Imaging Synapses With [11C] UCB-J in the Human Brain
Start Date
8/1/2019
Completion Date
12/1/2025
Summary
The purpose of this study is to utilize the radioactive positron emission tomography (PET) tracer \[11C\]UCB-J to test the neural synaptic pruning hypothesis of schizophrenia. This imaging method allows for the quantification of synaptic density in the living human brain and has the unprecedented ability to directly examine the synaptic pathology underlying neuropsychiatric disease. The neural synaptic pruning hypothesis posits that a key pathogenic process of schizophrenia is the over-exuberant elimination of neural synapses during development. The confirmation of reduced synaptic density in schizophrenia as evidenced by \[11C\]UCB-J has the potential to lead to a number of ground-breaking clinical innovations, such as laboratory-based diagnostics and prognostics, and novel, disease-modifying treatments.
Eligibility Criteria
Age Range: 18 years to 65 years
Interventions
[11C]UCB-J radiotracer
PET-MR
Conditions
Locations
VA Palo Alto Health Care System
Palo Alto, California 94304
United States
Stanford University
Stanford, California 94305
United States