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Cognitive impairment in neuromuscular diseases: A systematic review
Neuromuscular diseases are multifactorial pathologies characterized by extensive muscle fiber damage that leads to the activation of satellite cells and to the exhaustion of their pool, with consequent impairment of neurobiological aspects, such as cognition and motor control. To review the knowledg...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications, Pavia, Italy
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050451/ https://www.ncbi.nlm.nih.gov/pubmed/30069288 http://dx.doi.org/10.4081/ni.2018.7473 |
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author | Orsini, Marco Carolina, Ana Ferreira, Andorinho de F. de Assis, Anna Carolina Damm Magalhães, Thais Teixeira, Silmar Bastos, Victor Hugo Marinho, Victor Oliveira, Thomaz Fiorelli, Rossano Oliveira, Acary Bulle de Freitas, Marcos R.G. |
author_facet | Orsini, Marco Carolina, Ana Ferreira, Andorinho de F. de Assis, Anna Carolina Damm Magalhães, Thais Teixeira, Silmar Bastos, Victor Hugo Marinho, Victor Oliveira, Thomaz Fiorelli, Rossano Oliveira, Acary Bulle de Freitas, Marcos R.G. |
author_sort | Orsini, Marco |
collection | PubMed |
description | Neuromuscular diseases are multifactorial pathologies characterized by extensive muscle fiber damage that leads to the activation of satellite cells and to the exhaustion of their pool, with consequent impairment of neurobiological aspects, such as cognition and motor control. To review the knowledge and obtain a broad view of the cognitive impairment on Neuromuscular Diseases. Cognitive impairment in neuromuscular disease was explored; a literature search up to October 2017 was conducted, including experimental studies, case reports and reviews written in English. Keywords included Cognitive Impairment, Neuromuscular Diseases, Motor Neuron Diseases, Dystrophinopathies and Mitochondrial Disorders. Several cognitive evaluation scales, neuroimaging scans, genetic analysis and laboratory applications in neuromuscular diseases, especially when it comes to the Motor Neuron Diseases, Dystrophinopathies and Mitochondrial Disorders. In addition, organisms model using rats in the genetic analysis and laboratory applications to verify the cognitive and neuromuscular impacts. Several studies indicate that congenital molecular alterations in neuromuscular diseases promote cognitive dysfunctions. Understanding these mechanisms may in the future guide the proper management of the patient, evaluation, establishment of prognosis, choice of treatment and development of innovative interventions such as gene therapy. |
format | Online Article Text |
id | pubmed-6050451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | PAGEPress Publications, Pavia, Italy |
record_format | MEDLINE/PubMed |
spelling | pubmed-60504512018-08-01 Cognitive impairment in neuromuscular diseases: A systematic review Orsini, Marco Carolina, Ana Ferreira, Andorinho de F. de Assis, Anna Carolina Damm Magalhães, Thais Teixeira, Silmar Bastos, Victor Hugo Marinho, Victor Oliveira, Thomaz Fiorelli, Rossano Oliveira, Acary Bulle de Freitas, Marcos R.G. Neurol Int Review Neuromuscular diseases are multifactorial pathologies characterized by extensive muscle fiber damage that leads to the activation of satellite cells and to the exhaustion of their pool, with consequent impairment of neurobiological aspects, such as cognition and motor control. To review the knowledge and obtain a broad view of the cognitive impairment on Neuromuscular Diseases. Cognitive impairment in neuromuscular disease was explored; a literature search up to October 2017 was conducted, including experimental studies, case reports and reviews written in English. Keywords included Cognitive Impairment, Neuromuscular Diseases, Motor Neuron Diseases, Dystrophinopathies and Mitochondrial Disorders. Several cognitive evaluation scales, neuroimaging scans, genetic analysis and laboratory applications in neuromuscular diseases, especially when it comes to the Motor Neuron Diseases, Dystrophinopathies and Mitochondrial Disorders. In addition, organisms model using rats in the genetic analysis and laboratory applications to verify the cognitive and neuromuscular impacts. Several studies indicate that congenital molecular alterations in neuromuscular diseases promote cognitive dysfunctions. Understanding these mechanisms may in the future guide the proper management of the patient, evaluation, establishment of prognosis, choice of treatment and development of innovative interventions such as gene therapy. PAGEPress Publications, Pavia, Italy 2018-07-04 /pmc/articles/PMC6050451/ /pubmed/30069288 http://dx.doi.org/10.4081/ni.2018.7473 Text en ©Copyright M. Orsini et al., 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Review Orsini, Marco Carolina, Ana Ferreira, Andorinho de F. de Assis, Anna Carolina Damm Magalhães, Thais Teixeira, Silmar Bastos, Victor Hugo Marinho, Victor Oliveira, Thomaz Fiorelli, Rossano Oliveira, Acary Bulle de Freitas, Marcos R.G. Cognitive impairment in neuromuscular diseases: A systematic review |
title | Cognitive impairment in neuromuscular diseases: A systematic review |
title_full | Cognitive impairment in neuromuscular diseases: A systematic review |
title_fullStr | Cognitive impairment in neuromuscular diseases: A systematic review |
title_full_unstemmed | Cognitive impairment in neuromuscular diseases: A systematic review |
title_short | Cognitive impairment in neuromuscular diseases: A systematic review |
title_sort | cognitive impairment in neuromuscular diseases: a systematic review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050451/ https://www.ncbi.nlm.nih.gov/pubmed/30069288 http://dx.doi.org/10.4081/ni.2018.7473 |
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