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Alien Hand, Restless Brain: Salience Network and Interhemispheric Connectivity Disruption Parallel Emergence and Extinction of Diagonistic Dyspraxia

Diagonistic dyspraxia (DD) is by far the most spectacular manifestation reported by sufferers of acute corpus callosum (CC) injury (so-called “split-brain”). In this form of alien hand syndrome, one hand acts at cross purposes with the other “against the patient’s will”. Although recent models view...

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Autores principales: Ridley, Ben, Beltramone, Marion, Wirsich, Jonathan, Le Troter, Arnaud, Tramoni, Eve, Aubert, Sandrine, Achard, Sophie, Ranjeva, Jean-Philippe, Guye, Maxime, Felician, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913492/
https://www.ncbi.nlm.nih.gov/pubmed/27378896
http://dx.doi.org/10.3389/fnhum.2016.00307
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author Ridley, Ben
Beltramone, Marion
Wirsich, Jonathan
Le Troter, Arnaud
Tramoni, Eve
Aubert, Sandrine
Achard, Sophie
Ranjeva, Jean-Philippe
Guye, Maxime
Felician, Olivier
author_facet Ridley, Ben
Beltramone, Marion
Wirsich, Jonathan
Le Troter, Arnaud
Tramoni, Eve
Aubert, Sandrine
Achard, Sophie
Ranjeva, Jean-Philippe
Guye, Maxime
Felician, Olivier
author_sort Ridley, Ben
collection PubMed
description Diagonistic dyspraxia (DD) is by far the most spectacular manifestation reported by sufferers of acute corpus callosum (CC) injury (so-called “split-brain”). In this form of alien hand syndrome, one hand acts at cross purposes with the other “against the patient’s will”. Although recent models view DD as a disorder of motor control, there is still little information regarding its neural underpinnings, due to widespread connectivity changes produced by CC insult, and the obstacle that non-volitional movements represent for task-based functional neuroimaging studies. Here, we studied patient AM, the first report of DD in patient with complete developmental CC agenesis. This unique case also offers the opportunity to study the resting-state connectomics of DD in the absence of diffuse changes subsequent to CC injury or surgery. AM developed DD following status epilepticus (SE) which resolved over a 2-year period. Whole brain functional connectivity (FC) was compared (Crawford-Howell [CH]) to 16 controls during the period of acute DD symptoms (Time 1) and after remission (Time 2). Whole brain graph theoretical models were also constructed and topological efficiency examined. At Time 1, disrupted FC was observed in inter-hemispheric and intra-hemispheric right edges, involving frontal superior and midline structures. Graph analysis indicated disruption of the efficiency of salience and right frontoparietal (FP) networks. At Time 2, after remission of diagnostic dyspraxia symptoms, FC and salience network changes had resolved. In sum, longitudinal analysis of connectivity in AM indicates that DD behaviors could result from disruption of systems that support the experience and control of volitional movements and the ability to generate appropriate behavioral responses to salient stimuli. This also raises the possibility that changes to large-scale functional architecture revealed by resting-state functional magnetic resonance imaging (fMRI) (rs-fMRI) may provide relevant information on the evolution of behavioral syndromes in addition to that provided by structural and task-based functional imaging.
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spelling pubmed-49134922016-07-04 Alien Hand, Restless Brain: Salience Network and Interhemispheric Connectivity Disruption Parallel Emergence and Extinction of Diagonistic Dyspraxia Ridley, Ben Beltramone, Marion Wirsich, Jonathan Le Troter, Arnaud Tramoni, Eve Aubert, Sandrine Achard, Sophie Ranjeva, Jean-Philippe Guye, Maxime Felician, Olivier Front Hum Neurosci Neuroscience Diagonistic dyspraxia (DD) is by far the most spectacular manifestation reported by sufferers of acute corpus callosum (CC) injury (so-called “split-brain”). In this form of alien hand syndrome, one hand acts at cross purposes with the other “against the patient’s will”. Although recent models view DD as a disorder of motor control, there is still little information regarding its neural underpinnings, due to widespread connectivity changes produced by CC insult, and the obstacle that non-volitional movements represent for task-based functional neuroimaging studies. Here, we studied patient AM, the first report of DD in patient with complete developmental CC agenesis. This unique case also offers the opportunity to study the resting-state connectomics of DD in the absence of diffuse changes subsequent to CC injury or surgery. AM developed DD following status epilepticus (SE) which resolved over a 2-year period. Whole brain functional connectivity (FC) was compared (Crawford-Howell [CH]) to 16 controls during the period of acute DD symptoms (Time 1) and after remission (Time 2). Whole brain graph theoretical models were also constructed and topological efficiency examined. At Time 1, disrupted FC was observed in inter-hemispheric and intra-hemispheric right edges, involving frontal superior and midline structures. Graph analysis indicated disruption of the efficiency of salience and right frontoparietal (FP) networks. At Time 2, after remission of diagnostic dyspraxia symptoms, FC and salience network changes had resolved. In sum, longitudinal analysis of connectivity in AM indicates that DD behaviors could result from disruption of systems that support the experience and control of volitional movements and the ability to generate appropriate behavioral responses to salient stimuli. This also raises the possibility that changes to large-scale functional architecture revealed by resting-state functional magnetic resonance imaging (fMRI) (rs-fMRI) may provide relevant information on the evolution of behavioral syndromes in addition to that provided by structural and task-based functional imaging. Frontiers Media S.A. 2016-06-20 /pmc/articles/PMC4913492/ /pubmed/27378896 http://dx.doi.org/10.3389/fnhum.2016.00307 Text en Copyright © 2016 Ridley, Beltramone, Wirsich, Le Troter, Tramoni, Aubert, Achard, Ranjeva, Guye and Felician. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and 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
Ridley, Ben
Beltramone, Marion
Wirsich, Jonathan
Le Troter, Arnaud
Tramoni, Eve
Aubert, Sandrine
Achard, Sophie
Ranjeva, Jean-Philippe
Guye, Maxime
Felician, Olivier
Alien Hand, Restless Brain: Salience Network and Interhemispheric Connectivity Disruption Parallel Emergence and Extinction of Diagonistic Dyspraxia
title Alien Hand, Restless Brain: Salience Network and Interhemispheric Connectivity Disruption Parallel Emergence and Extinction of Diagonistic Dyspraxia
title_full Alien Hand, Restless Brain: Salience Network and Interhemispheric Connectivity Disruption Parallel Emergence and Extinction of Diagonistic Dyspraxia
title_fullStr Alien Hand, Restless Brain: Salience Network and Interhemispheric Connectivity Disruption Parallel Emergence and Extinction of Diagonistic Dyspraxia
title_full_unstemmed Alien Hand, Restless Brain: Salience Network and Interhemispheric Connectivity Disruption Parallel Emergence and Extinction of Diagonistic Dyspraxia
title_short Alien Hand, Restless Brain: Salience Network and Interhemispheric Connectivity Disruption Parallel Emergence and Extinction of Diagonistic Dyspraxia
title_sort alien hand, restless brain: salience network and interhemispheric connectivity disruption parallel emergence and extinction of diagonistic dyspraxia
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913492/
https://www.ncbi.nlm.nih.gov/pubmed/27378896
http://dx.doi.org/10.3389/fnhum.2016.00307
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