cognitive impairment Dementia
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients: - Fulfilling the diagnostic criteria for subjective cognitive decline (SCD), mild cognitive impairment (MCI) due to AD or probable Alzheimer's disease (AD) - At least 50 years of age - Received an or a planned 18F-AV1451 PET in the context of the LUNAR, TRT AV-1451 or TITAN projects - Known amyloid status, Controls: age 20-30 years
Exclusion criteria
Exclusion criteria: Patients: - Cardiac pacemakers, ICD's and other introcorporeal devices interfering with MEG-signals - Severe claustrophobia - Specific exclusion criteria for 18F-AV1451 PET scanning or MRI scanning excluding patients from participation in the TITAN, LUNAR and TRT AV-1451 studies automatically disqualifies patients from participation in MANTA. , Controls: - Current cognitive, neurological or psychiatric disorders - Use of psychoactive medication - Contra-indications for MRI scanning - (Dental) implants, braces, cardiac pacemakers and ICD's interfering with MEG-signals - Severe claustrophobia - Current or planned pregnancy (both oral (telephone interview) and written (informed consent form) confirmation from participant).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| MEG endpoints 1) Primary MEG endpoints are: - relative theta power (4-8- Hz) of the target regions - normalized directed connectivity of the target regions (lower alpha band, 8 * 10 Hz) - betweenness centrality of the target regions (lower alpha band, 8 * 10 Hz) - path length between source and target region (lower alpha band, 8 * 10 Hz) 18F-AV1451 PET scan endpoints 1) the amount of specific 18F-AV1451 binding in each of the 90 regions of the AAL-atlas | — |
Secondary
| Measure | Time frame |
|---|---|
| MEG endpoints 2) Secondary MEG endpoints are: 2.1) all other frequency specific MEG endpoints 2.2) modularity analyses 2.3) multiplex network analyses | — |
Countries
Netherlands