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Non-motor dopamine withdrawal syndrome after surgery for Parkinsons disease: predictors and underlying mesolimbic denervation

Identifieur interne : 000470 ( Main/Corpus ); précédent : 000469; suivant : 000471

Non-motor dopamine withdrawal syndrome after surgery for Parkinsons disease: predictors and underlying mesolimbic denervation

Auteurs : Stphane Thobois ; Claire Ardouin ; Eugnie Lhomme ; Hlne Klinger ; Christelle Lagrange ; Jing Xie ; Valrie Fraix ; Maria Clara Coelho Braga ; Rachid Hassani ; Andrea Kistner ; Alexandra Juphard ; Eric Seigneuret ; Stephan Chabardes ; Patrick Mertens ; Gustavo Polo ; Anthonin Reilhac ; Nicolas Costes ; Didier Lebars ; Marc Savasta ; Lon Tremblay ; Jean-Louis Quesada ; Jean-Luc Bosson ; Alim-Louis Benabid ; Emmanuel Broussolle ; Pierre Pollak ; Paul Krack

Source :

RBID : ISTEX:EAB99310FD3EC51E1AE0E5946614A8EF666A6094

Abstract

Apathy has been reported to occur after subthalamic nucleus stimulation, a treatment of motor complications in advanced Parkinsons disease. We carried out a prospective study of the occurrence of apathy and associated symptoms, predictors and mechanisms in the year following subthalamic stimulation. Dopamine agonist drugs were discontinued immediately after surgery and levodopa was markedly reduced within 2 weeks. Apathy and depression were assessed monthly, using the Starkstein apathy scale and the Beck Depression Inventory. Dopamine agonists were re-introduced if patients developed apathy or depression. Preoperative non-motor fluctuations were evaluated using the Ardouin Scale. Depression, apathy and anxiety were evaluated both on and off levodopa. Analysis of predictors of apathy was performed using a Cox proportional hazard model. Twelve patients who developed apathy and a control group of 13 patients who did not underwent [11C]-raclopride positron emission tomography scanning before and after oral intake of methylphenidate. In 63 patients with Parkinsons disease treated with subthalamic stimulation, dopaminergic treatment was decreased by 82 after surgery. Apathy occurred after a mean of 4.7 (3.38.2) months in 34 patients and was reversible in half of these by the 12-month follow-up. Seventeen patients developed transient depression after 5.7 (4.79.3) months and these fell into the apathy group with one single exception. At baseline, fluctuations in depression, apathy and anxiety scores were greater in the group with apathy. Fluctuations in apathy, depression and anxiety ratings during a baseline levodopa challenge were also significant predictors of postoperative apathy in univariate analysis, but not motor and cognitive states or the level of reduction of dopaminergic medication. The multivariate model identified non-motor fluctuations in everyday life and anxiety score during the baseline levodopa challenge as two independent significant predictors of postoperative apathy. Without methylphenidate, [11C]-raclopride binding potential values were greater in apathetic patients bilaterally in the orbitofrontal, dorsolateral prefrontal, posterior cingulate and temporal cortices, left striatum and right amygdala, reflecting greater dopamine D2/D3 receptor density and/or reduced synaptic dopamine level in these areas. The variations of [11C]-raclopride binding potential values induced by methylphenidate were greater in non-apathetic patients in the left orbitofrontal cortex, dorsolateral prefrontal cortex, thalamus and internal globus pallidus and bilaterally in the anterior and posterior cingulate cortices, consistent with a more important capacity to release dopamine. Non-motor fluctuations are related to mesolimbic dopaminergic denervation. Apathy, depression and anxiety can occur after surgery as a delayed dopamine withdrawal syndrome. A varying extent of mesolimbic dopaminergic denervation and differences in dopaminergic treatment largely determine mood, anxiety and motivation in patients with Parkinsons disease, contributing to different non-motor phenotypes.

Url:
DOI: 10.1093/brain/awq032

Links to Exploration step

ISTEX:EAB99310FD3EC51E1AE0E5946614A8EF666A6094

Le document en format XML

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<name sortKey="Klinger, Hlne" sort="Klinger, Hlne" uniqKey="Klinger H" first="Hlne" last="Klinger">Hlne Klinger</name>
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<name sortKey="Coelho Braga, Maria Clara" sort="Coelho Braga, Maria Clara" uniqKey="Coelho Braga M" first="Maria Clara" last="Coelho Braga">Maria Clara Coelho Braga</name>
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<name sortKey="Hassani, Rachid" sort="Hassani, Rachid" uniqKey="Hassani R" first="Rachid" last="Hassani">Rachid Hassani</name>
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<mods:affiliation>5 Hpital des Spcialits, Service de Neurologie A, Rabat, Morocco</mods:affiliation>
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<mods:affiliation>6 Neurosurgery Department, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
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<name sortKey="Chabardes, Stephan" sort="Chabardes, Stephan" uniqKey="Chabardes S" first="Stephan" last="Chabardes">Stephan Chabardes</name>
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<name sortKey="Mertens, Patrick" sort="Mertens, Patrick" uniqKey="Mertens P" first="Patrick" last="Mertens">Patrick Mertens</name>
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<mods:affiliation>7 Universit Lyon I; Hospices Civils de Lyon, Hpital Neurologique Pierre Wertheimer, Service de Neurochirurgie A, 69003 Lyon, France</mods:affiliation>
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<name sortKey="Polo, Gustavo" sort="Polo, Gustavo" uniqKey="Polo G" first="Gustavo" last="Polo">Gustavo Polo</name>
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<name sortKey="Costes, Nicolas" sort="Costes, Nicolas" uniqKey="Costes N" first="Nicolas" last="Costes">Nicolas Costes</name>
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<name sortKey="Lebars, Didier" sort="Lebars, Didier" uniqKey="Lebars D" first="Didier" last="Lebars">Didier Lebars</name>
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<name sortKey="Savasta, Marc" sort="Savasta, Marc" uniqKey="Savasta M" first="Marc" last="Savasta">Marc Savasta</name>
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<name sortKey="Tremblay, Lon" sort="Tremblay, Lon" uniqKey="Tremblay L" first="Lon" last="Tremblay">Lon Tremblay</name>
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<mods:affiliation>2 CNRS, UMR 5229, Centre de Neurosciences Cognitives, 69003 Lyon, France</mods:affiliation>
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<name sortKey="Quesada, Jean Louis" sort="Quesada, Jean Louis" uniqKey="Quesada J" first="Jean-Louis" last="Quesada">Jean-Louis Quesada</name>
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<mods:affiliation>9 Centre dInvestigation Clinique, CHU Grenoble, Universit Joseph Fourier, 38043 Grenoble, France</mods:affiliation>
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<name sortKey="Bosson, Jean Luc" sort="Bosson, Jean Luc" uniqKey="Bosson J" first="Jean-Luc" last="Bosson">Jean-Luc Bosson</name>
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<mods:affiliation>9 Centre dInvestigation Clinique, CHU Grenoble, Universit Joseph Fourier, 38043 Grenoble, France</mods:affiliation>
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<name sortKey="Benabid, Alim Louis" sort="Benabid, Alim Louis" uniqKey="Benabid A" first="Alim-Louis" last="Benabid">Alim-Louis Benabid</name>
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<mods:affiliation>6 Neurosurgery Department, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
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<mods:affiliation>10 Clinatec, DRT/LETI, CEA-Grenoble, 38000 Grenoble, France</mods:affiliation>
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<name sortKey="Broussolle, Emmanuel" sort="Broussolle, Emmanuel" uniqKey="Broussolle E" first="Emmanuel" last="Broussolle">Emmanuel Broussolle</name>
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<name sortKey="Pollak, Pierre" sort="Pollak, Pierre" uniqKey="Pollak P" first="Pierre" last="Pollak">Pierre Pollak</name>
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<mods:affiliation>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
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<name sortKey="Krack, Paul" sort="Krack, Paul" uniqKey="Krack P" first="Paul" last="Krack">Paul Krack</name>
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<mods:affiliation>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
</affiliation>
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<mods:affiliation>4 INSERM, Unit 836, Grenoble Institut des Neurosciences, 38043 Grenoble, France</mods:affiliation>
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<mods:affiliation>E-mail: paul.krack@ujf-grenoble.fr</mods:affiliation>
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<title level="a">Non-motor dopamine withdrawal syndrome after surgery for Parkinsons disease: predictors and underlying mesolimbic denervation</title>
<author>
<name sortKey="Thobois, Stphane" sort="Thobois, Stphane" uniqKey="Thobois S" first="Stphane" last="Thobois">Stphane Thobois</name>
<affiliation>
<mods:affiliation>1 Universit Lyon I, Hospices Civils de Lyon, Hpital Neurologique Pierre Wertheimer, Service de Neurologie C, 69003 Lyon, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>2 CNRS, UMR 5229, Centre de Neurosciences Cognitives, 69003 Lyon, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Ardouin, Claire" sort="Ardouin, Claire" uniqKey="Ardouin C" first="Claire" last="Ardouin">Claire Ardouin</name>
<affiliation>
<mods:affiliation>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>4 INSERM, Unit 836, Grenoble Institut des Neurosciences, 38043 Grenoble, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Lhomme, Eugnie" sort="Lhomme, Eugnie" uniqKey="Lhomme E" first="Eugnie" last="Lhomme">Eugnie Lhomme</name>
<affiliation>
<mods:affiliation>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>4 INSERM, Unit 836, Grenoble Institut des Neurosciences, 38043 Grenoble, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Klinger, Hlne" sort="Klinger, Hlne" uniqKey="Klinger H" first="Hlne" last="Klinger">Hlne Klinger</name>
<affiliation>
<mods:affiliation>1 Universit Lyon I, Hospices Civils de Lyon, Hpital Neurologique Pierre Wertheimer, Service de Neurologie C, 69003 Lyon, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>2 CNRS, UMR 5229, Centre de Neurosciences Cognitives, 69003 Lyon, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Lagrange, Christelle" sort="Lagrange, Christelle" uniqKey="Lagrange C" first="Christelle" last="Lagrange">Christelle Lagrange</name>
<affiliation>
<mods:affiliation>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>4 INSERM, Unit 836, Grenoble Institut des Neurosciences, 38043 Grenoble, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Xie, Jing" sort="Xie, Jing" uniqKey="Xie J" first="Jing" last="Xie">Jing Xie</name>
<affiliation>
<mods:affiliation>1 Universit Lyon I, Hospices Civils de Lyon, Hpital Neurologique Pierre Wertheimer, Service de Neurologie C, 69003 Lyon, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>2 CNRS, UMR 5229, Centre de Neurosciences Cognitives, 69003 Lyon, France</mods:affiliation>
</affiliation>
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<author>
<name sortKey="Fraix, Valrie" sort="Fraix, Valrie" uniqKey="Fraix V" first="Valrie" last="Fraix">Valrie Fraix</name>
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<mods:affiliation>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>4 INSERM, Unit 836, Grenoble Institut des Neurosciences, 38043 Grenoble, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Coelho Braga, Maria Clara" sort="Coelho Braga, Maria Clara" uniqKey="Coelho Braga M" first="Maria Clara" last="Coelho Braga">Maria Clara Coelho Braga</name>
<affiliation>
<mods:affiliation>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Hassani, Rachid" sort="Hassani, Rachid" uniqKey="Hassani R" first="Rachid" last="Hassani">Rachid Hassani</name>
<affiliation>
<mods:affiliation>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>5 Hpital des Spcialits, Service de Neurologie A, Rabat, Morocco</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Kistner, Andrea" sort="Kistner, Andrea" uniqKey="Kistner A" first="Andrea" last="Kistner">Andrea Kistner</name>
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<mods:affiliation>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>4 INSERM, Unit 836, Grenoble Institut des Neurosciences, 38043 Grenoble, France</mods:affiliation>
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<name sortKey="Juphard, Alexandra" sort="Juphard, Alexandra" uniqKey="Juphard A" first="Alexandra" last="Juphard">Alexandra Juphard</name>
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<mods:affiliation>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Seigneuret, Eric" sort="Seigneuret, Eric" uniqKey="Seigneuret E" first="Eric" last="Seigneuret">Eric Seigneuret</name>
<affiliation>
<mods:affiliation>4 INSERM, Unit 836, Grenoble Institut des Neurosciences, 38043 Grenoble, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>6 Neurosurgery Department, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Chabardes, Stephan" sort="Chabardes, Stephan" uniqKey="Chabardes S" first="Stephan" last="Chabardes">Stephan Chabardes</name>
<affiliation>
<mods:affiliation>4 INSERM, Unit 836, Grenoble Institut des Neurosciences, 38043 Grenoble, France</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>6 Neurosurgery Department, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Mertens, Patrick" sort="Mertens, Patrick" uniqKey="Mertens P" first="Patrick" last="Mertens">Patrick Mertens</name>
<affiliation>
<mods:affiliation>7 Universit Lyon I; Hospices Civils de Lyon, Hpital Neurologique Pierre Wertheimer, Service de Neurochirurgie A, 69003 Lyon, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Polo, Gustavo" sort="Polo, Gustavo" uniqKey="Polo G" first="Gustavo" last="Polo">Gustavo Polo</name>
<affiliation>
<mods:affiliation>7 Universit Lyon I; Hospices Civils de Lyon, Hpital Neurologique Pierre Wertheimer, Service de Neurochirurgie A, 69003 Lyon, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Reilhac, Anthonin" sort="Reilhac, Anthonin" uniqKey="Reilhac A" first="Anthonin" last="Reilhac">Anthonin Reilhac</name>
<affiliation>
<mods:affiliation>8 CERMEPImagerie du vivant, 69677 Bron, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Costes, Nicolas" sort="Costes, Nicolas" uniqKey="Costes N" first="Nicolas" last="Costes">Nicolas Costes</name>
<affiliation>
<mods:affiliation>8 CERMEPImagerie du vivant, 69677 Bron, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Lebars, Didier" sort="Lebars, Didier" uniqKey="Lebars D" first="Didier" last="Lebars">Didier Lebars</name>
<affiliation>
<mods:affiliation>8 CERMEPImagerie du vivant, 69677 Bron, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Savasta, Marc" sort="Savasta, Marc" uniqKey="Savasta M" first="Marc" last="Savasta">Marc Savasta</name>
<affiliation>
<mods:affiliation>4 INSERM, Unit 836, Grenoble Institut des Neurosciences, 38043 Grenoble, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Tremblay, Lon" sort="Tremblay, Lon" uniqKey="Tremblay L" first="Lon" last="Tremblay">Lon Tremblay</name>
<affiliation>
<mods:affiliation>2 CNRS, UMR 5229, Centre de Neurosciences Cognitives, 69003 Lyon, France</mods:affiliation>
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<div type="abstract">Apathy has been reported to occur after subthalamic nucleus stimulation, a treatment of motor complications in advanced Parkinsons disease. We carried out a prospective study of the occurrence of apathy and associated symptoms, predictors and mechanisms in the year following subthalamic stimulation. Dopamine agonist drugs were discontinued immediately after surgery and levodopa was markedly reduced within 2 weeks. Apathy and depression were assessed monthly, using the Starkstein apathy scale and the Beck Depression Inventory. Dopamine agonists were re-introduced if patients developed apathy or depression. Preoperative non-motor fluctuations were evaluated using the Ardouin Scale. Depression, apathy and anxiety were evaluated both on and off levodopa. Analysis of predictors of apathy was performed using a Cox proportional hazard model. Twelve patients who developed apathy and a control group of 13 patients who did not underwent [11C]-raclopride positron emission tomography scanning before and after oral intake of methylphenidate. In 63 patients with Parkinsons disease treated with subthalamic stimulation, dopaminergic treatment was decreased by 82 after surgery. Apathy occurred after a mean of 4.7 (3.38.2) months in 34 patients and was reversible in half of these by the 12-month follow-up. Seventeen patients developed transient depression after 5.7 (4.79.3) months and these fell into the apathy group with one single exception. At baseline, fluctuations in depression, apathy and anxiety scores were greater in the group with apathy. Fluctuations in apathy, depression and anxiety ratings during a baseline levodopa challenge were also significant predictors of postoperative apathy in univariate analysis, but not motor and cognitive states or the level of reduction of dopaminergic medication. The multivariate model identified non-motor fluctuations in everyday life and anxiety score during the baseline levodopa challenge as two independent significant predictors of postoperative apathy. Without methylphenidate, [11C]-raclopride binding potential values were greater in apathetic patients bilaterally in the orbitofrontal, dorsolateral prefrontal, posterior cingulate and temporal cortices, left striatum and right amygdala, reflecting greater dopamine D2/D3 receptor density and/or reduced synaptic dopamine level in these areas. The variations of [11C]-raclopride binding potential values induced by methylphenidate were greater in non-apathetic patients in the left orbitofrontal cortex, dorsolateral prefrontal cortex, thalamus and internal globus pallidus and bilaterally in the anterior and posterior cingulate cortices, consistent with a more important capacity to release dopamine. Non-motor fluctuations are related to mesolimbic dopaminergic denervation. Apathy, depression and anxiety can occur after surgery as a delayed dopamine withdrawal syndrome. A varying extent of mesolimbic dopaminergic denervation and differences in dopaminergic treatment largely determine mood, anxiety and motivation in patients with Parkinsons disease, contributing to different non-motor phenotypes.</div>
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<abstract>Apathy has been reported to occur after subthalamic nucleus stimulation, a treatment of motor complications in advanced Parkinsons disease. We carried out a prospective study of the occurrence of apathy and associated symptoms, predictors and mechanisms in the year following subthalamic stimulation. Dopamine agonist drugs were discontinued immediately after surgery and levodopa was markedly reduced within 2 weeks. Apathy and depression were assessed monthly, using the Starkstein apathy scale and the Beck Depression Inventory. Dopamine agonists were re-introduced if patients developed apathy or depression. Preoperative non-motor fluctuations were evaluated using the Ardouin Scale. Depression, apathy and anxiety were evaluated both on and off levodopa. Analysis of predictors of apathy was performed using a Cox proportional hazard model. Twelve patients who developed apathy and a control group of 13 patients who did not underwent [11C]-raclopride positron emission tomography scanning before and after oral intake of methylphenidate. In 63 patients with Parkinsons disease treated with subthalamic stimulation, dopaminergic treatment was decreased by 82 after surgery. Apathy occurred after a mean of 4.7 (3.38.2) months in 34 patients and was reversible in half of these by the 12-month follow-up. Seventeen patients developed transient depression after 5.7 (4.79.3) months and these fell into the apathy group with one single exception. At baseline, fluctuations in depression, apathy and anxiety scores were greater in the group with apathy. Fluctuations in apathy, depression and anxiety ratings during a baseline levodopa challenge were also significant predictors of postoperative apathy in univariate analysis, but not motor and cognitive states or the level of reduction of dopaminergic medication. The multivariate model identified non-motor fluctuations in everyday life and anxiety score during the baseline levodopa challenge as two independent significant predictors of postoperative apathy. Without methylphenidate, [11C]-raclopride binding potential values were greater in apathetic patients bilaterally in the orbitofrontal, dorsolateral prefrontal, posterior cingulate and temporal cortices, left striatum and right amygdala, reflecting greater dopamine D2/D3 receptor density and/or reduced synaptic dopamine level in these areas. The variations of [11C]-raclopride binding potential values induced by methylphenidate were greater in non-apathetic patients in the left orbitofrontal cortex, dorsolateral prefrontal cortex, thalamus and internal globus pallidus and bilaterally in the anterior and posterior cingulate cortices, consistent with a more important capacity to release dopamine. Non-motor fluctuations are related to mesolimbic dopaminergic denervation. Apathy, depression and anxiety can occur after surgery as a delayed dopamine withdrawal syndrome. A varying extent of mesolimbic dopaminergic denervation and differences in dopaminergic treatment largely determine mood, anxiety and motivation in patients with Parkinsons disease, contributing to different non-motor phenotypes.</abstract>
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<affiliation>4 INSERM, Unit 836, Grenoble Institut des Neurosciences, 38043 Grenoble, France</affiliation>
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<author>
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<forename type="first">Patrick</forename>
<surname>Mertens</surname>
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<author>
<persName>
<forename type="first">Gustavo</forename>
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<author>
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<forename type="first">Anthonin</forename>
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</author>
<author>
<persName>
<forename type="first">Nicolas</forename>
<surname>Costes</surname>
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<affiliation>8 CERMEPImagerie du vivant, 69677 Bron, France</affiliation>
</author>
<author>
<persName>
<forename type="first">Didier</forename>
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<author>
<persName>
<forename type="first">Marc</forename>
<surname>Savasta</surname>
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<author>
<persName>
<forename type="first">Lon</forename>
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<affiliation>2 CNRS, UMR 5229, Centre de Neurosciences Cognitives, 69003 Lyon, France</affiliation>
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<author>
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<forename type="first">Jean-Louis</forename>
<surname>Quesada</surname>
</persName>
<affiliation>9 Centre dInvestigation Clinique, CHU Grenoble, Universit Joseph Fourier, 38043 Grenoble, France</affiliation>
</author>
<author>
<persName>
<forename type="first">Jean-Luc</forename>
<surname>Bosson</surname>
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<affiliation>9 Centre dInvestigation Clinique, CHU Grenoble, Universit Joseph Fourier, 38043 Grenoble, France</affiliation>
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<author>
<persName>
<forename type="first">Alim-Louis</forename>
<surname>Benabid</surname>
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<affiliation>10 Clinatec, DRT/LETI, CEA-Grenoble, 38000 Grenoble, France</affiliation>
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<author>
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<forename type="first">Emmanuel</forename>
<surname>Broussolle</surname>
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<affiliation>1 Universit Lyon I, Hospices Civils de Lyon, Hpital Neurologique Pierre Wertheimer, Service de Neurologie C, 69003 Lyon, France</affiliation>
<affiliation>2 CNRS, UMR 5229, Centre de Neurosciences Cognitives, 69003 Lyon, France</affiliation>
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<author>
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<forename type="first">Pierre</forename>
<surname>Pollak</surname>
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<affiliation>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</affiliation>
<affiliation>4 INSERM, Unit 836, Grenoble Institut des Neurosciences, 38043 Grenoble, France</affiliation>
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<p>Apathy has been reported to occur after subthalamic nucleus stimulation, a treatment of motor complications in advanced Parkinsons disease. We carried out a prospective study of the occurrence of apathy and associated symptoms, predictors and mechanisms in the year following subthalamic stimulation. Dopamine agonist drugs were discontinued immediately after surgery and levodopa was markedly reduced within 2 weeks. Apathy and depression were assessed monthly, using the Starkstein apathy scale and the Beck Depression Inventory. Dopamine agonists were re-introduced if patients developed apathy or depression. Preoperative non-motor fluctuations were evaluated using the Ardouin Scale. Depression, apathy and anxiety were evaluated both on and off levodopa. Analysis of predictors of apathy was performed using a Cox proportional hazard model. Twelve patients who developed apathy and a control group of 13 patients who did not underwent [11C]-raclopride positron emission tomography scanning before and after oral intake of methylphenidate. In 63 patients with Parkinsons disease treated with subthalamic stimulation, dopaminergic treatment was decreased by 82 after surgery. Apathy occurred after a mean of 4.7 (3.38.2) months in 34 patients and was reversible in half of these by the 12-month follow-up. Seventeen patients developed transient depression after 5.7 (4.79.3) months and these fell into the apathy group with one single exception. At baseline, fluctuations in depression, apathy and anxiety scores were greater in the group with apathy. Fluctuations in apathy, depression and anxiety ratings during a baseline levodopa challenge were also significant predictors of postoperative apathy in univariate analysis, but not motor and cognitive states or the level of reduction of dopaminergic medication. The multivariate model identified non-motor fluctuations in everyday life and anxiety score during the baseline levodopa challenge as two independent significant predictors of postoperative apathy. Without methylphenidate, [11C]-raclopride binding potential values were greater in apathetic patients bilaterally in the orbitofrontal, dorsolateral prefrontal, posterior cingulate and temporal cortices, left striatum and right amygdala, reflecting greater dopamine D2/D3 receptor density and/or reduced synaptic dopamine level in these areas. The variations of [11C]-raclopride binding potential values induced by methylphenidate were greater in non-apathetic patients in the left orbitofrontal cortex, dorsolateral prefrontal cortex, thalamus and internal globus pallidus and bilaterally in the anterior and posterior cingulate cortices, consistent with a more important capacity to release dopamine. Non-motor fluctuations are related to mesolimbic dopaminergic denervation. Apathy, depression and anxiety can occur after surgery as a delayed dopamine withdrawal syndrome. A varying extent of mesolimbic dopaminergic denervation and differences in dopaminergic treatment largely determine mood, anxiety and motivation in patients with Parkinsons disease, contributing to different non-motor phenotypes.</p>
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<name>
<surname>Thobois</surname>
<given-names>Stéphane</given-names>
</name>
<xref ref-type="aff" rid="AFF1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="AFF2">
<sup>2</sup>
</xref>
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<name>
<surname>Ardouin</surname>
<given-names>Claire</given-names>
</name>
<xref ref-type="aff" rid="AFF3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="AFF4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Lhommée</surname>
<given-names>Eugénie</given-names>
</name>
<xref ref-type="aff" rid="AFF3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="AFF4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Klinger</surname>
<given-names>Hélène</given-names>
</name>
<xref ref-type="aff" rid="AFF1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="AFF2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Lagrange</surname>
<given-names>Christelle</given-names>
</name>
<xref ref-type="aff" rid="AFF3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="AFF4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Xie</surname>
<given-names>Jing</given-names>
</name>
<xref ref-type="aff" rid="AFF1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="AFF2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Fraix</surname>
<given-names>Valérie</given-names>
</name>
<xref ref-type="aff" rid="AFF3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="AFF4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Coelho Braga</surname>
<given-names>Maria Clara</given-names>
</name>
<xref ref-type="aff" rid="AFF3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Hassani</surname>
<given-names>Rachid</given-names>
</name>
<xref ref-type="aff" rid="AFF3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="AFF5">
<sup>5</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kistner</surname>
<given-names>Andrea</given-names>
</name>
<xref ref-type="aff" rid="AFF3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="AFF4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Juphard</surname>
<given-names>Alexandra</given-names>
</name>
<xref ref-type="aff" rid="AFF3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Seigneuret</surname>
<given-names>Eric</given-names>
</name>
<xref ref-type="aff" rid="AFF4">
<sup>4</sup>
</xref>
<xref ref-type="aff" rid="AFF6">
<sup>6</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Chabardes</surname>
<given-names>Stephan</given-names>
</name>
<xref ref-type="aff" rid="AFF4">
<sup>4</sup>
</xref>
<xref ref-type="aff" rid="AFF6">
<sup>6</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mertens</surname>
<given-names>Patrick</given-names>
</name>
<xref ref-type="aff" rid="AFF7">
<sup>7</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Polo</surname>
<given-names>Gustavo</given-names>
</name>
<xref ref-type="aff" rid="AFF7">
<sup>7</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Reilhac</surname>
<given-names>Anthonin</given-names>
</name>
<xref ref-type="aff" rid="AFF8">
<sup>8</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Costes</surname>
<given-names>Nicolas</given-names>
</name>
<xref ref-type="aff" rid="AFF8">
<sup>8</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>LeBars</surname>
<given-names>Didier</given-names>
</name>
<xref ref-type="aff" rid="AFF8">
<sup>8</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Savasta</surname>
<given-names>Marc</given-names>
</name>
<xref ref-type="aff" rid="AFF4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tremblay</surname>
<given-names>Léon</given-names>
</name>
<xref ref-type="aff" rid="AFF2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Quesada</surname>
<given-names>Jean-Louis</given-names>
</name>
<xref ref-type="aff" rid="AFF9">
<sup>9</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Bosson</surname>
<given-names>Jean-Luc</given-names>
</name>
<xref ref-type="aff" rid="AFF9">
<sup>9</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Benabid</surname>
<given-names>Alim-Louis</given-names>
</name>
<xref ref-type="aff" rid="AFF6">
<sup>6</sup>
</xref>
<xref ref-type="aff" rid="AFF10">
<sup>10</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Broussolle</surname>
<given-names>Emmanuel</given-names>
</name>
<xref ref-type="aff" rid="AFF1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="AFF2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Pollak</surname>
<given-names>Pierre</given-names>
</name>
<xref ref-type="aff" rid="AFF3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="AFF4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Krack</surname>
<given-names>Paul</given-names>
</name>
<xref ref-type="aff" rid="AFF3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="AFF4">
<sup>4</sup>
</xref>
</contrib>
</contrib-group>
<aff id="AFF1">1 Université Lyon I, Hospices Civils de Lyon, Hôpital Neurologique Pierre Wertheimer, Service de Neurologie C, 69003 Lyon, France</aff>
<aff id="AFF2">2 CNRS, UMR 5229, Centre de Neurosciences Cognitives, 69003 Lyon, France</aff>
<aff id="AFF3">3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</aff>
<aff id="AFF4">4 INSERM, Unité 836, Grenoble Institut des Neurosciences, 38043 Grenoble, France</aff>
<aff id="AFF5">5 Hôpital des Spécialités, Service de Neurologie A, Rabat, Morocco</aff>
<aff id="AFF6">6 Neurosurgery Department, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</aff>
<aff id="AFF7">7 Université Lyon I; Hospices Civils de Lyon, Hôpital Neurologique Pierre Wertheimer, Service de Neurochirurgie A, 69003 Lyon, France</aff>
<aff id="AFF8">8 CERMEP—Imagerie du vivant, 69677 Bron, France</aff>
<aff id="AFF9">9 Centre d’Investigation Clinique, CHU Grenoble, Université Joseph Fourier, 38043 Grenoble, France</aff>
<aff id="AFF10">10 Clinatec, DRT/LETI, CEA-Grenoble, 38000 Grenoble, France</aff>
<author-notes>
<corresp>Correspondence to: Paul Krack, Pavillon de Neurologie, CHU Grenoble, 38043 Grenoble, Cedex 9, France. E-mail:
<email>paul.krack@ujf-grenoble.fr</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub">
<month>4</month>
<year>2010</year>
</pub-date>
<pub-date pub-type="epub">
<day>17</day>
<month>3</month>
<year>2010</year>
</pub-date>
<volume>133</volume>
<issue>4</issue>
<fpage>1111</fpage>
<lpage>1127</lpage>
<history>
<date date-type="received">
<day>30</day>
<month>10</month>
<year>2009</year>
</date>
<date date-type="rev-recd">
<day>21</day>
<month>1</month>
<year>2010</year>
</date>
<date date-type="accepted">
<day>24</day>
<month>1</month>
<year>2010</year>
</date>
</history>
<permissions>
<copyright-statement>© The Author (2010). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org</copyright-statement>
<copyright-year>2010</copyright-year>
</permissions>
<abstract>
<p>Apathy has been reported to occur after subthalamic nucleus stimulation, a treatment of motor complications in advanced Parkinson’s disease. We carried out a prospective study of the occurrence of apathy and associated symptoms, predictors and mechanisms in the year following subthalamic stimulation. Dopamine agonist drugs were discontinued immediately after surgery and levodopa was markedly reduced within 2 weeks. Apathy and depression were assessed monthly, using the Starkstein apathy scale and the Beck Depression Inventory. Dopamine agonists were re-introduced if patients developed apathy or depression. Preoperative non-motor fluctuations were evaluated using the Ardouin Scale. Depression, apathy and anxiety were evaluated both on and off levodopa. Analysis of predictors of apathy was performed using a Cox proportional hazard model. Twelve patients who developed apathy and a control group of 13 patients who did not underwent [
<sup>11</sup>
C]-raclopride positron emission tomography scanning before and after oral intake of methylphenidate. In 63 patients with Parkinson’s disease treated with subthalamic stimulation, dopaminergic treatment was decreased by 82% after surgery. Apathy occurred after a mean of 4.7 (3.3–8.2) months in 34 patients and was reversible in half of these by the 12-month follow-up. Seventeen patients developed transient depression after 5.7 (4.7–9.3) months and these fell into the apathy group with one single exception. At baseline, fluctuations in depression, apathy and anxiety scores were greater in the group with apathy. Fluctuations in apathy, depression and anxiety ratings during a baseline levodopa challenge were also significant predictors of postoperative apathy in univariate analysis, but not motor and cognitive states or the level of reduction of dopaminergic medication. The multivariate model identified non-motor fluctuations in everyday life and anxiety score during the baseline levodopa challenge as two independent significant predictors of postoperative apathy. Without methylphenidate, [
<sup>11</sup>
C]-raclopride binding potential values were greater in apathetic patients bilaterally in the orbitofrontal, dorsolateral prefrontal, posterior cingulate and temporal cortices, left striatum and right amygdala, reflecting greater dopamine D2/D3 receptor density and/or reduced synaptic dopamine level in these areas. The variations of [
<sup>11</sup>
C]-raclopride binding potential values induced by methylphenidate were greater in non-apathetic patients in the left orbitofrontal cortex, dorsolateral prefrontal cortex, thalamus and internal globus pallidus and bilaterally in the anterior and posterior cingulate cortices, consistent with a more important capacity to release dopamine. Non-motor fluctuations are related to mesolimbic dopaminergic denervation. Apathy, depression and anxiety can occur after surgery as a delayed dopamine withdrawal syndrome. A varying extent of mesolimbic dopaminergic denervation and differences in dopaminergic treatment largely determine mood, anxiety and motivation in patients with Parkinson’s disease, contributing to different non-motor phenotypes.</p>
</abstract>
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<affiliation>2 CNRS, UMR 5229, Centre de Neurosciences Cognitives, 69003 Lyon, France</affiliation>
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<affiliation>4 INSERM, Unit 836, Grenoble Institut des Neurosciences, 38043 Grenoble, France</affiliation>
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<abstract>Apathy has been reported to occur after subthalamic nucleus stimulation, a treatment of motor complications in advanced Parkinsons disease. We carried out a prospective study of the occurrence of apathy and associated symptoms, predictors and mechanisms in the year following subthalamic stimulation. Dopamine agonist drugs were discontinued immediately after surgery and levodopa was markedly reduced within 2 weeks. Apathy and depression were assessed monthly, using the Starkstein apathy scale and the Beck Depression Inventory. Dopamine agonists were re-introduced if patients developed apathy or depression. Preoperative non-motor fluctuations were evaluated using the Ardouin Scale. Depression, apathy and anxiety were evaluated both on and off levodopa. Analysis of predictors of apathy was performed using a Cox proportional hazard model. Twelve patients who developed apathy and a control group of 13 patients who did not underwent [11C]-raclopride positron emission tomography scanning before and after oral intake of methylphenidate. In 63 patients with Parkinsons disease treated with subthalamic stimulation, dopaminergic treatment was decreased by 82 after surgery. Apathy occurred after a mean of 4.7 (3.38.2) months in 34 patients and was reversible in half of these by the 12-month follow-up. Seventeen patients developed transient depression after 5.7 (4.79.3) months and these fell into the apathy group with one single exception. At baseline, fluctuations in depression, apathy and anxiety scores were greater in the group with apathy. Fluctuations in apathy, depression and anxiety ratings during a baseline levodopa challenge were also significant predictors of postoperative apathy in univariate analysis, but not motor and cognitive states or the level of reduction of dopaminergic medication. The multivariate model identified non-motor fluctuations in everyday life and anxiety score during the baseline levodopa challenge as two independent significant predictors of postoperative apathy. Without methylphenidate, [11C]-raclopride binding potential values were greater in apathetic patients bilaterally in the orbitofrontal, dorsolateral prefrontal, posterior cingulate and temporal cortices, left striatum and right amygdala, reflecting greater dopamine D2/D3 receptor density and/or reduced synaptic dopamine level in these areas. The variations of [11C]-raclopride binding potential values induced by methylphenidate were greater in non-apathetic patients in the left orbitofrontal cortex, dorsolateral prefrontal cortex, thalamus and internal globus pallidus and bilaterally in the anterior and posterior cingulate cortices, consistent with a more important capacity to release dopamine. Non-motor fluctuations are related to mesolimbic dopaminergic denervation. Apathy, depression and anxiety can occur after surgery as a delayed dopamine withdrawal syndrome. A varying extent of mesolimbic dopaminergic denervation and differences in dopaminergic treatment largely determine mood, anxiety and motivation in patients with Parkinsons disease, contributing to different non-motor phenotypes.</abstract>
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<topic>Parkinsons disease</topic>
<topic>apathy</topic>
<topic>subthalamic nucleus stimulation</topic>
<topic>dopamine</topic>
<topic>depression</topic>
<topic>anxiety</topic>
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<date>2010</date>
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