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Linking Early Life Hypothalamic–Pituitary–Adrenal Axis Functioning, Brain Asymmetries, and Personality Traits in Dyslexia: An Informative Case Study

Developmental dyslexia (DD) is a multi-system disorder, combining influences of susceptibility genes and environmental factors. The causative interaction between specific genetic factors, brain regions, and personality/mental disorders, as well as specific learning disabilities, has been thoroughly...

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Autores principales: Zakopoulou, Victoria, Vlaikou, Angeliki-Maria, Darsinou, Marousa, Papadopoulou, Zoe, Theodoridou, Daniela, Papageorgiou, Kyriaki, Alexiou, George A., Bougias, Haralambos, Siafaka, Vassiliki, Zoccolotti, Pierluigi, Chroussos, George P., Syrrou, Maria, Michaelidis, Theologos M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779713/
https://www.ncbi.nlm.nih.gov/pubmed/31632253
http://dx.doi.org/10.3389/fnhum.2019.00327
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author Zakopoulou, Victoria
Vlaikou, Angeliki-Maria
Darsinou, Marousa
Papadopoulou, Zoe
Theodoridou, Daniela
Papageorgiou, Kyriaki
Alexiou, George A.
Bougias, Haralambos
Siafaka, Vassiliki
Zoccolotti, Pierluigi
Chroussos, George P.
Syrrou, Maria
Michaelidis, Theologos M.
author_facet Zakopoulou, Victoria
Vlaikou, Angeliki-Maria
Darsinou, Marousa
Papadopoulou, Zoe
Theodoridou, Daniela
Papageorgiou, Kyriaki
Alexiou, George A.
Bougias, Haralambos
Siafaka, Vassiliki
Zoccolotti, Pierluigi
Chroussos, George P.
Syrrou, Maria
Michaelidis, Theologos M.
author_sort Zakopoulou, Victoria
collection PubMed
description Developmental dyslexia (DD) is a multi-system disorder, combining influences of susceptibility genes and environmental factors. The causative interaction between specific genetic factors, brain regions, and personality/mental disorders, as well as specific learning disabilities, has been thoroughly investigated with regard to the approach of developing a multifaceted diagnostic procedure with an intervention strategy potential. In an attempt to add new translational evidence to the interconnection of the above factors in the occurrence of DD, we performed a combinatorial analysis of brain asymmetries, personality traits, cognitive and learning skills, and expression profiles of selected genes in an adult, early diagnosed with DD, and in his son of typical development. We focused on the expression of genes, based on the assumption that the regulation of transcription may be affected by genetic and epigenetic factors. The results highlighted a potential chain link between neuroplasticity-related as well as stress-related genes, such as BDNF, Sox4, mineralocorticoid receptor (MR), and GILZ, leftward asymmetries in the amygdala and selective cerebellum lobules, and tendencies for personality disorders and dyslexia. This correlation may reflect the presence of a specific neuro-epigenetic component of DD, ensuing from the continuous, multifaceted difficulties in the acquisition of cognitive and learning skills, which in turn may act as a fostering mechanism for the onset of long-term disorders. This is in line with recent findings demonstrating a dysfunction in processes supported by rapid neural adaptation in children and adults with dyslexia. Accordingly, the co-evaluation of all the above parameters may indicate a stress-related dyslexia endophenotype that should be carefully considered for a more integrated diagnosis and effective intervention.
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spelling pubmed-67797132019-10-18 Linking Early Life Hypothalamic–Pituitary–Adrenal Axis Functioning, Brain Asymmetries, and Personality Traits in Dyslexia: An Informative Case Study Zakopoulou, Victoria Vlaikou, Angeliki-Maria Darsinou, Marousa Papadopoulou, Zoe Theodoridou, Daniela Papageorgiou, Kyriaki Alexiou, George A. Bougias, Haralambos Siafaka, Vassiliki Zoccolotti, Pierluigi Chroussos, George P. Syrrou, Maria Michaelidis, Theologos M. Front Hum Neurosci Human Neuroscience Developmental dyslexia (DD) is a multi-system disorder, combining influences of susceptibility genes and environmental factors. The causative interaction between specific genetic factors, brain regions, and personality/mental disorders, as well as specific learning disabilities, has been thoroughly investigated with regard to the approach of developing a multifaceted diagnostic procedure with an intervention strategy potential. In an attempt to add new translational evidence to the interconnection of the above factors in the occurrence of DD, we performed a combinatorial analysis of brain asymmetries, personality traits, cognitive and learning skills, and expression profiles of selected genes in an adult, early diagnosed with DD, and in his son of typical development. We focused on the expression of genes, based on the assumption that the regulation of transcription may be affected by genetic and epigenetic factors. The results highlighted a potential chain link between neuroplasticity-related as well as stress-related genes, such as BDNF, Sox4, mineralocorticoid receptor (MR), and GILZ, leftward asymmetries in the amygdala and selective cerebellum lobules, and tendencies for personality disorders and dyslexia. This correlation may reflect the presence of a specific neuro-epigenetic component of DD, ensuing from the continuous, multifaceted difficulties in the acquisition of cognitive and learning skills, which in turn may act as a fostering mechanism for the onset of long-term disorders. This is in line with recent findings demonstrating a dysfunction in processes supported by rapid neural adaptation in children and adults with dyslexia. Accordingly, the co-evaluation of all the above parameters may indicate a stress-related dyslexia endophenotype that should be carefully considered for a more integrated diagnosis and effective intervention. Frontiers Media S.A. 2019-10-01 /pmc/articles/PMC6779713/ /pubmed/31632253 http://dx.doi.org/10.3389/fnhum.2019.00327 Text en Copyright © 2019 Zakopoulou, Vlaikou, Darsinou, Papadopoulou, Theodoridou, Papageorgiou, Alexiou, Bougias, Siafaka, Zoccolotti, Chroussos, Syrrou and Michaelidis. 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 or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) 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 Human Neuroscience
Zakopoulou, Victoria
Vlaikou, Angeliki-Maria
Darsinou, Marousa
Papadopoulou, Zoe
Theodoridou, Daniela
Papageorgiou, Kyriaki
Alexiou, George A.
Bougias, Haralambos
Siafaka, Vassiliki
Zoccolotti, Pierluigi
Chroussos, George P.
Syrrou, Maria
Michaelidis, Theologos M.
Linking Early Life Hypothalamic–Pituitary–Adrenal Axis Functioning, Brain Asymmetries, and Personality Traits in Dyslexia: An Informative Case Study
title Linking Early Life Hypothalamic–Pituitary–Adrenal Axis Functioning, Brain Asymmetries, and Personality Traits in Dyslexia: An Informative Case Study
title_full Linking Early Life Hypothalamic–Pituitary–Adrenal Axis Functioning, Brain Asymmetries, and Personality Traits in Dyslexia: An Informative Case Study
title_fullStr Linking Early Life Hypothalamic–Pituitary–Adrenal Axis Functioning, Brain Asymmetries, and Personality Traits in Dyslexia: An Informative Case Study
title_full_unstemmed Linking Early Life Hypothalamic–Pituitary–Adrenal Axis Functioning, Brain Asymmetries, and Personality Traits in Dyslexia: An Informative Case Study
title_short Linking Early Life Hypothalamic–Pituitary–Adrenal Axis Functioning, Brain Asymmetries, and Personality Traits in Dyslexia: An Informative Case Study
title_sort linking early life hypothalamic–pituitary–adrenal axis functioning, brain asymmetries, and personality traits in dyslexia: an informative case study
topic Human Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779713/
https://www.ncbi.nlm.nih.gov/pubmed/31632253
http://dx.doi.org/10.3389/fnhum.2019.00327
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