Imaging Synaptic Density in Aging and Alzheimer Disease with [F]SynVesT-1.

Synaptic density imaging with PET is a relatively new approach to monitoring synaptic injury in neurodegenerative diseases. However, there are remaining technical and clinical questions, including questions on reference region selection and on how specific phenotypic presentations and symptoms of Alzheimer disease (AD) are reflected in alterations in synaptic density. Using a synaptic vesicle glycoprotein 2A (SV2A) PET ligand radiolabeled with the F isotope ([F]SynVesT-1), we performed sensitivity analyses to determine the optimal reference tissue modeling approach to derive whole-brain ratio images. Using these whole-brain images from a sample of young adults, older adults, and patients with varied phenotypic presentations of AD, we then contrasted regional SV2A density and in vivo AD biomarkers. Reference tissue optimization concluded that a cerebellar gray matter reference region is best for deriving whole-brain ratio images. Using these images, we found a strong inverse association between [F]SynVesT-1 PET uptake and amyloid β and tau PET deposition. Finally, we found that individuals with a lower temporal gray matter volume but higher temporal [F]SynVesT-1 PET uptake show preserved performance on the mini-mental state examination. [F]SynVesT-1 PET shows a close association with in vivo AD pathology, and preserved SV2A density may be a possible marker for resilience to neurodegeneration.