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Impaired cortical processing of inspiratory loads in children with chronic respiratory defects
BACKGROUND: Inspiratory occlusion evoked cortical potentials (the respiratory related-evoked potentials, RREPs) bear witness of the processing of changes in respiratory mechanics by the brain. Their impairment in children having suffered near-fatal asthma supports the hypothesis that relates asthma...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2020473/ https://www.ncbi.nlm.nih.gov/pubmed/17822538 http://dx.doi.org/10.1186/1465-9921-8-61 |
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author | Fauroux, Brigitte Renault, Francis Boelle, Pierre Yves Donzel-Raynaud, Christine Nicot, Frédéric Clément, Annick Straus, Christian Similowski, Thomas |
author_facet | Fauroux, Brigitte Renault, Francis Boelle, Pierre Yves Donzel-Raynaud, Christine Nicot, Frédéric Clément, Annick Straus, Christian Similowski, Thomas |
author_sort | Fauroux, Brigitte |
collection | PubMed |
description | BACKGROUND: Inspiratory occlusion evoked cortical potentials (the respiratory related-evoked potentials, RREPs) bear witness of the processing of changes in respiratory mechanics by the brain. Their impairment in children having suffered near-fatal asthma supports the hypothesis that relates asthma severity with the ability of the patients to perceive respiratory changes. It is not known whether or not chronic respiratory defects are associated with an alteration in brain processing of inspiratory loads. The aim of the present study was to compare the presence, the latencies and the amplitudes of the P1, N1, P2, and N2 components of the RREPs in children with chronic lung or neuromuscular disease. METHODS: RREPs were recorded in patients with stable asthma (n = 21), cystic fibrosis (n = 32), and neuromuscular disease (n = 16) and in healthy controls (n = 11). RESULTS: The 4 RREP components were significantly less frequently observed in the 3 groups of patients than in the controls. Within the patient groups, the N1 and the P2 components were significantly less frequently observed in the patients with asthma (16/21 for both components) and cystic fibrosis (20/32 and 14/32) than in the patients with neuromuscular disease (15/16 and 16/16). When present, the latencies and amplitudes of the 4 components were similar in the patients and controls. CONCLUSION: Chronic ventilatory defects in children are associated with an impaired cortical processing of afferent respiratory signals. |
format | Text |
id | pubmed-2020473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-20204732007-10-13 Impaired cortical processing of inspiratory loads in children with chronic respiratory defects Fauroux, Brigitte Renault, Francis Boelle, Pierre Yves Donzel-Raynaud, Christine Nicot, Frédéric Clément, Annick Straus, Christian Similowski, Thomas Respir Res Research BACKGROUND: Inspiratory occlusion evoked cortical potentials (the respiratory related-evoked potentials, RREPs) bear witness of the processing of changes in respiratory mechanics by the brain. Their impairment in children having suffered near-fatal asthma supports the hypothesis that relates asthma severity with the ability of the patients to perceive respiratory changes. It is not known whether or not chronic respiratory defects are associated with an alteration in brain processing of inspiratory loads. The aim of the present study was to compare the presence, the latencies and the amplitudes of the P1, N1, P2, and N2 components of the RREPs in children with chronic lung or neuromuscular disease. METHODS: RREPs were recorded in patients with stable asthma (n = 21), cystic fibrosis (n = 32), and neuromuscular disease (n = 16) and in healthy controls (n = 11). RESULTS: The 4 RREP components were significantly less frequently observed in the 3 groups of patients than in the controls. Within the patient groups, the N1 and the P2 components were significantly less frequently observed in the patients with asthma (16/21 for both components) and cystic fibrosis (20/32 and 14/32) than in the patients with neuromuscular disease (15/16 and 16/16). When present, the latencies and amplitudes of the 4 components were similar in the patients and controls. CONCLUSION: Chronic ventilatory defects in children are associated with an impaired cortical processing of afferent respiratory signals. BioMed Central 2007 2007-09-06 /pmc/articles/PMC2020473/ /pubmed/17822538 http://dx.doi.org/10.1186/1465-9921-8-61 Text en Copyright © 2007 Fauroux et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Fauroux, Brigitte Renault, Francis Boelle, Pierre Yves Donzel-Raynaud, Christine Nicot, Frédéric Clément, Annick Straus, Christian Similowski, Thomas Impaired cortical processing of inspiratory loads in children with chronic respiratory defects |
title | Impaired cortical processing of inspiratory loads in children with chronic respiratory defects |
title_full | Impaired cortical processing of inspiratory loads in children with chronic respiratory defects |
title_fullStr | Impaired cortical processing of inspiratory loads in children with chronic respiratory defects |
title_full_unstemmed | Impaired cortical processing of inspiratory loads in children with chronic respiratory defects |
title_short | Impaired cortical processing of inspiratory loads in children with chronic respiratory defects |
title_sort | impaired cortical processing of inspiratory loads in children with chronic respiratory defects |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2020473/ https://www.ncbi.nlm.nih.gov/pubmed/17822538 http://dx.doi.org/10.1186/1465-9921-8-61 |
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