Study Results
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Basic Information
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COMPLETED
NA
332 participants
INTERVENTIONAL
2014-11-04
2021-10-29
Brief Summary
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Detailed Description
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The time course of these vascular alterations and how they relate to dementia and AD pathology remain unclear, as no protocol that allows the development of the diverse vascular pathology to be scored, and hence to be tracked with ageing, has so far been developed and widely validated. The aims of this project are to investigate, in a large clinical sample of patients presenting either isolated cognitive complaints or light to mild cognitive deficits, how vascular risk factors and vascular alterations (assessed at macro and micro levels) relate to cerebrovascular disease and cognitive decline.
The primary objective of this ancillary study is to investigate the prospective association between vascular risk factors, inflammation markers and vascular damages on cognitive decline and neurodegeneration progression over up to 4 years of follow-up in a sample of individuals presenting with a spectrum of cognitive profiles ranging from isolated cognitive complaints to cognitive deficits without dementia.
The secondary objectives are the following
* To investigate the role of vascular risk factors (diabetes, hypertension, hypercholesterolemia) and vascular damages on progression to clinical dementia over up to 4-year follow-up.
* To study whether the interaction between changes in markers of macrovascular and microvascular structures on cognitive deficits progression.
* To study the association between in BP, hypertension, antihypertensive treatments and vascular damages, progression of cerebrovascular disease seen at MRI and cognitive decline and dementia risk
* To assess the temporality of vascular damages burden on neurodegeneration
* To assess the association between retinal vasculature defect and brain neurovascular damages
* To study the link between vascular damages and AD pathology (Cerebro-Spinal Fluid (CSF) and Positron emission tomography (TEP) amyloid imaging) biomarkers in the subsample of participants having all measures available
* To investigate how inflammatory markers mediate the association between vascular damages and neurodegeneration
* To assess whether vascular factors and neurodegenerative factors act independently or synergistically on the course of cognitive decline
* To assess simultaneously the impact of vascular damages on end organs (brain, eye, and kidney)
* To study the correlation between cerebral blood flow, measured by Arterial spin-Labeled (ASL) MRI and cognitive decline
* To study whether genetic polymorphisms revealed from genome-wide association studies (GWAS) of AD of vascular factors could modulate the association between vascular damages and cognitive decline
Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Alzheimer's disease and related disorders
in Memento-VASCOD
* Pulse wave velocity assessment
* Cerebral MRI including Arterial Spin Labeling (ASL) and Magnetic Resonance Angiography (MRA) sequences
* Ophthalmological exams: Spectral Domain-Optical Coherence Tomography (SD-OCT), colour photographs of the retina, visual acuity and axial lenght measurement
* Neuropsychological testing and behaviorial and mood scales
* Urinary albumin excretion measurement
Interventions
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in Memento-VASCOD
* Pulse wave velocity assessment
* Cerebral MRI including Arterial Spin Labeling (ASL) and Magnetic Resonance Angiography (MRA) sequences
* Ophthalmological exams: Spectral Domain-Optical Coherence Tomography (SD-OCT), colour photographs of the retina, visual acuity and axial lenght measurement
* Neuropsychological testing and behaviorial and mood scales
* Urinary albumin excretion measurement
Eligibility Criteria
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Inclusion Criteria
* To have signed a specific MEMENTO-Vascod informed consent form, prior to any Vascod ancillary study related procedures
* To be aged 50 years old and above
* To have a Clinical Dementia Rating scale \<0.5 and to be not demented;
Exclusion Criteria
* Live in skilled nursing facility
* Are Pregnant or breast feeding women
50 Years
ALL
No
Sponsors
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Ministry for Health and Solidarity, France
OTHER_GOV
University Hospital, Bordeaux
OTHER
Responsible Party
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Principal Investigators
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Genevieve CHENE, Prof
Role: PRINCIPAL_INVESTIGATOR
CIC-EC1401 - ISPED - CHU de Bodeaux
Geneviève CHENE, Prof
Role: STUDY_CHAIR
CIC-EC1401 - ISPED - CHU de Bordeaux
Carole DUFOUIL, Director
Role: STUDY_DIRECTOR
CIC-EC1401 - ISPED - CHU de Bordeaux
Locations
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CHU d'Amiens
Amiens, , France
CHU de Bordeaux - Pellegrin
Bordeaux, , France
CHU de Dijon
Dijon, , France
CHU de Lille
Lille, , France
Hospices civils de Lyon
Lyon, , France
AP-HM
Marseille, , France
CHU de Montpellier
Montpellier, , France
AP-HP - Hôpital BROCA
Paris, , France
AP-HP - Hôpital LARIBOISIERE
Paris, , France
CHU de Strasbourg
Strasbourg, , France
Countries
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Other Identifiers
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CHUBX 2012/32
Identifier Type: -
Identifier Source: org_study_id
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