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Speech–Brain Frequency Entrainment of Dyslexia with and without Phonological Deficits
Developmental dyslexia is a cognitive disorder characterized by difficulties in linguistic processing. Our purpose is to distinguish subtypes of developmental dyslexia by the level of speech–EEG frequency entrainment (δ: 1–4; β: 12.5–22.5; γ1: 25–35; and γ2: 35–80 Hz) in word/pseudoword auditory dis...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760068/ https://www.ncbi.nlm.nih.gov/pubmed/33260681 http://dx.doi.org/10.3390/brainsci10120920 |
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author | Dushanova, Juliana Lalova, Yordanka Kalonkina, Antoaneta Tsokov, Stefan |
author_facet | Dushanova, Juliana Lalova, Yordanka Kalonkina, Antoaneta Tsokov, Stefan |
author_sort | Dushanova, Juliana |
collection | PubMed |
description | Developmental dyslexia is a cognitive disorder characterized by difficulties in linguistic processing. Our purpose is to distinguish subtypes of developmental dyslexia by the level of speech–EEG frequency entrainment (δ: 1–4; β: 12.5–22.5; γ1: 25–35; and γ2: 35–80 Hz) in word/pseudoword auditory discrimination. Depending on the type of disabilities, dyslexics can divide into two subtypes—with less pronounced phonological deficits (NoPhoDys—visual dyslexia) and with more pronounced ones (PhoDys—phonological dyslexia). For correctly recognized stimuli, the δ-entrainment is significantly worse in dyslexic children compared to controls at a level of speech prosody and syllabic analysis. Controls and NoPhoDys show a stronger δ-entrainment in the left-hemispheric auditory cortex (AC), anterior temporal lobe (ATL), frontal, and motor cortices than PhoDys. Dyslexic subgroups concerning normolexics have a deficit of δ-entrainment in the left ATL, inferior frontal gyrus (IFG), and the right AC. PhoDys has higher δ-entrainment in the posterior part of adjacent STS regions than NoPhoDys. Insufficient low-frequency β changes over the IFG, the inferior parietal lobe of PhoDys compared to NoPhoDys correspond to their worse phonological short-term memory. Left-dominant 30 Hz-entrainment for normolexics to phonemic frequencies characterizes the right AC, adjacent regions to superior temporal sulcus of dyslexics. The pronounced 40 Hz-entrainment in PhoDys than the other groups suggest a hearing “reassembly” and a poor phonological working memory. Shifting up to higher-frequency γ-entrainment in the AC of NoPhoDys can lead to verbal memory deficits. Different patterns of cortical reorganization based on the left or right hemisphere lead to differential dyslexic profiles. |
format | Online Article Text |
id | pubmed-7760068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77600682020-12-26 Speech–Brain Frequency Entrainment of Dyslexia with and without Phonological Deficits Dushanova, Juliana Lalova, Yordanka Kalonkina, Antoaneta Tsokov, Stefan Brain Sci Article Developmental dyslexia is a cognitive disorder characterized by difficulties in linguistic processing. Our purpose is to distinguish subtypes of developmental dyslexia by the level of speech–EEG frequency entrainment (δ: 1–4; β: 12.5–22.5; γ1: 25–35; and γ2: 35–80 Hz) in word/pseudoword auditory discrimination. Depending on the type of disabilities, dyslexics can divide into two subtypes—with less pronounced phonological deficits (NoPhoDys—visual dyslexia) and with more pronounced ones (PhoDys—phonological dyslexia). For correctly recognized stimuli, the δ-entrainment is significantly worse in dyslexic children compared to controls at a level of speech prosody and syllabic analysis. Controls and NoPhoDys show a stronger δ-entrainment in the left-hemispheric auditory cortex (AC), anterior temporal lobe (ATL), frontal, and motor cortices than PhoDys. Dyslexic subgroups concerning normolexics have a deficit of δ-entrainment in the left ATL, inferior frontal gyrus (IFG), and the right AC. PhoDys has higher δ-entrainment in the posterior part of adjacent STS regions than NoPhoDys. Insufficient low-frequency β changes over the IFG, the inferior parietal lobe of PhoDys compared to NoPhoDys correspond to their worse phonological short-term memory. Left-dominant 30 Hz-entrainment for normolexics to phonemic frequencies characterizes the right AC, adjacent regions to superior temporal sulcus of dyslexics. The pronounced 40 Hz-entrainment in PhoDys than the other groups suggest a hearing “reassembly” and a poor phonological working memory. Shifting up to higher-frequency γ-entrainment in the AC of NoPhoDys can lead to verbal memory deficits. Different patterns of cortical reorganization based on the left or right hemisphere lead to differential dyslexic profiles. MDPI 2020-11-28 /pmc/articles/PMC7760068/ /pubmed/33260681 http://dx.doi.org/10.3390/brainsci10120920 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Dushanova, Juliana Lalova, Yordanka Kalonkina, Antoaneta Tsokov, Stefan Speech–Brain Frequency Entrainment of Dyslexia with and without Phonological Deficits |
title | Speech–Brain Frequency Entrainment of Dyslexia with and without Phonological Deficits |
title_full | Speech–Brain Frequency Entrainment of Dyslexia with and without Phonological Deficits |
title_fullStr | Speech–Brain Frequency Entrainment of Dyslexia with and without Phonological Deficits |
title_full_unstemmed | Speech–Brain Frequency Entrainment of Dyslexia with and without Phonological Deficits |
title_short | Speech–Brain Frequency Entrainment of Dyslexia with and without Phonological Deficits |
title_sort | speech–brain frequency entrainment of dyslexia with and without phonological deficits |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760068/ https://www.ncbi.nlm.nih.gov/pubmed/33260681 http://dx.doi.org/10.3390/brainsci10120920 |
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