Clarifying the Vascular Aspects of Dementia; Natural History Study

Status: Active_not_recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

Cerebral amyloid angiopathy (CAA), a common cerebrovascular small vessel disease (SVD), is a frequently (98%) found co-morbidity at autopsy in patients with Alzheimer's disease (AD). Current in vivo hallmarks of CAA represent changes relatively late in the disease process and leaves CAA in AD often undetected. Recently, it was shown that decreased vascular reactivity (VR) measured with blood oxygen level dependent (BOLD) MRI, after visual stimulus, is an early CAA marker. With BOLD-MRI to detect decreased VR in different stages of AD, it was shown that increasing stages of AD associate with decreasing VR independent of age, classic SVD markers and atrophy. Moreover, VR is associated with cognitive deficits. Therefore, cross-sectional data indicate that decreased VR is an important co-morbidity already in early stages of AD with an independent effect on disease severity. In this respect, the study aim is to determine the natural course of the decrease of VR in both controls and (early stage) AD patients to monitor AD disease progression. This is an essential step to aid in the development and application of effective treatment as it is expected that CAA can cause/worsen AD pathology.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Maximum Age: 90
Healthy Volunteers: t
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• For this study three different routes for inclusion exists. Inclusion criteria for each group separately are shown below.

‣ Participants who were included in our previous CASCADE study (P19.039).

• Capable of giving informed consent (see appendix)

⁃ Patients who attended a memory clinic within one year ago

• Diagnosed with (mixed) probable AD

∙ Diagnosed as MCI

∙ Diagnosed as SCI

∙ Age between 50-90 years

∙ Capable of giving informed consent (see appendix)

⁃ Control subjects

• Healthy adults without memory complaints

∙ Age between 50 -90 years

∙ Capable of giving informed consent

Locations
Other Locations
Netherlands
Leids Universitair Medisch Centrum
Leiden
Time Frame
Start Date: 2023-09-04
Completion Date: 2026-09
Participants
Target number of participants: 120
Treatments
Dementia patients
Patients with a dementia diagnosis; probable Alzheimer or mixed-type dementia
MCI patients
Patients with a MCI diagnosis; patients demonstrating cognitive deficits on neuropsychological testing but not fulfilling the criteria for dementia.
SCI patients
Patients not demonstrating cognitive deficits on neuropsychological testing are classified as SCI
Controls
Control subject without cognitive complaints
Sponsors
Leads: Leiden University Medical Center

This content was sourced from clinicaltrials.gov