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ERPs Reveal the Time-Course of Aberrant Visual-Phonological Binding in Developmental Dyslexia

New evidence is accumulating for a deficit in binding visual-orthographic information with the corresponding phonological code in developmental dyslexia. Here, we identify the mechanisms underpinning this deficit using event-related brain potentials (ERPs) in dyslexic and control adult readers perfo...

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Autores principales: Jones, Manon W., Kuipers, Jan-Rouke, Thierry, Guillaume
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772455/
https://www.ncbi.nlm.nih.gov/pubmed/26973493
http://dx.doi.org/10.3389/fnhum.2016.00071
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author Jones, Manon W.
Kuipers, Jan-Rouke
Thierry, Guillaume
author_facet Jones, Manon W.
Kuipers, Jan-Rouke
Thierry, Guillaume
author_sort Jones, Manon W.
collection PubMed
description New evidence is accumulating for a deficit in binding visual-orthographic information with the corresponding phonological code in developmental dyslexia. Here, we identify the mechanisms underpinning this deficit using event-related brain potentials (ERPs) in dyslexic and control adult readers performing a letter-matching task. In each trial, a printed letter was presented synchronously with an auditory letter name. Incongruent (mismatched), frequent trials were interleaved with congruent (matched) infrequent target pairs, which participants were asked to report by pressing a button. In critical trials, incongruent letter pairs were mismatched but confusable in terms of their visual or phonological features. Typical readers showed early detection of deviant trials, indicated by larger modulation in the range of the phonological mismatch negativity (PMN) compared with standard trials. This was followed by stronger modulation of the P3b wave for visually confusable deviants and an increased lateralized readiness potential (LRP) for phonological deviants, compared with standards. In contrast, dyslexic readers showed reduced sensitivity to deviancy in the PMN range. Responses to deviants in the P3b range indicated normal letter recognition processes, but the LRP calculation revealed a specific impairment for visual-orthographic information during response selection in dyslexia. In a follow-up experiment using an analogous non-lexical task in the same participants, we found no reading-group differences, indicating a degree of specificity to over-learnt visual-phonological binding. Our findings indicate early insensitivity to visual-phonological binding in developmental dyslexia, coupled with difficulty selecting the correct orthographic code.
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spelling pubmed-47724552016-03-11 ERPs Reveal the Time-Course of Aberrant Visual-Phonological Binding in Developmental Dyslexia Jones, Manon W. Kuipers, Jan-Rouke Thierry, Guillaume Front Hum Neurosci Neuroscience New evidence is accumulating for a deficit in binding visual-orthographic information with the corresponding phonological code in developmental dyslexia. Here, we identify the mechanisms underpinning this deficit using event-related brain potentials (ERPs) in dyslexic and control adult readers performing a letter-matching task. In each trial, a printed letter was presented synchronously with an auditory letter name. Incongruent (mismatched), frequent trials were interleaved with congruent (matched) infrequent target pairs, which participants were asked to report by pressing a button. In critical trials, incongruent letter pairs were mismatched but confusable in terms of their visual or phonological features. Typical readers showed early detection of deviant trials, indicated by larger modulation in the range of the phonological mismatch negativity (PMN) compared with standard trials. This was followed by stronger modulation of the P3b wave for visually confusable deviants and an increased lateralized readiness potential (LRP) for phonological deviants, compared with standards. In contrast, dyslexic readers showed reduced sensitivity to deviancy in the PMN range. Responses to deviants in the P3b range indicated normal letter recognition processes, but the LRP calculation revealed a specific impairment for visual-orthographic information during response selection in dyslexia. In a follow-up experiment using an analogous non-lexical task in the same participants, we found no reading-group differences, indicating a degree of specificity to over-learnt visual-phonological binding. Our findings indicate early insensitivity to visual-phonological binding in developmental dyslexia, coupled with difficulty selecting the correct orthographic code. Frontiers Media S.A. 2016-03-01 /pmc/articles/PMC4772455/ /pubmed/26973493 http://dx.doi.org/10.3389/fnhum.2016.00071 Text en Copyright © 2016 Jones, Kuipers and Thierry. 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
Jones, Manon W.
Kuipers, Jan-Rouke
Thierry, Guillaume
ERPs Reveal the Time-Course of Aberrant Visual-Phonological Binding in Developmental Dyslexia
title ERPs Reveal the Time-Course of Aberrant Visual-Phonological Binding in Developmental Dyslexia
title_full ERPs Reveal the Time-Course of Aberrant Visual-Phonological Binding in Developmental Dyslexia
title_fullStr ERPs Reveal the Time-Course of Aberrant Visual-Phonological Binding in Developmental Dyslexia
title_full_unstemmed ERPs Reveal the Time-Course of Aberrant Visual-Phonological Binding in Developmental Dyslexia
title_short ERPs Reveal the Time-Course of Aberrant Visual-Phonological Binding in Developmental Dyslexia
title_sort erps reveal the time-course of aberrant visual-phonological binding in developmental dyslexia
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772455/
https://www.ncbi.nlm.nih.gov/pubmed/26973493
http://dx.doi.org/10.3389/fnhum.2016.00071
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