[en] [18F]UCB-H is a fluorine-18 radiolabelled PET imaging tracer with a high affinity for the synaptic vesicle protein 2A (SV2A). This protein, involved in vesicle trafficking and widely distributed in the brain, represents the binding site and the primary mechanism of the antiepileptic drug levetiracetam. Levetiracetam has recently been suggested to reduce synaptic deficits in a mouse Alzheimer’s disease model and to improve cognition in patients with amnestic mild cognitive impairment, suggesting a possible role for this protein in synaptic integrity. The objective of this study was to investigate the cerebral distribution of [18F]UCB-H in healthy human volunteers. Dynamic PET imaging of the head of four healthy volunteers was performed over 100 minutes after injection of 170.4 ± 24.9 MBq of GMP produced [18F]UCB-H. The input function was acquired by arterial blood sampling during the dynamic PET acquisition. Blood data analysis showed a consistent tracer amount in whole blood and plasma indicating a very low degree of binding of the tracer to the red blood cells. Unchanged [18F]UCB-H fraction in plasma follows a bi-exponential behavioral decrease with a starting fraction of 92% of the injected amount of the tracer, measured at 3 min post injection. This fraction decreases to about 50% at 10 min post injection. The [18F]UCB-H PET data revealed a high and rapid uptake in the grey matter structures, matching the known ubiquitous distribution of SV2A in the brain. The kinetics of the tracer in the brain was characterized by an initial high uptake phase followed by rapid washout allowing the standard compartmental modeling (1-tissue compartment, 2-tissue compartment, and Logan graphical analysis). The three models gave consistent results. The two-tissue compartment model fitted the experimental data best and provided a total distribution volume of [18F]UCB-H in the brain greater than 7 mL/cm3 and a specific distribution volume around 3 mL/cm3. Our results indicate that [18F]UCB-H is a new radiotracer for brain SV2A proteins suitable for human studies. Further studies are warranted to assess SV2A modifications in neurological pathologies such as Alzheimer’s disease.
Disciplines :
Radiology, nuclear medicine & imaging
Author, co-author :
Bahri, Mohamed Ali ; Université de Liège - ULiège > Centre de recherches du cyclotron
Bastin, Christine ; Université de Liège - ULiège > Département des sciences cliniques > Neuroimagerie des troubles de la mémoire et révalid. cogn.
Aerts, Joël ; Université de Liège - ULiège > Centre de recherches du cyclotron
Bretin, Florian ; Université de Liège - ULiège > Centre de recherches du cyclotron
Warnock, Geoffery
Buchanan, Tim; UCB Pharma
Mella, Christine ; Université de Liège - ULiège > Centre de recherches du cyclotron
Mestdagh, Nathalie; UCB Pharma
Otoul, Christian; UCB Pharma
Koester, Franz; UCB Pharma
Valade, Anne; UCB Pharma
Mercier, Joël; UCB Pharma
Lemaire, Christian ; Université de Liège - ULiège > Centre de recherches du cyclotron
Mievis, Frédéric ; Université de Liège - ULiège > Centre de recherches du cyclotron
Léonard, Marc
Seret, Alain ; Université de Liège - ULiège > Département de physique > Imagerie médicale expérimentale
Luxen, André ; Université de Liège - ULiège > Département de chimie (sciences) > Laboratoire de chimie organique de synthèse
Plenevaux, Alain ; Université de Liège - ULiège > Centre de recherches du cyclotron
Salmon, Eric ; Université de Liège - ULiège > Département des sciences cliniques > Neuroimagerie des troubles de la mémoire et révalid. cogn.