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Blood-brain Barrier Leakage in Dementia. A Dynamic Contrast-enhanced MRI Study

Sponsor
Maastricht University Medical Center (Other)
Overall Status
Unknown status
CT.gov ID
NCT02018913
Collaborator
Netherlands Alzheimer Foundation (Other)
140
Enrollment
48
Duration (Months)

Study Details

Study Description

Brief Summary

Alzheimer's disease (AD) and vascular dementia (VaD) are the most common forms of dementia. Yet, the cause of these diseases is still unknown. A potentially important initiating factor is a disrupted blood-brain barrier. This can initiate cerebral microangiopathy, which has frequently been associated with VaD. Nevertheless, also in most AD patients a substantial increase of vascular damage has been observed. The present study investigates the correlation between blood-brain-barrier breakdown and cognitive decline in AD and VaD. An innovative dynamic contrast-enhanced MRI scan that has recently been developed and tested at our institute, will be used to measure blood-brain barrier permeability.

Objective: We will investigate the relationship between this permeability measure and (i) cognitive performance and (ii) the status of MRI visible cerebrovascular pathology (i.e. white matter hyperintensities, lacunar infarctions, microbleeds) in the most common forms of dementia.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    140 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Study Start Date :
    Apr 1, 2014
    Anticipated Primary Completion Date :
    Apr 1, 2018
    Anticipated Study Completion Date :
    Apr 1, 2018

    Outcome Measures

    Primary Outcome Measures

    1. Blood brain barrier permeability as measured by T1-weighted dynamic contrast MRI [Up to 4 years: April 2014-April 2018]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    55 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    Patients:

    • Informed consent before participation in the study

    • Age of 55 and older

    • Diagnosed with AD, VaD, mixed AD and VaD, mild cognitive impairment, vascular cognitive impairment and subjective cognitive impairment

    • MMSE ≥ 20 and patients are mentally competent (in general, individuals with an MMSE ≥18 are considered mentally competent)

    Healthy participants:

    • Informed consent before participation in the study

    • Age of 55 and older

    • No Diagnosis of dementia, prodromal dementia, or mild cognitive impairment.

    • MMSE ≥ 26

    • No substantial memory complaints (according to participant)

    • Average age, gender and education is similar to the patient groups.

    Exclusion Criteria:

    • Contraindications for scanning (e.g. brain surgery, cardiac pacemaker, metal implants, claustrophobia, large body tattoos)

    • Contraindications for contrast agent Gadovist (renal failure) as determined by the estimated Glomular Filtration Rate eGFR < 30 mL/min; or known allergy to Gadovist. If participants have a low renal function as determined by <30 GFR <60, the PI will contact a radiologist (Paul Hofman). The radiologist will decide if this patient should be excluded.

    • Major vascular disorders (e.g. stroke, heart disease)

    • Psychiatric or neurological disorders: Major depression (< 12 months); history of schizophrenia; bipolar disorder; psychotic disorder NOS or treatment for a psychotic disorder (< 12 mnd); cognitive impairment due to alcohol abuse; epilepsy; Parkinson's disease; MS; brain surgery; brain trauma; electroshock therapy; kidney dialysis; Meniere's disease; and brain infections.

    • Structural abnormalities of the brain

    • Cognitive impairment due to alcohol/drug abuse or abuse of other substances.

    • Absence of reliable informant (for patient groups)

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Maastricht University Medical Center
    • Netherlands Alzheimer Foundation

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    F.R.J.Verhey, Professor of neuropsychiatry and old age psychiatry, Maastricht University Medical Center
    ClinicalTrials.gov Identifier:
    NCT02018913
    Other Study ID Numbers:
    • NL46089.068.13
    First Posted:
    Dec 23, 2013
    Last Update Posted:
    Dec 23, 2013
    Last Verified:
    Dec 1, 2013
    Additional relevant MeSH terms:
    Alzheimer Disease
    Dementia
    Dementia, Vascular

    Study Results

    No Results Posted as of Dec 23, 2013