MEMENTO-VAScular COmponents of Dementia

NCT ID: NCT02264899

Last Updated: 2022-01-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

332 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-11-04

Study Completion Date

2021-10-29

Brief Summary

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A Multicenter national longitudinal cohort study including at least 800 individuals recruited from French Research Memory Centers and followed up over 36 months and included in Memento.

Detailed Description

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Alzheimer's disease (AD) is a neurodegenerative disorder thought to be caused by the accumulation of the peptide amyloid beta and the hyperphosphorylated tau protein in the brain. There are increasing arguments in favor of an important role of vascular damages in the development and progression of AD.

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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Alzheimer's Disease (AD) Alzheimer's Disease (AD) Related Disorders

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Alzheimer's disease and related disorders

Group Type EXPERIMENTAL

in Memento-VASCOD

Intervention Type OTHER

* 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

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Participants to MEMENTO-Vascod should be included in MEMENTO.
* 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

* Are under guardianship
* Live in skilled nursing facility
* Are Pregnant or breast feeding women
Minimum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ministry for Health and Solidarity, France

OTHER_GOV

Sponsor Role collaborator

University Hospital, Bordeaux

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

CHU de Bordeaux - Pellegrin

Bordeaux, , France

Site Status

CHU de Dijon

Dijon, , France

Site Status

CHU de Lille

Lille, , France

Site Status

Hospices civils de Lyon

Lyon, , France

Site Status

AP-HM

Marseille, , France

Site Status

CHU de Montpellier

Montpellier, , France

Site Status

AP-HP - Hôpital BROCA

Paris, , France

Site Status

AP-HP - Hôpital LARIBOISIERE

Paris, , France

Site Status

CHU de Strasbourg

Strasbourg, , France

Site Status

Countries

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France

Other Identifiers

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CHUBX 2012/32

Identifier Type: -

Identifier Source: org_study_id

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