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About
The AETIONOMY project will generate a refined taxonomy and testable mechanisms underlying the derived stratification of patients.
Full description
The main objective of the AETIONOMY clinical study is to test in real clinical samples the validity of the hypothesized underlying pathogenic mechanisms of AD and PD.
Although not fully understood, the pathophysiology of neurodegenerative diseases results from the complex interplay between several biological pathways such as neuronal excitotoxicity, oxidative stress, protein miss-folding and aggregation, neuroinflammation, apoptosis etc. It is thus likely that the maps generated by the AETIONOMY project will comprise several distinct biological hypotheses and subgroups of patients defined by 1 or more of these hypotheses. The Consortium has insufficient resources to validate all these hypotheses. Although it is anticipated that the AETIONOMY Project will provide novelty in the investigators' understanding of neurodegenerative diseases, it is expected that previously known biological pathways will come out from the data mining approach, e.g. mitochondrial pathway for PD or beta-amyloid aggregation for AD. AETIONOMY project will take advantage of these previously known pathways that will be considered as internal controls. One or two novel pathogenic pathways will be tested in parallel. Overall, this strategy will allow validating two hypotheses for each neurodegenerative disease (AD and PD). As it cannot be predicted what hypotheses will precisely rise from the data mining, the approach must be adaptative. However, it is possible to anticipate which population, clinical data, brain imaging procedure, and which biological samples will have to be applied for their validation. The AETIONOMY clinical study thus aims at assembling a standardized clinical, brain imaging, and biological collection from AD patients, PD patients and healthy controls to validate the model proposed by the AETIONOMY project. The Consortium will identify potential pathogenic pathways (established and novel) involved in AD and PD and will deliver surrogate markers which serve as readouts of the involved pathways. The model will be considered validated if the selected makers allow subject stratification in the AETIONOMY clinical study according to what has been postulated in the model. Additional correlation between biomarker expression and brain imaging will be performed when available. A transversal cohort will be recruited from 4 sites in Europe (France, Germany, Spain, and Sweden), including AD and PD patients, individuals at risk of AD and PD, and healthy controls.
Approximately 655 subjects will be recruited. Subjects will have a single study visit with clinical assessments, biological sampling, brain imaging (AD group only). Standardized procedures will be used for biological sampling as well as for brain image acquisition.
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Inclusion and exclusion criteria
INCLUSION CRITERIA
FOR ALL
PARKINSON'S DISEASE GROUP
Idiopathic PD patients:
PD patients with mutation in Parkin, Leucine-rich repeat kinase 2 (LRRK2) or Glucosidase beta acid (GBA) gene:
Subjects at risk of PD:
Healthy control subjects:
ALZHEIMER'S DISEASE GROUP
Prodromal AD patients:
Age ≥ 50 to ≤ 80 years.
Study partner/caretaker has noticed a recent gradual decrease in the subject's memory (e.g. over the prior 12 months), which the subject may or may not be aware of.
Cognitive requirements:
CSF Aβ1-42 level ≤ 550 pg/mL as measured by the local laboratory (cut off may depend on the performing lab).
Subject or study partner has ability to provide written informed consent in accordance with ICH, GCP, and local regulations.
Each subject must have a study partner/caretaker who is reliable and competent. The study partner/caretaker must have a close relationship with the subject, have face to face contact at least 3 days/wk for a minimum of 6 waking hours/wk and be willing to accompany the subject to the study assessments.
Be able to read at a 6th grade level or equivalent, as determined by the investigator, and must have a history of academic achievement and/or employment sufficient to exclude mental retardation.
Have results of clinical laboratory tests (complete blood count [CBC], blood chemistries, thyroid stimulating hormone [TSH]) within normal limits or clinically acceptable to the site principal investigator at screening.
Have results of a physical examination, vital signs, and electrocardiogram (ECG) within normal limits or clinically acceptable to the site principal investigator at screening.
Preclinical AD patients (asymptomatic at risk of AD):
Healthy control subjects:
EXCLUSION CRITERIA
FOR ALL
Any of the following medications within 1 week prior to inclusion:
Vaccination with live vaccines within 3 weeks and/or with inactivated vaccines within 2 weeks prior to inclusion
On-going viral or bacterial infection requiring at least symptomatic treatment, or antibiotics, or associated with fever or pain.
Any psychiatric condition, which in the opinion of the investigator might preclude participation.
Any lab abnormality, which in the opinion of the investigator might preclude participation.
Pregnant woman or lactating or planning pregnancy during the course of the study (Includes a negative urine pregnancy test or to be of non-child bearing potential).
Participant who does not wish to be informed of any clinically relevant abnormalities (as determined by the investigator at that site) identified during the course of the study (For France only).
PARKINSON'S DISEASE GROUP
Idiopathic PD patients:
PD patients with mutation in Parkin, LRRK2 or GBA gene:
Subjects at risk of PD:
PD Healthy control subjects:
ALZHEIMER'S DISEASE GROUP
Prodromal AD patients:
Rosen-modified Hachinski Ischemia Score > 4 at screening (ie, evidence of vascular dementia).
Known history of stroke or evidence from MRI scan that is clinically important in the investigator's opinion.
Evidence of a clinically relevant neurological disorder other than the disease being studied (ie, probable AD), including but not limited to: vascular dementia, parkinsonism, frontotemporal dementia, Huntington's disease, amyotrophic lateral sclerosis, multiple sclerosis, progressive supranuclear palsy, neurosyphilis, dementia with Lewy bodies, other types of dementia, mental retardation, hypoxic cerebral damage, cognitive impairment due to other disorders, or head trauma with loss of consciousness that led to persistent cognitive deficits.
The subject has evidence of a clinically relevant or unstable psychiatric disorder, based on Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition - Text Revision (DSM-IV-TR) criteria,
Previous MRI scan showing evidence of a neurological disorder other than probable AD or > 4 cerebral microhemorrhages (regardless of their anatomical location or diagnostic characterization as "possible" or "definite"), a single area of superficial siderosis, evidence of a prior macrohemorrhage, 3 lacunar infarcts, any cortical infarct over 5 mm, or any other clinically significant finding (eg, brain tumor).
A recent or ongoing, uncontrolled, clinically significant medical condition within 3 months of the screening (such as, but not limited to, diabetes, hypertension, thyroid or endocrine disease congestive heart failure, angina, cardiac or gastrointestinal disease)
The subject has:
Contraindications for MRI scan (pacemaker, implanted cardioverter-defibrillator, neurostimulation system, cochlear implant, metallic foreign body (metal sliver) in the eye, metallic prosthesis, cerebral aneurysm clip, ventriculoperitoneal neurosurgical bypass valve, fixed dental prosthesis, known claustrophobia).
Contraindications for lumbar puncture: current treatment with anticoagulants (e.g., coumadin, heparin) or double antiaggregant therapy.
Preclinical AD patients (asymptomatic at risk of AD):
Rosen-modified Hachinski Ischemia Score > 4 at screening (ie, evidence of vascular dementia).
Known history of stroke or evidence from MRI scan that is clinically important in the investigator's opinion.
Evidence of a clinically relevant neurological disorder other than the disease being studied (ie, probable AD), including but not limited to: vascular dementia, parkinsonism, frontotemporal dementia, Huntington's disease, amyotrophic lateral sclerosis, multiple sclerosis, progressive supranuclear palsy, neurosyphilis, dementia with Lewy bodies, other types of dementia, mental retardation, hypoxic cerebral damage, cognitive impairment due to other disorders, or head trauma with loss of consciousness that led to persistent cognitive deficits.
The subject has evidence of a clinically relevant or unstable psychiatric disorder, based on DSM-IV-TR criteria,
Previous MRI scan showing evidence of a neurological disorder other than probable AD or > 4 cerebral microhemorrhages (regardless of their anatomical location or diagnostic characterization as "possible" or "definite"), a single area of superficial siderosis, evidence of a prior macrohemorrhage, 3 lacunar infarcts, any cortical infarct over 5 mm, or any other clinically significant finding (eg, brain tumor).
The subject has:
Contraindications for MRI scan (pacemaker, implanted cardioverter-defibrillator, neurostimulation system, cochlear implant, metallic foreign body (metal sliver) in the eye, metallic prosthesis, cerebral aneurysm clip, ventriculoperitoneal neurosurgical bypass valve, fixed dental prosthesis, known claustrophobia).
Contraindications for lumbar puncture: current treatment with anticoagulants (e.g., coumadin, heparin) or double antiaggregant therapy.
Under guardianship or curatorship.
AD Healthy control subjects:
220 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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