivity to
          the active substance or to any of the excipients, renal impairment (GFR 30mL /
          min / 1.73m2), hepatic insufficiency or any other biological abnormality of
          grade 3 or higher
       -  Person suffering from claustrophobia.
       -  Pregnancy (for women of childbearing age, a urine pregnancy test will be
          performed on the day of the inclusion visit and the PET-MRI examination).
       -  Any symptoms or biological values suggestive of a systemic disorder (renal,
          hepatic, cardiovascular, pulmonary) or any other medical conditions that could
          interfere with the interpretation of test results or compromise the health of
          patients.
       -  Person subject to a legal safeguard.

2. Specific non-inclusion criteria for AD-Y and PCA patients:

• Sudden appearance of cognitive deficits.
• Gait disturbances, convulsions, major behavior modification.
• Focal alterations to neurological examination, extrapyramidal signs, hallucinations, fluctuations. cognitive.
• Psychiatric, cerebrovascular, metabolic, inflammatory pathology. 3. Specific non-inclusion criteria for control subjects:
• Pathological neurological examination
• History of neurological disease (in particular ischemic stroke or neurodegenerative disease) or psychiatric illness (particularly severe depression, psychosis, or bipolar illness still requiring drug treatment at the time of inclusion)
• Physical affection that is serious or can interfere with cognitive functions.