[18F]FDOPA and [18F]CFT are both sensitive PET markers to detect presynaptic dopaminergic hypofunction in early Parkinson's disease
Identifieur interne : 001990 ( Main/Exploration ); précédent : 001989; suivant : 001991[18F]FDOPA and [18F]CFT are both sensitive PET markers to detect presynaptic dopaminergic hypofunction in early Parkinson's disease
Auteurs : Juha O. Rinne [Finlande] ; Elina Nurmi [Finlande] ; Hanna M. Ruottinen [Finlande] ; Jörgen Bergman [Finlande] ; Olli Eskola [Finlande] ; Olof Solin [Finlande]Source :
- Synapse [ 0887-4476 ] ; 2001-06-01.
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Abstract
The aim of this study was to compare two PET ligands, 6‐[18F]fluoro‐L‐dopa ([18F]FDOPA) and 18F‐labeled CFT, 2β‐carbomethoxy‐3β‐(4‐[18F]‐fluorophenyl)tropane ([18F]CFT), in detecting presynaptic dopaminergic hypofunction in early Parkinson's disease (PD). These ligands reflect different aspects of presynaptic dopaminergic function, since [18F]FDOPA mainly reflects 6‐[18F]fluorodopamine (fluorodopamine) synthesis and storage whereas [18F]CFT uptake is related to dopamine transporter function. Eight de novo patients with PD who had never been on antiparkinsonian medication were investigated with [18F]FDOPA and [18F]CFT PET. Five healthy volunteers were studied as controls. In PD patients, both [18F]FDOPA and [18F]CFT uptakes were significantly reduced both in the contralateral and ipsilateral anterior and posterior putamen. The reduction was greatest in the contralateral posterior putamen (to 28% of control mean for [18F]FDOPA, P < 0.0001 and to 16% for [18F]CFT, P < 0.0001). Individually, all patients' [18F]FDOPA and [18F]CFT uptake values in the contralateral anterior and posterior putamen were below 3 SD of the control mean. In the caudate nucleus, the mean uptake of both tracers was significantly reduced both ipsilaterally and contralaterally, but less severely than in the putamen (to 69% of the control mean for [18F]FDOPA, P = 0.003 and to 60% for [18F]CFT, P = 0.001 contralaterally). Our results show that both [18F]FDOPA as well as [18F]CFT sensitively detect presynaptic dopaminergic hypofunction in early PD. They demonstrate a considerable reduction of tracer uptake that is greatest in the posterior putamen, followed by the anterior putamen and the caudate nucleus. Synapse 40:193–200, 2001. © 2001 Wiley‐Liss, Inc.
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DOI: 10.1002/syn.1042
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<front><div type="abstract" xml:lang="en">The aim of this study was to compare two PET ligands, 6‐[18F]fluoro‐L‐dopa ([18F]FDOPA) and 18F‐labeled CFT, 2β‐carbomethoxy‐3β‐(4‐[18F]‐fluorophenyl)tropane ([18F]CFT), in detecting presynaptic dopaminergic hypofunction in early Parkinson's disease (PD). These ligands reflect different aspects of presynaptic dopaminergic function, since [18F]FDOPA mainly reflects 6‐[18F]fluorodopamine (fluorodopamine) synthesis and storage whereas [18F]CFT uptake is related to dopamine transporter function. Eight de novo patients with PD who had never been on antiparkinsonian medication were investigated with [18F]FDOPA and [18F]CFT PET. Five healthy volunteers were studied as controls. In PD patients, both [18F]FDOPA and [18F]CFT uptakes were significantly reduced both in the contralateral and ipsilateral anterior and posterior putamen. The reduction was greatest in the contralateral posterior putamen (to 28% of control mean for [18F]FDOPA, P < 0.0001 and to 16% for [18F]CFT, P < 0.0001). Individually, all patients' [18F]FDOPA and [18F]CFT uptake values in the contralateral anterior and posterior putamen were below 3 SD of the control mean. In the caudate nucleus, the mean uptake of both tracers was significantly reduced both ipsilaterally and contralaterally, but less severely than in the putamen (to 69% of the control mean for [18F]FDOPA, P = 0.003 and to 60% for [18F]CFT, P = 0.001 contralaterally). Our results show that both [18F]FDOPA as well as [18F]CFT sensitively detect presynaptic dopaminergic hypofunction in early PD. They demonstrate a considerable reduction of tracer uptake that is greatest in the posterior putamen, followed by the anterior putamen and the caudate nucleus. Synapse 40:193–200, 2001. © 2001 Wiley‐Liss, Inc.</div>
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