Vestibular evoked myogenic potentials are intact in cervical dystonia
Identifieur interne : 001916 ( Main/Curation ); précédent : 001915; suivant : 001917Vestibular evoked myogenic potentials are intact in cervical dystonia
Auteurs : Sally M. Rosengren [Australie] ; James G. Colebatch [Australie]Source :
- Movement Disorders [ 0885-3185 ] ; 2010-12-15.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Adult, Aged, Analysis of Variance, Botulinum Toxins, Type A (therapeutic use), Dystonia, Evoked potential, Eye Movements (physiology), Female, Humans, Male, Middle Aged, Neck Muscles (drug effects), Neck Muscles (physiopathology), Nervous system diseases, Neuromuscular Agents (therapeutic use), Torticollis, Torticollis (physiopathology), Torticollis (therapy), VEMP, Vestibular Evoked Myogenic Potentials (drug effects), Vestibular Evoked Myogenic Potentials (physiology), oVEMP, subjective visual vertical, torticollis, vestibular.
- MESH :
- chemical , therapeutic use : Botulinum Toxins, Type A, Neuromuscular Agents.
- drug effects : Neck Muscles, Vestibular Evoked Myogenic Potentials.
- physiology : Eye Movements, Vestibular Evoked Myogenic Potentials.
- physiopathology : Neck Muscles, Torticollis.
- therapy : Torticollis.
- Adult, Aged, Analysis of Variance, Female, Humans, Male, Middle Aged.
Abstract
Vestibular dysfunction has been reported in patients with cervical dystonia (CD), but it is still unclear whether the abnormalities occur as part of the CD syndrome or whether they arise from the abnormal posture and movement of the head. We compared vestibular‐evoked myogenic potentials (VEMPs) recorded from the affected neck muscles (i.e., cervical VEMPs) with those recorded from muscles unaffected by the dystonia, the extraocular muscles (i.e., ocular VEMPs). We compared 21 patients and age‐matched normal controls to investigate whether these short‐latency reflexes are altered in CD. We also measured subjective visual horizontal (SVH). Seven patients had not received botulinum toxin treatment (naïve group), 10 were receiving regular injections (treatment group), and four had previously received treatment but had developed antibodies (antibody group). Both cervical and ocular VEMPs were present in the majority of patients and controls. For both reflexes, there were no significant differences between stimulation of the two sides of the head, between the treatment groups, or between the patients and controls. There was also no difference in degree of deviation of SVH between the groups. Our results showed that VEMPs can be reliably recorded from both the neck and extraocular muscles in patients with CD, even after long disease or treatment durations, and provide evidence for intact short‐latency vestibular reflexes in CD. © 2010 Movement Disorder Society.
Url:
DOI: 10.1002/mds.23422
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We compared vestibular‐evoked myogenic potentials (VEMPs) recorded from the affected neck muscles (i.e., cervical VEMPs) with those recorded from muscles unaffected by the dystonia, the extraocular muscles (i.e., ocular VEMPs). We compared 21 patients and age‐matched normal controls to investigate whether these short‐latency reflexes are altered in CD. We also measured subjective visual horizontal (SVH). Seven patients had not received botulinum toxin treatment (naïve group), 10 were receiving regular injections (treatment group), and four had previously received treatment but had developed antibodies (antibody group). Both cervical and ocular VEMPs were present in the majority of patients and controls. For both reflexes, there were no significant differences between stimulation of the two sides of the head, between the treatment groups, or between the patients and controls. There was also no difference in degree of deviation of SVH between the groups. Our results showed that VEMPs can be reliably recorded from both the neck and extraocular muscles in patients with CD, even after long disease or treatment durations, and provide evidence for intact short‐latency vestibular reflexes in CD. © 2010 Movement Disorder Society.</div></front></TEI><double idat="0885-3185:2010:Rosengren S:vestibular:evoked:myogenic"><INIST><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Vestibular Evoked Myogenic Potentials are Intact in Cervical Dystonia</title><author><name sortKey="Rosengren, Sally M" sort="Rosengren, Sally M" uniqKey="Rosengren S" first="Sally M." last="Rosengren">Sally M. Rosengren</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Prince of Wales Clinical School and Neuroscience Research Australia, University of New South Wales, Randwick</s1><s2>Sydney, New South Wales</s2><s3>AUS</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14><country>Australie</country><wicri:noRegion>Sydney, New South Wales</wicri:noRegion></affiliation></author><author><name sortKey="Colebatch, James G" sort="Colebatch, James G" uniqKey="Colebatch J" first="James G." last="Colebatch">James G. Colebatch</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Prince of Wales Clinical School and Neuroscience Research Australia, University of New South Wales, Randwick</s1><s2>Sydney, New South Wales</s2><s3>AUS</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14><country>Australie</country><wicri:noRegion>Sydney, New South Wales</wicri:noRegion></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">INIST</idno><idno type="inist">11-0065126</idno><date when="2010">2010</date><idno type="stanalyst">PASCAL 11-0065126 INIST</idno><idno type="RBID">Pascal:11-0065126</idno><idno type="wicri:Area/PascalFrancis/Corpus">000773</idno><idno type="wicri:Area/PascalFrancis/Curation">002545</idno><idno type="wicri:Area/PascalFrancis/Checkpoint">000757</idno><idno type="wicri:doubleKey">0885-3185:2010:Rosengren S:vestibular:evoked:myogenic</idno><idno type="wicri:Area/Main/Merge">002344</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Vestibular Evoked Myogenic Potentials are Intact in Cervical Dystonia</title><author><name sortKey="Rosengren, Sally M" sort="Rosengren, Sally M" uniqKey="Rosengren S" first="Sally M." last="Rosengren">Sally M. Rosengren</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Prince of Wales Clinical School and Neuroscience Research Australia, University of New South Wales, Randwick</s1><s2>Sydney, New South Wales</s2><s3>AUS</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14><country>Australie</country><wicri:noRegion>Sydney, New South Wales</wicri:noRegion></affiliation></author><author><name sortKey="Colebatch, James G" sort="Colebatch, James G" uniqKey="Colebatch J" first="James G." last="Colebatch">James G. Colebatch</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Prince of Wales Clinical School and Neuroscience Research Australia, University of New South Wales, Randwick</s1><s2>Sydney, New South Wales</s2><s3>AUS</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14><country>Australie</country><wicri:noRegion>Sydney, New South Wales</wicri:noRegion></affiliation></author></analytic><series><title level="j" type="main">Movement disorders</title><title level="j" type="abbreviated">Mov. disord.</title><idno type="ISSN">0885-3185</idno><imprint><date when="2010">2010</date></imprint></series></biblStruct></sourceDesc><seriesStmt><title level="j" type="main">Movement disorders</title><title level="j" type="abbreviated">Mov. disord.</title><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Dystonia</term><term>Evoked potential</term><term>Nervous system diseases</term><term>Torticollis</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Dystonie</term><term>Torticolis</term><term>Pathologie du système nerveux</term><term>Potentiel évoqué</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Vestibular dysfunction has been reported in patients with cervical dystonia (CD), but it is still unclear whether the abnormalities occur as part of the CD syndrome or whether they arise from the abnormal posture and movement of the head. We compared vestibular-evoked myogenic potentials (VEMPs) recorded from the affected neck muscles (i.e., cervical VEMPs) with those recorded from muscles unaffected by the dystonia, the extraocular muscles (i.e., ocular VEMPs). We compared 21 patients and age-matched normal controls to investigate whether these short-latency reflexes are altered in CD. We also measured subjective visual horizontal (SVH). Seven patients had not received botulinum toxin treatment (naïve group), 10 were receiving regular injections (treatment group), and four had previously received treatment but had developed antibodies (antibody group). Both cervical and ocular VEMPs were present in the majority of patients and controls. For both reflexes, there were no significant differences between stimulation of the two sides of the head, between the treatment groups, or between the patients and controls. There was also no difference in degree of deviation of SVH between the groups. Our results showed that VEMPs can be reliably recorded from both the neck and extraocular muscles in patients with CD, even after long disease or treatment durations, and provide evidence for intact short-latency vestibular reflexes in CD.</div></front></TEI></INIST><ISTEX><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Vestibular evoked myogenic potentials are intact in cervical dystonia</title><author><name sortKey="Rosengren, Sally M" sort="Rosengren, Sally M" uniqKey="Rosengren S" first="Sally M." last="Rosengren">Sally M. Rosengren</name></author><author><name sortKey="Colebatch, James G" sort="Colebatch, James G" uniqKey="Colebatch J" first="James G." last="Colebatch">James G. Colebatch</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:EB7FFFDF0B4717E6438202F6305EDCB0500BE785</idno><date when="2010" year="2010">2010</date><idno type="doi">10.1002/mds.23422</idno><idno type="url">https://api.istex.fr/document/EB7FFFDF0B4717E6438202F6305EDCB0500BE785/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">000A97</idno><idno type="wicri:Area/Istex/Curation">000A97</idno><idno type="wicri:Area/Istex/Checkpoint">000595</idno><idno type="wicri:doubleKey">0885-3185:2010:Rosengren S:vestibular:evoked:myogenic</idno><idno type="wicri:source">PubMed</idno><idno type="RBID">pubmed:20960477</idno><idno type="wicri:Area/PubMed/Corpus">001503</idno><idno type="wicri:Area/PubMed/Curation">001503</idno><idno type="wicri:Area/PubMed/Checkpoint">001523</idno><idno type="wicri:Area/Ncbi/Merge">002F14</idno><idno type="wicri:Area/Ncbi/Curation">002F14</idno><idno type="wicri:Area/Ncbi/Checkpoint">002F14</idno><idno type="wicri:Area/Main/Merge">001D52</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Vestibular evoked myogenic potentials are intact in cervical dystonia</title><author><name sortKey="Rosengren, Sally M" sort="Rosengren, Sally M" uniqKey="Rosengren S" first="Sally M." last="Rosengren">Sally M. Rosengren</name><affiliation wicri:level="1"><country xml:lang="fr">Australie</country><wicri:regionArea>Department of Neurology, Prince of Wales Clinical School and Neuroscience Research Australia, University of New South Wales, Randwick, Sydney, New South Wales</wicri:regionArea><wicri:noRegion>New South Wales</wicri:noRegion></affiliation></author><author><name sortKey="Colebatch, James G" sort="Colebatch, James G" uniqKey="Colebatch J" first="James G." last="Colebatch">James G. Colebatch</name><affiliation wicri:level="1"><country xml:lang="fr">Australie</country><wicri:regionArea>Department of Neurology, Prince of Wales Clinical School and Neuroscience Research Australia, University of New South Wales, Randwick, Sydney, New South Wales</wicri:regionArea><wicri:noRegion>New South Wales</wicri:noRegion></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</title><title level="j" type="abbrev">Mov. Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="2010-12-15">2010-12-15</date><biblScope unit="vol">25</biblScope><biblScope unit="issue">16</biblScope><biblScope unit="page" from="2845">2845</biblScope><biblScope unit="page" to="2853">2853</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">EB7FFFDF0B4717E6438202F6305EDCB0500BE785</idno><idno type="DOI">10.1002/mds.23422</idno><idno type="ArticleID">MDS23422</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Aged</term><term>Analysis of Variance</term><term>Botulinum Toxins, Type A (therapeutic use)</term><term>Eye Movements (physiology)</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Neck Muscles (drug effects)</term><term>Neck Muscles (physiopathology)</term><term>Neuromuscular Agents (therapeutic use)</term><term>Torticollis (physiopathology)</term><term>Torticollis (therapy)</term><term>VEMP</term><term>Vestibular Evoked Myogenic Potentials (drug effects)</term><term>Vestibular Evoked Myogenic Potentials (physiology)</term><term>oVEMP</term><term>subjective visual vertical</term><term>torticollis</term><term>vestibular</term></keywords><keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Botulinum Toxins, Type A</term><term>Neuromuscular Agents</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Neck Muscles</term><term>Vestibular Evoked Myogenic Potentials</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Eye Movements</term><term>Vestibular Evoked Myogenic Potentials</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Neck Muscles</term><term>Torticollis</term></keywords><keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Torticollis</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Aged</term><term>Analysis of Variance</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Vestibular dysfunction has been reported in patients with cervical dystonia (CD), but it is still unclear whether the abnormalities occur as part of the CD syndrome or whether they arise from the abnormal posture and movement of the head. We compared vestibular‐evoked myogenic potentials (VEMPs) recorded from the affected neck muscles (i.e., cervical VEMPs) with those recorded from muscles unaffected by the dystonia, the extraocular muscles (i.e., ocular VEMPs). We compared 21 patients and age‐matched normal controls to investigate whether these short‐latency reflexes are altered in CD. We also measured subjective visual horizontal (SVH). Seven patients had not received botulinum toxin treatment (naïve group), 10 were receiving regular injections (treatment group), and four had previously received treatment but had developed antibodies (antibody group). Both cervical and ocular VEMPs were present in the majority of patients and controls. For both reflexes, there were no significant differences between stimulation of the two sides of the head, between the treatment groups, or between the patients and controls. There was also no difference in degree of deviation of SVH between the groups. Our results showed that VEMPs can be reliably recorded from both the neck and extraocular muscles in patients with CD, even after long disease or treatment durations, and provide evidence for intact short‐latency vestibular reflexes in CD. © 2010 Movement Disorder Society.</div></front></TEI></ISTEX></double></record>Pour manipuler ce document sous Unix (Dilib)
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