[123I]beta-CIT single-photon emission tomography in DOPA-responsive dystonia.
Identifieur interne : 004D22 ( Ncbi/Merge ); précédent : 004D21; suivant : 004D23[123I]beta-CIT single-photon emission tomography in DOPA-responsive dystonia.
Auteurs : M. Naumann [Allemagne] ; W. Pirker ; K. Reiners ; K. Lange ; G. Becker ; T. BrückeSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 1997.
English descriptors
- KwdEn :
- Adult, Aged, Binding Sites, Cerebellum (metabolism), Cerebellum (radionuclide imaging), Corpus Striatum (metabolism), Corpus Striatum (radionuclide imaging), Diagnosis, Differential, Dopamine (metabolism), Dystonia (drug therapy), Dystonia (radionuclide imaging), Female, Humans, Levodopa (therapeutic use), Middle Aged, Radioactive Tracers, Tomography, Emission-Computed, Single-Photon.
- MESH :
- chemical , metabolism : Dopamine.
- drug therapy : Dystonia.
- metabolism : Cerebellum, Corpus Striatum.
- radionuclide imaging : Cerebellum, Corpus Striatum, Dystonia.
- chemical , therapeutic use : Levodopa.
- Adult, Aged, Binding Sites, Diagnosis, Differential, Female, Humans, Middle Aged, Radioactive Tracers, Tomography, Emission-Computed, Single-Photon.
Abstract
The radiotracer [123I]beta-CIT is a sensitive marker of dopamine uptake sites that can be used to visualize dopaminergic nerve endings in vivo in the human brain. We report on [123I]beta-CIT single-photon emission computed tomography (SPECT) findings in a patient with DOPA-responsive dystonia (DRD). [123I]beta-CIT SPECT showed a striatal radiotracer uptake in the upper range of normal, indicating intact dopamine transporters and structural integrity of nigrostriatal neurons. This differentiates DRD from clinically similar cases with juvenile-onset parkinsonism with dystonia that have a considerable poorer prognosis. [123I]-beta-CIT SPECT may provide a method equally as useful as fluorodopa positron emission tomography in DRD.
DOI: 10.1002/mds.870120330
PubMed: 9159746
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pubmed:9159746Le document en format XML
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<author><name sortKey="Naumann, M" sort="Naumann, M" uniqKey="Naumann M" first="M" last="Naumann">M. Naumann</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Neurology, Universities of Würzburg, Germany.</nlm:affiliation>
<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Neurology, Universities of Würzburg</wicri:regionArea>
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<wicri:noRegion>Universities of Würzburg</wicri:noRegion>
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<author><name sortKey="Pirker, W" sort="Pirker, W" uniqKey="Pirker W" first="W" last="Pirker">W. Pirker</name>
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<author><name sortKey="Reiners, K" sort="Reiners, K" uniqKey="Reiners K" first="K" last="Reiners">K. Reiners</name>
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<author><name sortKey="Lange, K" sort="Lange, K" uniqKey="Lange K" first="K" last="Lange">K. Lange</name>
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<author><name sortKey="Becker, G" sort="Becker, G" uniqKey="Becker G" first="G" last="Becker">G. Becker</name>
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<author><name sortKey="Brucke, T" sort="Brucke, T" uniqKey="Brucke T" first="T" last="Brücke">T. Brücke</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">[123I]beta-CIT single-photon emission tomography in DOPA-responsive dystonia.</title>
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<term>Aged</term>
<term>Binding Sites</term>
<term>Cerebellum (metabolism)</term>
<term>Cerebellum (radionuclide imaging)</term>
<term>Corpus Striatum (metabolism)</term>
<term>Corpus Striatum (radionuclide imaging)</term>
<term>Diagnosis, Differential</term>
<term>Dopamine (metabolism)</term>
<term>Dystonia (drug therapy)</term>
<term>Dystonia (radionuclide imaging)</term>
<term>Female</term>
<term>Humans</term>
<term>Levodopa (therapeutic use)</term>
<term>Middle Aged</term>
<term>Radioactive Tracers</term>
<term>Tomography, Emission-Computed, Single-Photon</term>
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<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Dopamine</term>
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</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Cerebellum</term>
<term>Corpus Striatum</term>
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<term>Aged</term>
<term>Binding Sites</term>
<term>Diagnosis, Differential</term>
<term>Female</term>
<term>Humans</term>
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<front><div type="abstract" xml:lang="en">The radiotracer [123I]beta-CIT is a sensitive marker of dopamine uptake sites that can be used to visualize dopaminergic nerve endings in vivo in the human brain. We report on [123I]beta-CIT single-photon emission computed tomography (SPECT) findings in a patient with DOPA-responsive dystonia (DRD). [123I]beta-CIT SPECT showed a striatal radiotracer uptake in the upper range of normal, indicating intact dopamine transporters and structural integrity of nigrostriatal neurons. This differentiates DRD from clinically similar cases with juvenile-onset parkinsonism with dystonia that have a considerable poorer prognosis. [123I]-beta-CIT SPECT may provide a method equally as useful as fluorodopa positron emission tomography in DRD.</div>
</front>
</TEI>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
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<ArticleTitle>[123I]beta-CIT single-photon emission tomography in DOPA-responsive dystonia.</ArticleTitle>
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<Abstract><AbstractText>The radiotracer [123I]beta-CIT is a sensitive marker of dopamine uptake sites that can be used to visualize dopaminergic nerve endings in vivo in the human brain. We report on [123I]beta-CIT single-photon emission computed tomography (SPECT) findings in a patient with DOPA-responsive dystonia (DRD). [123I]beta-CIT SPECT showed a striatal radiotracer uptake in the upper range of normal, indicating intact dopamine transporters and structural integrity of nigrostriatal neurons. This differentiates DRD from clinically similar cases with juvenile-onset parkinsonism with dystonia that have a considerable poorer prognosis. [123I]-beta-CIT SPECT may provide a method equally as useful as fluorodopa positron emission tomography in DRD.</AbstractText>
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