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KMID : 1148920140480040287
Nuclear Medicine and Molecular Imaging
2014 Volume.48 No. 4 p.287 ~ p.294
The Effect of SSRIs on the Binding of 18F-FP-CIT in Parkinson Patients: A Retrospective Case Control Study
Seo Min-Jung

Oh Min-Young
Cho Min-Jung
Chung Sun-Ju
Lee Chong-Sik
Kim Jae-Seung
Abstract
Purpose: 18F-FP-CIT [18F-fluorinated N-3-fluoropropyl-2-beta-carboxymethoxy-3-beta-(4-iodophenyl) nortropane] is useful for detecting striatal dopamine transporter (DAT). Since FP-CIT shows relatively high affinities for DAT and serotonin transporter (SERT), its binding can be influenced by selective serotonin reuptake inhibitors (SSRIs). We aimed to evaluate the effect of SSRIs on the binding of 18F-FP-CIT.

Methods: In our 18F-FP-CIT positron emission tomography (PET) data pool, images of 24 drug-naive Parkinson¡¯s disease (PD) patients (62.6?¡¾?10.6 years), 111 PD patients taking SSRIs [escitalopram (n?=?19) and fluvoxamine (n?=?20)] or clonazepam (n?=?72), and 10 normal people were reviewed. PET images acquired 3 h after 18F-FP-CIT injection were analyzed by an automated method using a predefined volume of interest (VOI) set of the striatum (ST), occipital cortex (OC), raphe nuclei (RN), and cerebellar cortex (CB). The uptake ratios (URs) of each VOI to the CB were compared among the groups.

Results: The ST/CB URs of all PD groups were significantly lower than that of normal group. When adjusted for drug severity, ST/CB URs were higher in drug-naive group but had no difference among antidepressant groups. Whereas OC/CB URs were not different among groups (p?>?0.05), RN/CB URs were significantly lower in SSRI groups than in non-SSRI groups (p?
Conclusions: PD patients taking SSRIs showed significantly decreased URs in the RN but not the OC. When adjusted for Hoehn and Yar (HY) score, ST URs were not different among antidepressant groups. This result suggests that the OC may be used as a reference region for the quantification of DAT binding in 18F-FP-CIT PET images of PD patients taking SSRIs.
KEYWORD
Parkinson¡¯s disease, Selective serotonin reuptake inhibitor, 18F-FP-CIT, PET
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