[18F]PR04.MZ PET/CT imaging for evaluation of nigrostriatal neuron integrity in patients with parkinson disease
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Juri Clavería, Carlos
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[18F]PR04.MZ PET/CT imaging for evaluation of nigrostriatal neuron integrity in patients with parkinson disease
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Abstract
Degeneration of dopaminergic, nigrostriatal neurons is the
hallmark of Parkinson disease (PD), and PET quantification of dopamine
transporters is a widely accepted method for differential diagnosis between
idiopathic PD and essential tremor. [18F]PR04.MZ is a new PET tracer with
excellent imaging properties allowing for precise quantification of striatal
and extrastriatal dopamine transporter. Here we describe our initial experience
with [18F]PR04.MZ PET/CT in a larger cohort of healthy controls
and PD patients as a proof-of-concept study for this tracer.
Methods: Eighteen healthy subjects, 19 early PD patients (Hoehn-Yahr I–II),
and 13 moderate-advanced PD patients (Hoehn-Yahr III–IV) underwent static
PET/CT scans 60 to 90 minutes after injection of 5.16 ± 1.03 mCi
(191 ± 38MBq) [18F]PR04.MZ. Specific binding ratios (SBRs)were calculated
for caudate nucleus, anterior putamen, posterior putamen, substantia nigra
(SNpc), compared between different groups and correlated with clinical ratings.
Results: [18F]PR04.MZ showed very high and specific uptake in the putamen,
caudate, and substantia nigra pars compacta and very low nonspecific
binding in other brain regions, and SBR values for the control group were
22.3 ± 4.1, 19.1 ± 3.5, and 5.4 ± 1.2, respectively.Areduction of SBR values
was observed in all regions and in both initial and moderate PD, ranging
from 35% to 89% (P < 0.001). The observed pattern of reduction was posterior
putamen > anterior putamen > substantia nigra pars compacta > caudate,
with contralateral posterior putamen being the most affected region.
Rostrocaudal depletion gradient was evident in all PD patients and progression
correlated with motor manifestations.
Conclusions: [18F]PR04.MZ PET/CT is a highly sensitive imaging modality
for the detection of dopaminergic deficit in nigrostriatal pathways in PD
Patrocinador
CORFO 13PIE-21682
Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT) FONDECYT 11130534
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Clinical Nuclear Medicine Volume 46, Number 2, February 2021
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