Vergence deficits in patients with cerebellar lesions
The cerebellum is part of the cortico–ponto–cerebellar circuit for conjugate eye movements. Recent animal data suggest an additional role of the cerebellum for the control of binocular alignment and disconjugate, i.e. vergence eye movements. The latter is separated into two different components: fas...
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Veröffentlicht in: | Brain (London, England : 1878) England : 1878), 2009-01, Vol.132 (1), p.103-115 |
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description | The cerebellum is part of the cortico–ponto–cerebellar circuit for conjugate eye movements. Recent animal data suggest an additional role of the cerebellum for the control of binocular alignment and disconjugate, i.e. vergence eye movements. The latter is separated into two different components: fast vergence (to step targets) and slow vergence (to ramp and sinusoidal targets). The aim of this study was to investigate whether circumscribed cerebellar lesions affect these dynamic vergence eye movements. Disconjugate fast and slow vergence, conjugate smooth pursuit and saccades were binocularly recorded by a scleral search coil system in 20 patients with acute cerebellar lesions (all ischemic strokes except for one) and 20 age-matched healthy controls. Patients showed impairment of slow vergence while fast vergence was unaffected. Slow vergence gain to sinusoidal targets was significantly reduced, both in convergence and divergence direction. Divergence but not convergence velocity to ramp targets was reduced. Conjugate smooth pursuit eye movements to sinusoidal and to step-ramp targets were impaired. Patients had saccadic hypometria. All defects were particularly expressed in patients with vermis lesions. In contrast to recent animal data fast vergence was not impaired in any of our patient subgroups. We conclude that (i) the human cerebellum, in particular the vermis, is involved in the processing of dynamic vergence eye movements and (ii) cerebellar lesions elicit dissociable effects on fast and slow vergence. |
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Recent animal data suggest an additional role of the cerebellum for the control of binocular alignment and disconjugate, i.e. vergence eye movements. The latter is separated into two different components: fast vergence (to step targets) and slow vergence (to ramp and sinusoidal targets). The aim of this study was to investigate whether circumscribed cerebellar lesions affect these dynamic vergence eye movements. Disconjugate fast and slow vergence, conjugate smooth pursuit and saccades were binocularly recorded by a scleral search coil system in 20 patients with acute cerebellar lesions (all ischemic strokes except for one) and 20 age-matched healthy controls. Patients showed impairment of slow vergence while fast vergence was unaffected. Slow vergence gain to sinusoidal targets was significantly reduced, both in convergence and divergence direction. Divergence but not convergence velocity to ramp targets was reduced. Conjugate smooth pursuit eye movements to sinusoidal and to step-ramp targets were impaired. Patients had saccadic hypometria. All defects were particularly expressed in patients with vermis lesions. In contrast to recent animal data fast vergence was not impaired in any of our patient subgroups. We conclude that (i) the human cerebellum, in particular the vermis, is involved in the processing of dynamic vergence eye movements and (ii) cerebellar lesions elicit dissociable effects on fast and slow vergence.</description><identifier>ISSN: 0006-8950</identifier><identifier>EISSN: 1460-2156</identifier><identifier>DOI: 10.1093/brain/awn306</identifier><identifier>PMID: 19036765</identifier><identifier>CODEN: BRAIAK</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Animals ; Biological and medical sciences ; Brain ; Brain Mapping - methods ; Cerebellar Neoplasms - complications ; Cerebellum - blood supply ; Cerebellum - physiopathology ; Cerebral Infarction - complications ; Cerebral Infarction - pathology ; Cognitive Processes ; Control Groups ; Convergence, Ocular ; divergence ; Eye Movement Measurements ; Eye Movements ; fast vergence ; Female ; Human Body ; Humans ; Magnetic Resonance Imaging - methods ; Male ; Medical sciences ; Middle Aged ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Neurological Impairments ; Neurology ; Ocular Motility Disorders - etiology ; Ocular Motility Disorders - physiopathology ; Patients ; Pursuit, Smooth ; Saccades ; slow vergence ; vermis</subject><ispartof>Brain (London, England : 1878), 2009-01, Vol.132 (1), p.103-115</ispartof><rights>The Author (2008). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org 2008</rights><rights>2009 INIST-CNRS</rights><rights>The Author (2008). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c506t-f0572236c23e6493ae8927269dbe3e5de160f80421563a74cba1bfd325d197983</citedby><cites>FETCH-LOGICAL-c506t-f0572236c23e6493ae8927269dbe3e5de160f80421563a74cba1bfd325d197983</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttp://eric.ed.gov/ERICWebPortal/detail?accno=EJ839795$$DView record in ERIC$$Hfree_for_read</backlink><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21093602$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19036765$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sander, T.</creatorcontrib><creatorcontrib>Sprenger, A.</creatorcontrib><creatorcontrib>Neumann, G.</creatorcontrib><creatorcontrib>Machner, B.</creatorcontrib><creatorcontrib>Gottschalk, S.</creatorcontrib><creatorcontrib>Rambold, H.</creatorcontrib><creatorcontrib>Helmchen, C.</creatorcontrib><title>Vergence deficits in patients with cerebellar lesions</title><title>Brain (London, England : 1878)</title><addtitle>Brain</addtitle><description>The cerebellum is part of the cortico–ponto–cerebellar circuit for conjugate eye movements. Recent animal data suggest an additional role of the cerebellum for the control of binocular alignment and disconjugate, i.e. vergence eye movements. The latter is separated into two different components: fast vergence (to step targets) and slow vergence (to ramp and sinusoidal targets). The aim of this study was to investigate whether circumscribed cerebellar lesions affect these dynamic vergence eye movements. Disconjugate fast and slow vergence, conjugate smooth pursuit and saccades were binocularly recorded by a scleral search coil system in 20 patients with acute cerebellar lesions (all ischemic strokes except for one) and 20 age-matched healthy controls. Patients showed impairment of slow vergence while fast vergence was unaffected. Slow vergence gain to sinusoidal targets was significantly reduced, both in convergence and divergence direction. Divergence but not convergence velocity to ramp targets was reduced. Conjugate smooth pursuit eye movements to sinusoidal and to step-ramp targets were impaired. Patients had saccadic hypometria. All defects were particularly expressed in patients with vermis lesions. In contrast to recent animal data fast vergence was not impaired in any of our patient subgroups. We conclude that (i) the human cerebellum, in particular the vermis, is involved in the processing of dynamic vergence eye movements and (ii) cerebellar lesions elicit dissociable effects on fast and slow vergence.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain</subject><subject>Brain Mapping - methods</subject><subject>Cerebellar Neoplasms - complications</subject><subject>Cerebellum - blood supply</subject><subject>Cerebellum - physiopathology</subject><subject>Cerebral Infarction - complications</subject><subject>Cerebral Infarction - pathology</subject><subject>Cognitive Processes</subject><subject>Control Groups</subject><subject>Convergence, Ocular</subject><subject>divergence</subject><subject>Eye Movement Measurements</subject><subject>Eye Movements</subject><subject>fast vergence</subject><subject>Female</subject><subject>Human Body</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>Neurological Impairments</subject><subject>Neurology</subject><subject>Ocular Motility Disorders - etiology</subject><subject>Ocular Motility Disorders - physiopathology</subject><subject>Patients</subject><subject>Pursuit, Smooth</subject><subject>Saccades</subject><subject>slow vergence</subject><subject>vermis</subject><issn>0006-8950</issn><issn>1460-2156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0E1r1UAUBuBBFHtb3bkUCUJ1Y-yZ78xSSrVqQfCjvbgZJpMTnZo7uc4kVP-9iblcwY2u5sB5eDnzEvKAwnMKhp_UyYV44m4iB3WLrKhQUDIq1W2yAgBVVkbCATnM-RqACs7UXXJADXCllVwReYnpC0aPRYNt8GHIRYjF1g0B4zTfhOFr4TFhjV3nUtFhDn3M98id1nUZ7-_eI_Lp5dnH0_Py4t2r16cvLkovQQ1lC1IzxpVnHJUw3GFlmGbKNDVylA1SBW0FYj6XOy187WjdNpzJhhptKn5Eniy529R_HzEPdhOyn0-J2I_ZKlUJaf4DMuCm0lRO8PFf8LofU5w-YamRQshK6gk9W5BPfc4JW7tNYePST0vBzqXb36XbpfSJP9pljvUGmz941_IEjnfAZe-6NrnoQ947NkcqYJN7uDhMwe_XZ28qPrUxxzxd1v24_ddF5SJDHvDH3rr0zSrNtbTn68_2g7h8f7V-e2XX_Beaia9y</recordid><startdate>200901</startdate><enddate>200901</enddate><creator>Sander, T.</creator><creator>Sprenger, A.</creator><creator>Neumann, G.</creator><creator>Machner, B.</creator><creator>Gottschalk, S.</creator><creator>Rambold, H.</creator><creator>Helmchen, C.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>7SW</scope><scope>BJH</scope><scope>BNH</scope><scope>BNI</scope><scope>BNJ</scope><scope>BNO</scope><scope>ERI</scope><scope>PET</scope><scope>REK</scope><scope>WWN</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200901</creationdate><title>Vergence deficits in patients with cerebellar lesions</title><author>Sander, T. ; Sprenger, A. ; Neumann, G. ; Machner, B. ; Gottschalk, S. ; Rambold, H. ; Helmchen, C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c506t-f0572236c23e6493ae8927269dbe3e5de160f80421563a74cba1bfd325d197983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brain</topic><topic>Brain Mapping - methods</topic><topic>Cerebellar Neoplasms - complications</topic><topic>Cerebellum - blood supply</topic><topic>Cerebellum - physiopathology</topic><topic>Cerebral Infarction - complications</topic><topic>Cerebral Infarction - pathology</topic><topic>Cognitive Processes</topic><topic>Control Groups</topic><topic>Convergence, Ocular</topic><topic>divergence</topic><topic>Eye Movement Measurements</topic><topic>Eye Movements</topic><topic>fast vergence</topic><topic>Female</topic><topic>Human Body</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. 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Recent animal data suggest an additional role of the cerebellum for the control of binocular alignment and disconjugate, i.e. vergence eye movements. The latter is separated into two different components: fast vergence (to step targets) and slow vergence (to ramp and sinusoidal targets). The aim of this study was to investigate whether circumscribed cerebellar lesions affect these dynamic vergence eye movements. Disconjugate fast and slow vergence, conjugate smooth pursuit and saccades were binocularly recorded by a scleral search coil system in 20 patients with acute cerebellar lesions (all ischemic strokes except for one) and 20 age-matched healthy controls. Patients showed impairment of slow vergence while fast vergence was unaffected. Slow vergence gain to sinusoidal targets was significantly reduced, both in convergence and divergence direction. Divergence but not convergence velocity to ramp targets was reduced. Conjugate smooth pursuit eye movements to sinusoidal and to step-ramp targets were impaired. Patients had saccadic hypometria. All defects were particularly expressed in patients with vermis lesions. In contrast to recent animal data fast vergence was not impaired in any of our patient subgroups. We conclude that (i) the human cerebellum, in particular the vermis, is involved in the processing of dynamic vergence eye movements and (ii) cerebellar lesions elicit dissociable effects on fast and slow vergence.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>19036765</pmid><doi>10.1093/brain/awn306</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Adult Aged Aged, 80 and over Animals Biological and medical sciences Brain Brain Mapping - methods Cerebellar Neoplasms - complications Cerebellum - blood supply Cerebellum - physiopathology Cerebral Infarction - complications Cerebral Infarction - pathology Cognitive Processes Control Groups Convergence, Ocular divergence Eye Movement Measurements Eye Movements fast vergence Female Human Body Humans Magnetic Resonance Imaging - methods Male Medical sciences Middle Aged Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis Neurological Impairments Neurology Ocular Motility Disorders - etiology Ocular Motility Disorders - physiopathology Patients Pursuit, Smooth Saccades slow vergence vermis |
title | Vergence deficits in patients with cerebellar lesions |
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