Serveur d'exploration sur la maladie de Parkinson

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

Identifieur interne : 000407 ( Main/Curation ); précédent : 000406; suivant : 000408

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

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

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.

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DOI: 10.1093/brain/awq032

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<name sortKey="Seigneuret, Eric" sort="Seigneuret, Eric" uniqKey="Seigneuret E" first="Eric" last="Seigneuret">Eric Seigneuret</name>
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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="Reilhac, Anthonin" sort="Reilhac, Anthonin" uniqKey="Reilhac A" first="Anthonin" last="Reilhac">Anthonin Reilhac</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="Quesada, Jean Louis" sort="Quesada, Jean Louis" uniqKey="Quesada J" first="Jean-Louis" last="Quesada">Jean-Louis Quesada</name>
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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="Krack, Paul" sort="Krack, Paul" uniqKey="Krack P" first="Paul" last="Krack">Paul Krack</name>
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<author>
<name sortKey="Ardouin, Claire" sort="Ardouin, Claire" uniqKey="Ardouin C" first="Claire" last="Ardouin">Claire Ardouin</name>
<affiliation wicri:level="1">
<mods:affiliation>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
<country xml:lang="fr">France</country>
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<name sortKey="Lhomme, Eugnie" sort="Lhomme, Eugnie" uniqKey="Lhomme E" first="Eugnie" last="Lhomme">Eugnie Lhomme</name>
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</author>
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<wicri:regionArea>1 Universit Lyon I, Hospices Civils de Lyon, Hpital Neurologique Pierre Wertheimer, Service de Neurologie C, 69003 Lyon</wicri:regionArea>
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<affiliation wicri:level="1">
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</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>
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<wicri:regionArea>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble</wicri:regionArea>
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<country xml:lang="fr">France</country>
<wicri:regionArea>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble</wicri:regionArea>
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<affiliation wicri:level="1">
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</affiliation>
</author>
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<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>
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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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<wicri:regionArea>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble</wicri:regionArea>
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<wicri:regionArea>6 Neurosurgery Department, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble</wicri:regionArea>
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<author>
<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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<wicri:regionArea>7 Universit Lyon I; Hospices Civils de Lyon, Hpital Neurologique Pierre Wertheimer, Service de Neurochirurgie A, 69003 Lyon</wicri:regionArea>
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<wicri:regionArea>7 Universit Lyon I; Hospices Civils de Lyon, Hpital Neurologique Pierre Wertheimer, Service de Neurochirurgie A, 69003 Lyon</wicri:regionArea>
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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="Tremblay, Lon" sort="Tremblay, Lon" uniqKey="Tremblay L" first="Lon" last="Tremblay">Lon Tremblay</name>
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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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<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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<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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<wicri:regionArea>10 Clinatec, DRT/LETI, CEA-Grenoble, 38000 Grenoble</wicri:regionArea>
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<author>
<name sortKey="Broussolle, Emmanuel" sort="Broussolle, Emmanuel" uniqKey="Broussolle E" first="Emmanuel" last="Broussolle">Emmanuel Broussolle</name>
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<mods:affiliation>1 Universit Lyon I, Hospices Civils de Lyon, Hpital Neurologique Pierre Wertheimer, Service de Neurologie C, 69003 Lyon, France</mods:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>1 Universit Lyon I, Hospices Civils de Lyon, Hpital Neurologique Pierre Wertheimer, Service de Neurologie C, 69003 Lyon</wicri:regionArea>
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<wicri:regionArea>2 CNRS, UMR 5229, Centre de Neurosciences Cognitives, 69003 Lyon</wicri:regionArea>
</affiliation>
</author>
<author>
<name sortKey="Pollak, Pierre" sort="Pollak, Pierre" uniqKey="Pollak P" first="Pierre" last="Pollak">Pierre Pollak</name>
<affiliation wicri:level="1">
<mods:affiliation>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble, France</mods:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>3 Movement Disorder Unit, Department of Psychiatry and Neurology, CHU de Grenoble, Joseph Fourier University, 38043 Grenoble</wicri:regionArea>
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<author>
<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>
<country xml:lang="fr">France</country>
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</analytic>
<monogr></monogr>
<series>
<title level="j">Brain</title>
<idno type="ISSN">0006-8950</idno>
<idno type="eISSN">1460-2156</idno>
<imprint>
<publisher>Oxford University Press</publisher>
<date type="published" when="2010-04">2010-04</date>
<biblScope unit="volume">133</biblScope>
<biblScope unit="issue">4</biblScope>
<biblScope unit="page" from="1111">1111</biblScope>
<biblScope unit="page" to="1127">1127</biblScope>
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<idno type="ISSN">0006-8950</idno>
</series>
<idno type="istex">EAB99310FD3EC51E1AE0E5946614A8EF666A6094</idno>
<idno type="DOI">10.1093/brain/awq032</idno>
<idno type="ArticleID">awq032</idno>
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<idno type="ISSN">0006-8950</idno>
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<language ident="en">en</language>
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<front>
<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>
</front>
</TEI>
</record>

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