La maladie de Parkinson en France (serveur d'exploration)

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Relationships between striatal dopamine denervation and frontal executive tests in Parkinson's disease

Identifieur interne : 001306 ( PascalFrancis/Checkpoint ); précédent : 001305; suivant : 001307

Relationships between striatal dopamine denervation and frontal executive tests in Parkinson's disease

Auteurs : R. M. Marie [France] ; L. Barre [France] ; B. Dupuy [France] ; F. Viader [France] ; G. Defer [France] ; J. C. Baron [France]

Source :

RBID : Pascal:99-0126252

Descripteurs français

English descriptors

Abstract

Indirect evidence from human and monkey investigations supports the idea that impaired frontal tasks in Parkinson's disease (PD) may result from striato-frontal disruption caused by dopamine (DA) denervation of the caudate nucleus. To directly investigate this hypothesis, we used PET with 11C-S-Nomifensine (11C-S-NMF), a sensitive marker of striatal DA denervation, in 10 non-demented PD patients in whom two frontal executive tests, the object alternation (OA) and the conditional associative learning (CAL) tasks, thought to reflect mainly set-shifting/inhibition and planning, respectively, were given. In addition, the central executive function of verbal working memory was assessed with the Brown Peterson paradigm (BPP). We found a highly significant correlation between right caudate 11C-S-NMF specific binding and OA performance, less significant and reverse-direction correlations between CAL performance and putamen 11C-S-NMF binding, and no significant correlation with BPP performance. Thus, caudate DA denervation may subtend poor set-shifting/inhibition process in PD. Our results also point to distinct and complex relationships between striatal DA and specific frontal tasks. © 1999 Elsevier Science Ireland Ltd. All rights reserved.


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<div type="abstract" xml:lang="en">Indirect evidence from human and monkey investigations supports the idea that impaired frontal tasks in Parkinson's disease (PD) may result from striato-frontal disruption caused by dopamine (DA) denervation of the caudate nucleus. To directly investigate this hypothesis, we used PET with
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C-S-Nomifensine (
<sup>11</sup>
C-S-NMF), a sensitive marker of striatal DA denervation, in 10 non-demented PD patients in whom two frontal executive tests, the object alternation (OA) and the conditional associative learning (CAL) tasks, thought to reflect mainly set-shifting/inhibition and planning, respectively, were given. In addition, the central executive function of verbal working memory was assessed with the Brown Peterson paradigm (BPP). We found a highly significant correlation between right caudate
<sup>11</sup>
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<sup>11</sup>
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<sup>11</sup>
C-S-Nomifensine (
<sup>11</sup>
C-S-NMF), a sensitive marker of striatal DA denervation, in 10 non-demented PD patients in whom two frontal executive tests, the object alternation (OA) and the conditional associative learning (CAL) tasks, thought to reflect mainly set-shifting/inhibition and planning, respectively, were given. In addition, the central executive function of verbal working memory was assessed with the Brown Peterson paradigm (BPP). We found a highly significant correlation between right caudate
<sup>11</sup>
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<sup>11</sup>
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<s0>Neurotransmitter</s0>
<s5>23</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Neurotransmisor</s0>
<s5>23</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Catécholamine</s0>
<s5>24</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Catecholamine</s0>
<s5>24</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Catecolamina</s0>
<s5>24</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Système nerveux pathologie</s0>
<s5>38</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Nervous system diseases</s0>
<s5>38</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Sistema nervioso patología</s0>
<s5>38</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Système nerveux central pathologie</s0>
<s5>39</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Central nervous system disease</s0>
<s5>39</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Sistema nervosio central patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Encéphale pathologie</s0>
<s5>40</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Cerebral disorder</s0>
<s5>40</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Encéfalo patología</s0>
<s5>40</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE">
<s0>Extrapyramidal syndrome</s0>
<s5>41</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG">
<s0>Extrapyramidal syndrome</s0>
<s5>41</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA">
<s0>Extrapiramidal síndrome</s0>
<s5>41</s5>
</fC07>
<fC07 i1="10" i2="X" l="FRE">
<s0>Maladie dégénérative</s0>
<s5>42</s5>
</fC07>
<fC07 i1="10" i2="X" l="ENG">
<s0>Degenerative disease</s0>
<s5>42</s5>
</fC07>
<fC07 i1="10" i2="X" l="SPA">
<s0>Enfermedad degenerativa</s0>
<s5>42</s5>
</fC07>
<fN21>
<s1>074</s1>
</fN21>
</pA>
</standard>
</inist>
<affiliations>
<list>
<country>
<li>France</li>
</country>
<region>
<li>Basse-Normandie</li>
<li>Région Normandie</li>
</region>
<settlement>
<li>Caen</li>
</settlement>
</list>
<tree>
<country name="France">
<region name="Région Normandie">
<name sortKey="Marie, R M" sort="Marie, R M" uniqKey="Marie R" first="R. M." last="Marie">R. M. Marie</name>
</region>
<name sortKey="Baron, J C" sort="Baron, J C" uniqKey="Baron J" first="J. C." last="Baron">J. C. Baron</name>
<name sortKey="Barre, L" sort="Barre, L" uniqKey="Barre L" first="L." last="Barre">L. Barre</name>
<name sortKey="Defer, G" sort="Defer, G" uniqKey="Defer G" first="G." last="Defer">G. Defer</name>
<name sortKey="Dupuy, B" sort="Dupuy, B" uniqKey="Dupuy B" first="B." last="Dupuy">B. Dupuy</name>
<name sortKey="Marie, R M" sort="Marie, R M" uniqKey="Marie R" first="R. M." last="Marie">R. M. Marie</name>
<name sortKey="Viader, F" sort="Viader, F" uniqKey="Viader F" first="F." last="Viader">F. Viader</name>
</country>
</tree>
</affiliations>
</record>

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