Molecular Neuroimaging of Neuroinflammation in Neurodegenerative Dementias

NCT ID: NCT02945774

Last Updated: 2025-03-05

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-08-31
• Study Completion Date: 2029-08-31

Brief Summary

Neuroinflammation is increasingly implicated as a potential critical pathogenic mechanism in a variety of neurologic and psychiatric disorders. This study will use hybrid PET/MRI imaging to evaluate neuroinflammation and its relationship to cerebral perfusion in frontotemporal dementia (FTD). Patients with FTD will be recruited from the Cognitive Neurology and Aging Brain clinics at Parkwood Institute and will undergo neurocognitive assessment and MRI/PET using the PET ligand FEPPA which binds to activated microglia, a marker of neuroinflammation. Correlations will be conducted to determine whether abnormal neuroinflammation is present in Frontotemporal dementia and whether differential patterns of neuroinflammation are present in different FTD clinical and molecular subtypes, and to determine the relationship between neuroinflammation, cerebral perfusion using arterial spin labeling MRI imaging techniques, and indices of brain structure including volumetric and white matter analysis.

Conditions

Frontotemporal Dementia

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

(18F)-FEPPA

Group Type: EXPERIMENTAL

(18F)-FEPPA

Intervention Type: RADIATION

PET ligand that binds to activated microglia, a marker of neuroinflammation

Interventions

(18F)-FEPPA

PET ligand that binds to activated microglia, a marker of neuroinflammation

Intervention Type: RADIATION

Eligibility Criteria

Inclusion Criteria

1. Patients diagnosed with a probable Frontotemporal Dementia or neurologically healthy control participants with no history of neurological problems

2. Study partner is available who has frequent contact with the subject and can accompany the subject to all clinic visits for the duration of the protocol.

3. Visual and auditory acuity adequate for neuropsychological testing

4. Good general health with no diseases expected to interfere with the study.

5. Subject is not pregnant, lactating, or of childbearing potential (i.e. women must be two years post-menopausal, surgically sterile or practicing an effective form of family planning

6. Willing to participate in a longitudinal imaging study at 12 months.

7. Willing to undergo MRI (3Tesla)/ PET scan (with FEPPA ligand) and no medical contraindications to MRI.

Exclusion Criteria

1. Any significant neurologic disease other than suspected Frontotemporal Dementia that would better account for symptoms (i.e. frontal lobe stroke).

2. Screening/baseline MRI scans with evidence of infection, infarction, or other focal lesions. Subjects with multiple lacunes are excluded.

3. Presence of pacemakers, aneurysm clips, artificial heart valves, ear implants, metal fragments or foreign objects in the eyes, skin or body that may preclude MRI participation as per MRI screening form.

4. Major depression, bipolar disorder as described in DSM-IV within the past 1 year. Psychotic features, agitation or behavioral problems within the last 3 months which could lead to difficulty complying with the protocol.

5. History of schizophrenia (DSM IV criteria).

6. Any significant systemic illness or unstable medical condition which could lead to difficulty complying with the protocol.

7. Clinically significant abnormalities in B12, or thyroid function tests that might interfere with the study.

8. Investigational agents are prohibited one month prior to entry and for the duration of the trial.

9. Exclusion for FEPPA: Current or recent participation in any procedures involving radioactive agents such that the total radiation dose exposure to the subject in any given year would exceed the limits of annual and total dose commitment set forth. The current regulation for radiation dose to patient volunteers and health control volunteers are contained within Health Canada's recently amended (June 19, 2012) Regulations Amending the Food and Drug Regulations (Positron-emitting Radiopharmaceuticals). Limitations for effective total body dose is 50 mSv (C.03.305 (c)) which has been increased from the previous values of 20 mSv (Table 1 in INFO-0491).

• Minimum Eligible Age: 30 Years
• Maximum Eligible Age: 95 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Parkwood Institute

London, Ontario, Canada

Site Status: RECRUITING

Countries

Canada

Central Contacts

S Jesso, BA

Role: CONTACT

cognitiveneurology@sjhc.london.on.ca

519-646-6000

Facility Contacts

S Jesso, BA

Role: primary

519-646-6000

Other Identifiers

107561

Identifier Type: -

Identifier Source: org_study_id