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Enhanced antisaccade abilities in children with Tourette syndrome: the Gap-effect Reversal

Tourette Syndrome (TS) is a childhood onset disorder of motor and vocal tics. The neural networks underlying TS overlap with those of saccade eye movements. Thus, deviations on saccadic tasks can provide important information about psychopathology of TS. Tourette syndrome often coexists with Attenti...

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Autores principales: Tajik-Parvinchi, Diana J., Sandor, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826111/
https://www.ncbi.nlm.nih.gov/pubmed/24312038
http://dx.doi.org/10.3389/fnhum.2013.00768
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author Tajik-Parvinchi, Diana J.
Sandor, Paul
author_facet Tajik-Parvinchi, Diana J.
Sandor, Paul
author_sort Tajik-Parvinchi, Diana J.
collection PubMed
description Tourette Syndrome (TS) is a childhood onset disorder of motor and vocal tics. The neural networks underlying TS overlap with those of saccade eye movements. Thus, deviations on saccadic tasks can provide important information about psychopathology of TS. Tourette syndrome often coexists with Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD). Hence, we manipulated various components of a saccade task to measure its effects on saccades of children with TS-only, TS+ADHD, TS+ADHD+OCD and healthy controls. Children looked toward (prosaccade) or in the opposite direction (antisaccade) of a peripheral target as soon as it appeared. The prosaccade and antisaccade tasks were presented in three conditions. In the Gap200 condition, the fixation dot disappeared 200 ms prior to the appearance of the peripheral target, In the Gap800 condition, the fixation dot disappeared 800 ms prior to the appearance of the peripheral target and in Overlap200 the fixation dot disappeared 200 ms after the appearance of the peripheral target. Fixation-offset manipulations had different effects on each group's antisaccades. The TS+ADHD+OCD group's antisaccade latencies and error rates remained relatively unchanged in the three conditions and displayed a pattern of eye movements that can be interpreted as enhanced. Alternatively, the TS+ADHD group displayed an overall pattern of longer saccadic latencies. Findings corroborate the hypothesis that the combination of tic disorder and ADHD results in unique behavioral profiles. It is plausible that a subgroup of children with TS develop an adaptive ability to control their tics which generalizes to enhanced volitional control of saccadic behavior as well. Supporting evidence and other findings are discussed.
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spelling pubmed-38261112013-12-05 Enhanced antisaccade abilities in children with Tourette syndrome: the Gap-effect Reversal Tajik-Parvinchi, Diana J. Sandor, Paul Front Hum Neurosci Neuroscience Tourette Syndrome (TS) is a childhood onset disorder of motor and vocal tics. The neural networks underlying TS overlap with those of saccade eye movements. Thus, deviations on saccadic tasks can provide important information about psychopathology of TS. Tourette syndrome often coexists with Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD). Hence, we manipulated various components of a saccade task to measure its effects on saccades of children with TS-only, TS+ADHD, TS+ADHD+OCD and healthy controls. Children looked toward (prosaccade) or in the opposite direction (antisaccade) of a peripheral target as soon as it appeared. The prosaccade and antisaccade tasks were presented in three conditions. In the Gap200 condition, the fixation dot disappeared 200 ms prior to the appearance of the peripheral target, In the Gap800 condition, the fixation dot disappeared 800 ms prior to the appearance of the peripheral target and in Overlap200 the fixation dot disappeared 200 ms after the appearance of the peripheral target. Fixation-offset manipulations had different effects on each group's antisaccades. The TS+ADHD+OCD group's antisaccade latencies and error rates remained relatively unchanged in the three conditions and displayed a pattern of eye movements that can be interpreted as enhanced. Alternatively, the TS+ADHD group displayed an overall pattern of longer saccadic latencies. Findings corroborate the hypothesis that the combination of tic disorder and ADHD results in unique behavioral profiles. It is plausible that a subgroup of children with TS develop an adaptive ability to control their tics which generalizes to enhanced volitional control of saccadic behavior as well. Supporting evidence and other findings are discussed. Frontiers Media S.A. 2013-11-13 /pmc/articles/PMC3826111/ /pubmed/24312038 http://dx.doi.org/10.3389/fnhum.2013.00768 Text en Copyright © 2013 Tajik-Parvinchi and Sandor. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Tajik-Parvinchi, Diana J.
Sandor, Paul
Enhanced antisaccade abilities in children with Tourette syndrome: the Gap-effect Reversal
title Enhanced antisaccade abilities in children with Tourette syndrome: the Gap-effect Reversal
title_full Enhanced antisaccade abilities in children with Tourette syndrome: the Gap-effect Reversal
title_fullStr Enhanced antisaccade abilities in children with Tourette syndrome: the Gap-effect Reversal
title_full_unstemmed Enhanced antisaccade abilities in children with Tourette syndrome: the Gap-effect Reversal
title_short Enhanced antisaccade abilities in children with Tourette syndrome: the Gap-effect Reversal
title_sort enhanced antisaccade abilities in children with tourette syndrome: the gap-effect reversal
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826111/
https://www.ncbi.nlm.nih.gov/pubmed/24312038
http://dx.doi.org/10.3389/fnhum.2013.00768
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