Finding the biological basis of lost brain connections in Alzheimer*s Disease
- Conditions
- Alzheimer's diseasemild cognitive impairment10029305
- Registration Number
- NL-OMON54226
- Lead Sponsor
- Vrije Universiteit Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 55
- Clinical diagnosis of mild cognitive impairment due to Alzheimer's Disease
- Abnormal CSF biomarker for aggregated amyloid
- Signed informed consent for Amsterdam Dementia Cohort (ADC) (P2016.061) and
Amsterdam Dementia Biobank (P2017.315)
- Age >=50 years
- No CSF collection or MRI-imaging at screening at memory clinic
- Clinical diagnosis of dementia or subjective cognitive decline
- Other neurological diagnosis, such as Parkinson*s disease, symptomatic
stroke, mental retardation, brain tumor or infection, likely to be cause of
cognitive impairment
- Major psychiatric disorder, such as psychosis, schizophrenia, depression with
vital signs, severe personality disorder, abuse of alcohol or other substances,
likely to be cause of cognitive impairment
- Use of (oral) anticoagulants or other contraindications for lumbar puncture
- Contraindications for MRI scan (e.g., metal implants, pacemaker)
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Main predictor: baseline and longitudinal biological processes measured with<br /><br>CSF proteomics.<br /><br>Main endpoints: decline in brain network measures over time compared to<br /><br>baseline.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary endpoints:<br /><br>- Decline in cognitive functioning over time compared to baseline as measured<br /><br>with a neuropsychological test battery<br /><br>- Progression to dementia</p><br>