Cargando…
Deciphering Multiple Sclerosis Progression
Multiple sclerosis (MS) is primarily an inflammatory and degenerative disease of the central nervous system, triggered by unknown environmental factors in patients with predisposing genetic risk profiles. The prevention of neurological disability is one of the essential goals to be achieved in a pat...
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/PMC8058428/ https://www.ncbi.nlm.nih.gov/pubmed/33897583 http://dx.doi.org/10.3389/fneur.2021.608491 |
_version_ | 1783681013438742528 |
---|---|
author | Meca-Lallana, Virginia Berenguer-Ruiz, Leticia Carreres-Polo, Joan Eichau-Madueño, Sara Ferrer-Lozano, Jaime Forero, Lucía Higueras, Yolanda Téllez Lara, Nieves Vidal-Jordana, Angela Pérez-Miralles, Francisco Carlos |
author_facet | Meca-Lallana, Virginia Berenguer-Ruiz, Leticia Carreres-Polo, Joan Eichau-Madueño, Sara Ferrer-Lozano, Jaime Forero, Lucía Higueras, Yolanda Téllez Lara, Nieves Vidal-Jordana, Angela Pérez-Miralles, Francisco Carlos |
author_sort | Meca-Lallana, Virginia |
collection | PubMed |
description | Multiple sclerosis (MS) is primarily an inflammatory and degenerative disease of the central nervous system, triggered by unknown environmental factors in patients with predisposing genetic risk profiles. The prevention of neurological disability is one of the essential goals to be achieved in a patient with MS. However, the pathogenic mechanisms driving the progressive phase of the disease remain unknown. It was described that the pathophysiological mechanisms associated with disease progression are present from disease onset. In daily practice, there is a lack of clinical, radiological, or biological markers that favor an early detection of the disease's progression. Different definitions of disability progression were used in clinical trials. According to the most descriptive, progression was defined as a minimum increase in the Expanded Disability Status Scale (EDSS) of 1.5, 1.0, or 0.5 from a baseline level of 0, 1.0–5.0, and 5.5, respectively. Nevertheless, the EDSS is not the most sensitive scale to assess progression, and there is no consensus regarding any specific diagnostic criteria for disability progression. This review document discusses the current pathophysiological concepts associated with MS progression, the different measurement strategies, the biomarkers associated with disability progression, and the available pharmacologic therapeutic approaches. |
format | Online Article Text |
id | pubmed-8058428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80584282021-04-22 Deciphering Multiple Sclerosis Progression Meca-Lallana, Virginia Berenguer-Ruiz, Leticia Carreres-Polo, Joan Eichau-Madueño, Sara Ferrer-Lozano, Jaime Forero, Lucía Higueras, Yolanda Téllez Lara, Nieves Vidal-Jordana, Angela Pérez-Miralles, Francisco Carlos Front Neurol Neurology Multiple sclerosis (MS) is primarily an inflammatory and degenerative disease of the central nervous system, triggered by unknown environmental factors in patients with predisposing genetic risk profiles. The prevention of neurological disability is one of the essential goals to be achieved in a patient with MS. However, the pathogenic mechanisms driving the progressive phase of the disease remain unknown. It was described that the pathophysiological mechanisms associated with disease progression are present from disease onset. In daily practice, there is a lack of clinical, radiological, or biological markers that favor an early detection of the disease's progression. Different definitions of disability progression were used in clinical trials. According to the most descriptive, progression was defined as a minimum increase in the Expanded Disability Status Scale (EDSS) of 1.5, 1.0, or 0.5 from a baseline level of 0, 1.0–5.0, and 5.5, respectively. Nevertheless, the EDSS is not the most sensitive scale to assess progression, and there is no consensus regarding any specific diagnostic criteria for disability progression. This review document discusses the current pathophysiological concepts associated with MS progression, the different measurement strategies, the biomarkers associated with disability progression, and the available pharmacologic therapeutic approaches. Frontiers Media S.A. 2021-04-07 /pmc/articles/PMC8058428/ /pubmed/33897583 http://dx.doi.org/10.3389/fneur.2021.608491 Text en Copyright © 2021 Meca-Lallana, Berenguer-Ruiz, Carreres-Polo, Eichau-Madueño, Ferrer-Lozano, Forero, Higueras, Téllez Lara, Vidal-Jordana and Pérez-Miralles. 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 | Neurology Meca-Lallana, Virginia Berenguer-Ruiz, Leticia Carreres-Polo, Joan Eichau-Madueño, Sara Ferrer-Lozano, Jaime Forero, Lucía Higueras, Yolanda Téllez Lara, Nieves Vidal-Jordana, Angela Pérez-Miralles, Francisco Carlos Deciphering Multiple Sclerosis Progression |
title | Deciphering Multiple Sclerosis Progression |
title_full | Deciphering Multiple Sclerosis Progression |
title_fullStr | Deciphering Multiple Sclerosis Progression |
title_full_unstemmed | Deciphering Multiple Sclerosis Progression |
title_short | Deciphering Multiple Sclerosis Progression |
title_sort | deciphering multiple sclerosis progression |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8058428/ https://www.ncbi.nlm.nih.gov/pubmed/33897583 http://dx.doi.org/10.3389/fneur.2021.608491 |
work_keys_str_mv | AT mecalallanavirginia decipheringmultiplesclerosisprogression AT berenguerruizleticia decipheringmultiplesclerosisprogression AT carrerespolojoan decipheringmultiplesclerosisprogression AT eichaumaduenosara decipheringmultiplesclerosisprogression AT ferrerlozanojaime decipheringmultiplesclerosisprogression AT forerolucia decipheringmultiplesclerosisprogression AT higuerasyolanda decipheringmultiplesclerosisprogression AT tellezlaranieves decipheringmultiplesclerosisprogression AT vidaljordanaangela decipheringmultiplesclerosisprogression AT perezmirallesfranciscocarlos decipheringmultiplesclerosisprogression |