Abstract
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Objectives [18F]FE-PE2I is a novel PET radioligand for imaging of the dopamine transporter (DAT). Noninvasive methods for DAT quantification using [18F]FE-PE2I rely on dynamic acquisitions, but a simplified protocol is preferable in a clinical setting. The aim of the study was to identify an optimal acquisition time window for simplified DAT quantification using [18F]FE-PE2I in control subjects (CS) and Parkinson’s disease (PD) patients.
Methods 10 CS and 10 PD patients were examined with [18F]FE-PE2I (HRRT, 93 min). ROIs for caudate (CAU), putamen (PUT), ventral striatum (VS), substantia nigra (SN) and cerebellum (CER) were drawn on co-registered MRI. Binding potentials (BPND) were obtained using wavelet-aided parametric imaging (WAPI), and specific binding ratios (SBR) were calculated using several time intervals, with CER as reference region. The time window that resulted in the highest correlation between BPND and SBR was used to create a mean image on which new SBR values were calculated. Effect sizes of SBR and BPND were calculated to assess differences between CS and PD patients.
Results The SBR values that correlated best to BPND were obtained for the time window between 16.5 and 42 min. A significant correlation between BPND and SBR was observed for CS (R2 =0.96) and PD patients (R2= 0.98). In the striatum, SBR values underestimated BPND by 18%±2% in CS and by 11%±4% in PD patients. In the SN, SBR overestimated BPND by 5% in CS and by 11% in PD patients. Similar effect sizes for BPND and SBR were found in CAU (both 0.6), PUT (1.7 and 1.5), VS (both 0.7), and SN (0.5 and 0.4).
Conclusions The optimal acquisition time window for simplified DAT quantification using [18F]FE-PE2I is between 16.5 and 42 min. Despite underestimation of BPND in high density regions, the SBR can be viewed as a valid quantification method for DAT using [18F]FE-PE2I, since it provides similar differentiation as BPND between CS and PD patients.
Research Support Swedish Foundation for Strategic Research