Alzheimer Disease Dementia
Conditions
Interventions
None listed
Sponsors
Universitair Medisch Centrum Utrecht
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Participant of *parelsnoer neurodegeneratieve ziekten* project and diagnosed with (possible) Alzheimer's disease.;For parelsnoer: referred to memory clinic subjective and/or objective cognitive impairment CDR 0, 0.5 or 1 MMSE 20 or higher
Exclusion criteria
Exclusion criteria: Normal pressure Hydrocephalus, M. Huntington Recent CVA (
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The prevalence and total number of microinfarcts at 7T The prevalence and total number of microbleeds at 7T For the parelsnoer project participants will already receive a full clinical assessment, neuropsychological tests and a 3T MRI. Participants in the present study will also undergo some additional neuropsychological tests and a 7T MRI. | — |
Secondary
| Measure | Time frame |
|---|---|
| • Conventional brain MRI markers of AD (atrophy) and vascular lesions (large infarcts, white matter hyperintensities) at 3T MRI • Cognitive profile • Vascular risk factor profile | — |
Countries
Netherlands
Outcome results
None listed