Alzheimer's Disease
Conditions
Keywords
Alzheimer's Disease, MRI, PET
Brief summary
The aim of the study is to determine if regional cerebral blood flow, measured by dynamic arterial spin labeling (dASL), can be a biomarker for stage of Alzheimer's disease. The study is designed to be conducted in 2 parts in participants with mild to moderate Alzheimer's disease, and participants with normal cognition. Various imaging studies will be done using magnetic resonance imaging (MRI) and positron emission tomography (PET) along with neurocognitive assessments. Participants who meet the study-entry criteria will have up to 8 study visits. Repeat imaging studies may be required if the initial data are incomplete or un-interpretable. The maximum number of PET scans during the study will be limited to four.
Interventions
OTHERMRI
During the study all participants will have 4 total MRI scans: baseline, 1 week, 6 and 12 months.
OTHERFDG-PET
2 to 4 PET scans will be done over 12 months, 2 planned and 2 more if data from any of these are un-interpretable
Sponsors
Merck Sharp & Dohme LLC
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
The prospective participant must meet, at least, all of the criteria below (among others determined by the study staff) to be eligible for study participation. The participant: * Has mild-to-moderate Alzheimer's Disease (AD), OR is considered cognitively normal; * Has been on stable doses of any regularly used medications for 4 weeks prior to study start; * Must have been on a stable dose for 12 weeks prior to study start, of any medications taken for AD.
Exclusion criteria
If the prospective participant meets any of the criteria below (among others determined by the study staff) they will NOT be eligible for study participation. The participant: * Is living in a nursing home or skilled nursing facility; * Has severe AD; * Cannot undergo MRI; * Cannot undergo PET scans; * Has a history of neurological or neurodegenerative disorders, other than AD within 2 years prior to study start; * Has taken Tacrine or anti-parkinsonian medications within 3 months of study start; * Has taken corticosteroids, blood thinners, narcotic analgesics, benzodiazepines, or certain antihistamines within 1 month of study start; * Initiates, discontinues, or changes the dose of any AD treatment during the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Regional cerebral blood flow, as measured by dASL. | 1 week, 6 and 12 months | Part I: regional cerebral blood flow, measured by dASL at Baseline and 1 week in AD participants and cognitively normal controls. Part II: regional cerebral blood flow, measured at 6 months and 12 months in AD participants and normal control participants. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Rate of cerebral glucose consumption, MRglc, as measured by fludeoxyglucose-PET (FDG-PET) | 12 months | Regional cerebral rate of glucose consumption, MRglc, as assessed by FDG-PET will be measured at Baseline in (Part I) and at 12 months in (Part II), in AD participants and normal control participants. |
| Resting state functional MRI blood-oxygen-level-dependent (fMRI BOLD) response | 1 week, 6 and 12 months | The resting state fMRI BOLD (blood-oxygen-level-dependent) signal will be evaluated for 'Goodness-of-Fit' to the default mode network at Baseline, 1 week, and 6 and 12 months in AD participants and normal control participants. |
Outcome results
None listed