Cargando…
Neuromuscular Diseases Affect Number Representation and Processing: An Exploratory Study
Spinal muscular atrophy (SMA) and Duchenne muscular dystrophy (DMD) both are rare genetic neuromuscular diseases with progressive loss of motor ability. The neuromotor developmental course of those diseases is well documented. In contrast, there is only little evidence about characteristics of gener...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450493/ https://www.ncbi.nlm.nih.gov/pubmed/34552528 http://dx.doi.org/10.3389/fpsyg.2021.697881 |
_version_ | 1784569656942526464 |
---|---|
author | Schmidt, Hendrikje Felisatti, Arianna von Aster, Michael Wilbert, Jürgen von Moers, Arpad Fischer, Martin H. |
author_facet | Schmidt, Hendrikje Felisatti, Arianna von Aster, Michael Wilbert, Jürgen von Moers, Arpad Fischer, Martin H. |
author_sort | Schmidt, Hendrikje |
collection | PubMed |
description | Spinal muscular atrophy (SMA) and Duchenne muscular dystrophy (DMD) both are rare genetic neuromuscular diseases with progressive loss of motor ability. The neuromotor developmental course of those diseases is well documented. In contrast, there is only little evidence about characteristics of general and specific cognitive development. In both conditions the final motor outcome is characterized by an inability to move autonomously: children with SMA never accomplish independent motoric exploration of their environment, while children with DMD do but later lose this ability again. These profound differences in developmental pathways might affect cognitive development of SMA vs. DMD children, as cognition is shaped by individual motor experiences. DMD patients show impaired executive functions, working memory, and verbal IQ, whereas only motor ability seems to be impaired in SMA. Advanced cognitive capacity in SMA may serve as a compensatory mechanism for achieving in education, career progression, and social satisfaction. This study aimed to relate differences in basic numerical concepts and arithmetic achievement in SMA and DMD patients to differences in their motor development and resulting sensorimotor and environmental experiences. Horizontal and vertical spatial-numerical associations were explored in SMA/DMD children ranging between 6 and 12 years through the random number generation task. Furthermore, arithmetic skills as well as general cognitive ability were assessed. Groups differed in spatial number processing as well as in arithmetic and domain-general cognitive functions. Children with SMA showed no horizontal and even reversed vertical spatial-numerical associations. Children with DMD on the other hand revealed patterns in spatial numerical associations comparable to healthy developing children. From the embodied Cognition perspective, early sensorimotor experience does play a role in development of mental number representations. However, it remains open whether and how this becomes relevant for the acquisition of higher order cognitive and arithmetic skills. |
format | Online Article Text |
id | pubmed-8450493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84504932021-09-21 Neuromuscular Diseases Affect Number Representation and Processing: An Exploratory Study Schmidt, Hendrikje Felisatti, Arianna von Aster, Michael Wilbert, Jürgen von Moers, Arpad Fischer, Martin H. Front Psychol Psychology Spinal muscular atrophy (SMA) and Duchenne muscular dystrophy (DMD) both are rare genetic neuromuscular diseases with progressive loss of motor ability. The neuromotor developmental course of those diseases is well documented. In contrast, there is only little evidence about characteristics of general and specific cognitive development. In both conditions the final motor outcome is characterized by an inability to move autonomously: children with SMA never accomplish independent motoric exploration of their environment, while children with DMD do but later lose this ability again. These profound differences in developmental pathways might affect cognitive development of SMA vs. DMD children, as cognition is shaped by individual motor experiences. DMD patients show impaired executive functions, working memory, and verbal IQ, whereas only motor ability seems to be impaired in SMA. Advanced cognitive capacity in SMA may serve as a compensatory mechanism for achieving in education, career progression, and social satisfaction. This study aimed to relate differences in basic numerical concepts and arithmetic achievement in SMA and DMD patients to differences in their motor development and resulting sensorimotor and environmental experiences. Horizontal and vertical spatial-numerical associations were explored in SMA/DMD children ranging between 6 and 12 years through the random number generation task. Furthermore, arithmetic skills as well as general cognitive ability were assessed. Groups differed in spatial number processing as well as in arithmetic and domain-general cognitive functions. Children with SMA showed no horizontal and even reversed vertical spatial-numerical associations. Children with DMD on the other hand revealed patterns in spatial numerical associations comparable to healthy developing children. From the embodied Cognition perspective, early sensorimotor experience does play a role in development of mental number representations. However, it remains open whether and how this becomes relevant for the acquisition of higher order cognitive and arithmetic skills. Frontiers Media S.A. 2021-09-06 /pmc/articles/PMC8450493/ /pubmed/34552528 http://dx.doi.org/10.3389/fpsyg.2021.697881 Text en Copyright © 2021 Schmidt, Felisatti, von Aster, Wilbert, von Moers and Fischer. https://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 | Psychology Schmidt, Hendrikje Felisatti, Arianna von Aster, Michael Wilbert, Jürgen von Moers, Arpad Fischer, Martin H. Neuromuscular Diseases Affect Number Representation and Processing: An Exploratory Study |
title | Neuromuscular Diseases Affect Number Representation and Processing: An Exploratory Study |
title_full | Neuromuscular Diseases Affect Number Representation and Processing: An Exploratory Study |
title_fullStr | Neuromuscular Diseases Affect Number Representation and Processing: An Exploratory Study |
title_full_unstemmed | Neuromuscular Diseases Affect Number Representation and Processing: An Exploratory Study |
title_short | Neuromuscular Diseases Affect Number Representation and Processing: An Exploratory Study |
title_sort | neuromuscular diseases affect number representation and processing: an exploratory study |
topic | Psychology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450493/ https://www.ncbi.nlm.nih.gov/pubmed/34552528 http://dx.doi.org/10.3389/fpsyg.2021.697881 |
work_keys_str_mv | AT schmidthendrikje neuromusculardiseasesaffectnumberrepresentationandprocessinganexploratorystudy AT felisattiarianna neuromusculardiseasesaffectnumberrepresentationandprocessinganexploratorystudy AT vonastermichael neuromusculardiseasesaffectnumberrepresentationandprocessinganexploratorystudy AT wilbertjurgen neuromusculardiseasesaffectnumberrepresentationandprocessinganexploratorystudy AT vonmoersarpad neuromusculardiseasesaffectnumberrepresentationandprocessinganexploratorystudy AT fischermartinh neuromusculardiseasesaffectnumberrepresentationandprocessinganexploratorystudy |