Movement Disorders (revue)

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Long‐term follow‐up of DYT1 dystonia patients treated by deep brain stimulation: An open‐label study

Identifieur interne : 001B97 ( Main/Curation ); précédent : 001B96; suivant : 001B98

Long‐term follow‐up of DYT1 dystonia patients treated by deep brain stimulation: An open‐label study

Auteurs : Laura Cif [France] ; Xavier Vasques [France] ; Victoria Gonzalez [France] ; Patrice Ravel [France] ; Brigitte Biolsi [France] ; Gwenaelle Collod-Beroud [France] ; Sylvie Tuffery-Giraud [France] ; Hassan Elfertit [France] ; Mireille Claustres [France] ; Philippe Coubes [France]

Source :

RBID : ISTEX:C9AE796F8705D2EBD0732ECEFED18513E9AB9CCD

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Abstract

Long‐term efficacy of internal globus pallidus (GPi) deep‐brain stimulation (DBS) in DYT1 dystonia and disease progression under DBS was studied. Twenty‐six patients of this open‐label study were divided into two groups: (A) with single bilateral GPi lead, (B) with a second bilateral GPi lead implanted owning to subsequent worsening of symptomatology. Dystonia was assessed with the Burke Scale. Appearance of new symptoms and distribution according to body region were recorded. In the whole cohort, significant decreases in motor and disability subscores (P < 0.0001) were observed at 1 year and maintained up to 10 years. Group B showed worsening of the symptoms. At 1 year, there were no significant differences between Groups A (without subsequent worsening) and B; at 5 years, a significant difference was found for motor and disability scores. Within Group B, four patients exhibited additional improvement after the second DBS surgery. In the 26 patients, significant difference (P = 0.001) was found between the number of body regions affected by dystonia preoperatively and over the whole follow‐up. DBS efficacy in DYT1 dystonia can be maintained up to 10 years (two patients). New symptoms appear with long‐term follow‐up and may improve with additional leads in a subgroup of patients. © 2009 Movement Disorder Society

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DOI: 10.1002/mds.22802

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ISTEX:C9AE796F8705D2EBD0732ECEFED18513E9AB9CCD

Le document en format XML

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<div type="abstract" xml:lang="en">Long‐term efficacy of internal globus pallidus (GPi) deep‐brain stimulation (DBS) in DYT1 dystonia and disease progression under DBS was studied. Twenty‐six patients of this open‐label study were divided into two groups: (A) with single bilateral GPi lead, (B) with a second bilateral GPi lead implanted owning to subsequent worsening of symptomatology. Dystonia was assessed with the Burke Scale. Appearance of new symptoms and distribution according to body region were recorded. In the whole cohort, significant decreases in motor and disability subscores (P < 0.0001) were observed at 1 year and maintained up to 10 years. Group B showed worsening of the symptoms. At 1 year, there were no significant differences between Groups A (without subsequent worsening) and B; at 5 years, a significant difference was found for motor and disability scores. Within Group B, four patients exhibited additional improvement after the second DBS surgery. In the 26 patients, significant difference (P = 0.001) was found between the number of body regions affected by dystonia preoperatively and over the whole follow‐up. DBS efficacy in DYT1 dystonia can be maintained up to 10 years (two patients). New symptoms appear with long‐term follow‐up and may improve with additional leads in a subgroup of patients. © 2009 Movement Disorder Society</div>
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<title xml:lang="en" level="a">Long-Term Follow-Up of DYT1 Dystonia Patients Treated by Deep Brain Stimulation: An Open-Label Study</title>
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<name sortKey="Coubes, Philippe" sort="Coubes, Philippe" uniqKey="Coubes P" first="Philippe" last="Coubes">Philippe Coubes</name>
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<series>
<title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
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<imprint>
<date when="2010">2010</date>
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<title level="j" type="main">Movement disorders</title>
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<term>Deep brain stimulation</term>
<term>Dystonia</term>
<term>Human</term>
<term>Long term</term>
<term>Nervous system diseases</term>
<term>Pallidum</term>
<term>Treatment</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Dystonie</term>
<term>Pathologie du système nerveux</term>
<term>Long terme</term>
<term>Homme</term>
<term>Traitement</term>
<term>Pallidum</term>
<term>Stimulation cérébrale profonde</term>
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<front>
<div type="abstract" xml:lang="en">Long-term efficacy of internal globus pallidus (GPi) deep-brain stimulation (DBS) in DYT1 dystonia and disease progression under DBS was studied. Twenty-six patients of this open-label study were divided into two groups: (A) with single bilateral GPi lead, (B) with a second bilateral GPi lead implanted owning to subsequent worsening of symptomatology. Dystonia was assessed with the Burke Scale. Appearance of new symptoms and distribution according to body region were recorded. In the whole cohort, significant decreases in motor and disability subscores (P < 0.0001) were observed at 1 year and maintained up to 10 years. Group B showed worsening of the symptoms. At I year, there were no significant differences between Groups A (without subsequent worsening) and B; at 5 years, a significant difference was found for motor and disability scores. Within Group B, four patients exhibited additional improvement after the second DBS surgery. In the 26 patients, significant difference (P = 0.001) was found between the number of body regions affected by dystonia preoperatively and over the whole follow-up. DBS efficacy in DYT1 dystonia can be maintained up to 10 years (two patients). New symptoms appear with long-term follow-up and may improve with additional leads in a subgroup of patients.</div>
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<name sortKey="Cif, Laura" sort="Cif, Laura" uniqKey="Cif L" first="Laura" last="Cif">Laura Cif</name>
</author>
<author>
<name sortKey="Vasques, Xavier" sort="Vasques, Xavier" uniqKey="Vasques X" first="Xavier" last="Vasques">Xavier Vasques</name>
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<name sortKey="Gonzalez, Victoria" sort="Gonzalez, Victoria" uniqKey="Gonzalez V" first="Victoria" last="Gonzalez">Victoria Gonzalez</name>
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<name sortKey="Ravel, Patrice" sort="Ravel, Patrice" uniqKey="Ravel P" first="Patrice" last="Ravel">Patrice Ravel</name>
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<name sortKey="Collod Eroud, Gwenaelle" sort="Collod Eroud, Gwenaelle" uniqKey="Collod Eroud G" first="Gwenaelle" last="Collod-Beroud">Gwenaelle Collod-Beroud</name>
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<name sortKey="Tuffery Iraud, Sylvie" sort="Tuffery Iraud, Sylvie" uniqKey="Tuffery Iraud S" first="Sylvie" last="Tuffery-Giraud">Sylvie Tuffery-Giraud</name>
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<name sortKey="Elfertit, Hassan" sort="Elfertit, Hassan" uniqKey="Elfertit H" first="Hassan" last="Elfertit">Hassan Elfertit</name>
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<name sortKey="Claustres, Mireille" sort="Claustres, Mireille" uniqKey="Claustres M" first="Mireille" last="Claustres">Mireille Claustres</name>
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<settlement type="city">Montpellier</settlement>
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<settlement type="city">Montpellier</settlement>
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<country xml:lang="fr">France</country>
<wicri:regionArea>CNRS UMR5048, Centre de Biochimie Structurale, Montpellier</wicri:regionArea>
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<settlement type="city">Montpellier</settlement>
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<wicri:regionArea>INSERM, U554, Montpellier</wicri:regionArea>
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<settlement type="city">Montpellier</settlement>
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<country xml:lang="fr">France</country>
<wicri:regionArea>Université de Montpellier 2, Montpellier</wicri:regionArea>
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<country xml:lang="fr">France</country>
<wicri:regionArea>CHRU Montpellier, Hôpital Gui de Chauliac, Service de Neurochirurgie, Montpellier</wicri:regionArea>
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<wicri:regionArea>Université de Montpellier 1, Montpellier</wicri:regionArea>
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<name sortKey="Tuffery Iraud, Sylvie" sort="Tuffery Iraud, Sylvie" uniqKey="Tuffery Iraud S" first="Sylvie" last="Tuffery-Giraud">Sylvie Tuffery-Giraud</name>
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<wicri:regionArea>Université de Montpellier 1, Montpellier</wicri:regionArea>
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<settlement type="city">Montpellier</settlement>
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<country xml:lang="fr">France</country>
<wicri:regionArea>INSERM, U827, Montpellier</wicri:regionArea>
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<settlement type="city">Montpellier</settlement>
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<name sortKey="Elfertit, Hassan" sort="Elfertit, Hassan" uniqKey="Elfertit H" first="Hassan" last="Elfertit">Hassan Elfertit</name>
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<country xml:lang="fr">France</country>
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<country xml:lang="fr">France</country>
<wicri:regionArea>Université de Montpellier 1, Montpellier</wicri:regionArea>
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<settlement type="city">Montpellier</settlement>
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<country xml:lang="fr">France</country>
<wicri:regionArea>INSERM, U827, Montpellier</wicri:regionArea>
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<settlement type="city">Montpellier</settlement>
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<country xml:lang="fr">France</country>
<wicri:regionArea>CHRU Montpellier, Hôpital Gui de Chauliac, Service de Neurochirurgie, Montpellier</wicri:regionArea>
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<country xml:lang="fr">France</country>
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<settlement type="city">Montpellier</settlement>
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<country xml:lang="fr">France</country>
<wicri:regionArea>Université de Montpellier 1, Montpellier</wicri:regionArea>
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<title level="j">Movement Disorders</title>
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<term>Aged</term>
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<term>DYT1 dystonia</term>
<term>Deep Brain Stimulation (methods)</term>
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<term>Dystonia (genetics)</term>
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<term>Dystonia</term>
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<term>Deep Brain Stimulation</term>
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<div type="abstract" xml:lang="en">Long‐term efficacy of internal globus pallidus (GPi) deep‐brain stimulation (DBS) in DYT1 dystonia and disease progression under DBS was studied. Twenty‐six patients of this open‐label study were divided into two groups: (A) with single bilateral GPi lead, (B) with a second bilateral GPi lead implanted owning to subsequent worsening of symptomatology. Dystonia was assessed with the Burke Scale. Appearance of new symptoms and distribution according to body region were recorded. In the whole cohort, significant decreases in motor and disability subscores (P < 0.0001) were observed at 1 year and maintained up to 10 years. Group B showed worsening of the symptoms. At 1 year, there were no significant differences between Groups A (without subsequent worsening) and B; at 5 years, a significant difference was found for motor and disability scores. Within Group B, four patients exhibited additional improvement after the second DBS surgery. In the 26 patients, significant difference (P = 0.001) was found between the number of body regions affected by dystonia preoperatively and over the whole follow‐up. DBS efficacy in DYT1 dystonia can be maintained up to 10 years (two patients). New symptoms appear with long‐term follow‐up and may improve with additional leads in a subgroup of patients. © 2009 Movement Disorder Society</div>
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