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Measures of metabolism and complexity in the brain of patients with disorders of consciousness

BACKGROUND: Making an accurate diagnosis in patients with disorders of consciousness remains challenging. (18)F-fluorodeoxyglucose (FDG)–PET has been validated as a diagnostic tool in this population, and allows identifying unresponsive patients with a capacity for consciousness. In parallel, the pe...

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Autores principales: Bodart, Olivier, Gosseries, Olivia, Wannez, Sarah, Thibaut, Aurore, Annen, Jitka, Boly, Melanie, Rosanova, Mario, Casali, Adenauer G., Casarotto, Silvia, Tononi, Giulio, Massimini, Marcello, Laureys, Steven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318348/
https://www.ncbi.nlm.nih.gov/pubmed/28239544
http://dx.doi.org/10.1016/j.nicl.2017.02.002
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author Bodart, Olivier
Gosseries, Olivia
Wannez, Sarah
Thibaut, Aurore
Annen, Jitka
Boly, Melanie
Rosanova, Mario
Casali, Adenauer G.
Casarotto, Silvia
Tononi, Giulio
Massimini, Marcello
Laureys, Steven
author_facet Bodart, Olivier
Gosseries, Olivia
Wannez, Sarah
Thibaut, Aurore
Annen, Jitka
Boly, Melanie
Rosanova, Mario
Casali, Adenauer G.
Casarotto, Silvia
Tononi, Giulio
Massimini, Marcello
Laureys, Steven
author_sort Bodart, Olivier
collection PubMed
description BACKGROUND: Making an accurate diagnosis in patients with disorders of consciousness remains challenging. (18)F-fluorodeoxyglucose (FDG)–PET has been validated as a diagnostic tool in this population, and allows identifying unresponsive patients with a capacity for consciousness. In parallel, the perturbational complexity index (PCI), a new measure based on the analysis of the electroencephalographic response to transcranial magnetic stimulation, has also been suggested as a tool to distinguish between unconscious and conscious states. The aim of the study was to cross-validate FDG–PET and PCI, and to identify signs of consciousness in otherwise unresponsive patients. METHODS: We jointly applied the Coma Recovery Scale-Revised, FDG–PET and PCI to assess 24 patients with non-acute disorders of consciousness or locked-in syndrome (13 male; 19–54 years old; 12 traumatic; 9 unresponsive wakefulness syndrome, 11 minimally conscious state; 2 emergence from the minimally conscious state, and 2 locked-in syndrome). RESULTS: FDG–PET and PCI provided congruent results in 22 patients, regardless of their behavioural diagnosis. Notably, FDG–PET and PCI revealed preserved metabolic rates and high complexity levels in four patients who were behaviourally unresponsive. CONCLUSION: We propose that jointly measuring the metabolic activity and the electrophysiological complexity of cortical circuits is a useful complement to the diagnosis and stratification of patients with disorders of consciousness.
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spelling pubmed-53183482017-02-26 Measures of metabolism and complexity in the brain of patients with disorders of consciousness Bodart, Olivier Gosseries, Olivia Wannez, Sarah Thibaut, Aurore Annen, Jitka Boly, Melanie Rosanova, Mario Casali, Adenauer G. Casarotto, Silvia Tononi, Giulio Massimini, Marcello Laureys, Steven Neuroimage Clin Regular Article BACKGROUND: Making an accurate diagnosis in patients with disorders of consciousness remains challenging. (18)F-fluorodeoxyglucose (FDG)–PET has been validated as a diagnostic tool in this population, and allows identifying unresponsive patients with a capacity for consciousness. In parallel, the perturbational complexity index (PCI), a new measure based on the analysis of the electroencephalographic response to transcranial magnetic stimulation, has also been suggested as a tool to distinguish between unconscious and conscious states. The aim of the study was to cross-validate FDG–PET and PCI, and to identify signs of consciousness in otherwise unresponsive patients. METHODS: We jointly applied the Coma Recovery Scale-Revised, FDG–PET and PCI to assess 24 patients with non-acute disorders of consciousness or locked-in syndrome (13 male; 19–54 years old; 12 traumatic; 9 unresponsive wakefulness syndrome, 11 minimally conscious state; 2 emergence from the minimally conscious state, and 2 locked-in syndrome). RESULTS: FDG–PET and PCI provided congruent results in 22 patients, regardless of their behavioural diagnosis. Notably, FDG–PET and PCI revealed preserved metabolic rates and high complexity levels in four patients who were behaviourally unresponsive. CONCLUSION: We propose that jointly measuring the metabolic activity and the electrophysiological complexity of cortical circuits is a useful complement to the diagnosis and stratification of patients with disorders of consciousness. Elsevier 2017-02-06 /pmc/articles/PMC5318348/ /pubmed/28239544 http://dx.doi.org/10.1016/j.nicl.2017.02.002 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Bodart, Olivier
Gosseries, Olivia
Wannez, Sarah
Thibaut, Aurore
Annen, Jitka
Boly, Melanie
Rosanova, Mario
Casali, Adenauer G.
Casarotto, Silvia
Tononi, Giulio
Massimini, Marcello
Laureys, Steven
Measures of metabolism and complexity in the brain of patients with disorders of consciousness
title Measures of metabolism and complexity in the brain of patients with disorders of consciousness
title_full Measures of metabolism and complexity in the brain of patients with disorders of consciousness
title_fullStr Measures of metabolism and complexity in the brain of patients with disorders of consciousness
title_full_unstemmed Measures of metabolism and complexity in the brain of patients with disorders of consciousness
title_short Measures of metabolism and complexity in the brain of patients with disorders of consciousness
title_sort measures of metabolism and complexity in the brain of patients with disorders of consciousness
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318348/
https://www.ncbi.nlm.nih.gov/pubmed/28239544
http://dx.doi.org/10.1016/j.nicl.2017.02.002
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