The University of Alabama at Birmingham (UAB) Neuroinflammation in Parkinson's Disease-TSPO- Positron Emission Tomography (PET) Substudy

Sponsor
University of Alabama at Birmingham (Other)
Overall Status
Recruiting
CT.gov ID
NCT03457493
Collaborator
(none)
20
1
2
74.3
0.3

Study Details

Study Description

Brief Summary

The primary objective of this substudy is to measure the concentration and the regional brain distribution of activated brain microglia/macrophages using the PET (Positron Emission Tomography) ligand Fluorodeoxyglucose dimethylpyrazolo ([18F]DPA-714) in participants enrolled in the UAB Neuroinflammation in Parkinsons Disease (PD) study. The PET tracer [18F]DPA-714 binds to the 18 kilodaltons (kDa) translocator protein (TSPO, also known as the peripheral benzodiazepine receptor) in the mitochondria of activated microglia/macrophages and provides a non-invasive measure of neuroinflammation. The amount and distribution of [18F]DPA-714 in the brain will be correlated to clinical data acquired through the separate ongoing Neuroinflammation in PD study. The primary objective of this study is to determine if patients with PD have higher levels of neuroinflammation than healthy controls as measured with [18F]DPA-714-PET/MRI.

Condition or Disease Intervention/Treatment Phase
Phase 1/Phase 2

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
UAB Neuroinflammation in Parkinson's Disease - TSPO-PET Substudy
Actual Study Start Date :
Mar 22, 2018
Anticipated Primary Completion Date :
Jun 1, 2024
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Healthy Controls, DPA-714-PET/MRI

Drug: DPA-714-PET/MRI
DPA-714-PET/MRI

Experimental: Early Parkinson's Disease, DPA-714-PET/MRI

Drug: DPA-714-PET/MRI
DPA-714-PET/MRI

Outcome Measures

Primary Outcome Measures

  1. Comparison of TSPO-PET measures of neuroinflammation between PD patients and healthy controls. [2 years]

    Estimates of brain TSPO concentrations measured with PET will serve as a marker for neuroinflammation. TSPO-PET measures will be compared between PD patients and healthy controls. We expect the PD patients to have higher measures of neuroinflammation than healthy controls.

  2. Correlation of DPA-714-PET/MRI with demographics, clinical and biospecimen assessments from Neuroinflammation in PD study [2 years]

    The estimates of neuroinflammation measured with TSPO-PET will be correlated with clinical assessments of PD severity and biospecimens collected through the UAB Neuroinflammation in PD study.

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Enrollment in the UAB Neuroinflammation in PD study under the separate UAB approved research protocol Institutional Review Board number (IRB)-300000690.

  2. Negative urine or serum Human chorionic gonadotropin (hCG) test within 2 days of [18F]DPA-714-PET administration in women of child bearing potential. Women who are post-menopausal with at least 1 year since last menses or documented surgical sterilization will not require pregnancy testing.

  3. High or mixed affinity binder for TSPO ligands based on genotyping for single nucleotide polymorphism (SNP) rs6971.

Exclusion Criteria:
  1. Meets any exclusion criteria for the UAB Neuroinflammation in PD study.

  2. Contraindication to MRI and/or PET imaging

  3. Inability to participate in the imaging studies due to severity of PD or other medical comorbidities.

  4. Low affinity binder for TSPO ligands based on genotyping for SNP rs6971. -

Contacts and Locations

Locations

Site City State Country Postal Code
1 UAB Advanced Imaging Facility Birmingham Alabama United States 35294

Sponsors and Collaborators

  • University of Alabama at Birmingham

Investigators

  • Principal Investigator: Jonathan McConathy, MD, University of Alabama at Birmingham

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jonathan E McConathy, Principal Investigator, University of Alabama at Birmingham
ClinicalTrials.gov Identifier:
NCT03457493
Other Study ID Numbers:
  • IRB-300001025
First Posted:
Mar 7, 2018
Last Update Posted:
Mar 31, 2022
Last Verified:
Mar 1, 2022
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 31, 2022