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Primary lateral sclerosis: consensus diagnostic criteria
Primary lateral sclerosis (PLS) is a neurodegenerative disorder of the adult motor system. Characterised by a slowly progressive upper motor neuron syndrome, the diagnosis is clinical, after exclusion of structural, neurodegenerative and metabolic mimics. Differentiation of PLS from upper motor neur...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147236/ https://www.ncbi.nlm.nih.gov/pubmed/32029539 http://dx.doi.org/10.1136/jnnp-2019-322541 |
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author | Turner, Martin R Barohn, Richard J Corcia, Philippe Fink, John K Harms, Matthew B Kiernan, Matthew C Ravits, John Silani, Vincenzo Simmons, Zachary Statland, Jeffrey van den Berg, Leonard H Mitsumoto, Hiroshi |
author_facet | Turner, Martin R Barohn, Richard J Corcia, Philippe Fink, John K Harms, Matthew B Kiernan, Matthew C Ravits, John Silani, Vincenzo Simmons, Zachary Statland, Jeffrey van den Berg, Leonard H Mitsumoto, Hiroshi |
author_sort | Turner, Martin R |
collection | PubMed |
description | Primary lateral sclerosis (PLS) is a neurodegenerative disorder of the adult motor system. Characterised by a slowly progressive upper motor neuron syndrome, the diagnosis is clinical, after exclusion of structural, neurodegenerative and metabolic mimics. Differentiation of PLS from upper motor neuron-predominant forms of amyotrophic lateral sclerosis remains a significant challenge in the early symptomatic phase of both disorders, with ongoing debate as to whether they form a clinical and histopathological continuum. Current diagnostic criteria for PLS may be a barrier to therapeutic development, requiring long delays between symptom onset and formal diagnosis. While new technologies sensitive to both upper and lower motor neuron involvement may ultimately resolve controversies in the diagnosis of PLS, we present updated consensus diagnostic criteria with the aim of reducing diagnostic delay, optimising therapeutic trial design and catalysing the development of disease-modifying therapy. |
format | Online Article Text |
id | pubmed-7147236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-71472362020-04-15 Primary lateral sclerosis: consensus diagnostic criteria Turner, Martin R Barohn, Richard J Corcia, Philippe Fink, John K Harms, Matthew B Kiernan, Matthew C Ravits, John Silani, Vincenzo Simmons, Zachary Statland, Jeffrey van den Berg, Leonard H Mitsumoto, Hiroshi J Neurol Neurosurg Psychiatry Neurodegeneration Primary lateral sclerosis (PLS) is a neurodegenerative disorder of the adult motor system. Characterised by a slowly progressive upper motor neuron syndrome, the diagnosis is clinical, after exclusion of structural, neurodegenerative and metabolic mimics. Differentiation of PLS from upper motor neuron-predominant forms of amyotrophic lateral sclerosis remains a significant challenge in the early symptomatic phase of both disorders, with ongoing debate as to whether they form a clinical and histopathological continuum. Current diagnostic criteria for PLS may be a barrier to therapeutic development, requiring long delays between symptom onset and formal diagnosis. While new technologies sensitive to both upper and lower motor neuron involvement may ultimately resolve controversies in the diagnosis of PLS, we present updated consensus diagnostic criteria with the aim of reducing diagnostic delay, optimising therapeutic trial design and catalysing the development of disease-modifying therapy. BMJ Publishing Group 2020-04 2020-02-06 /pmc/articles/PMC7147236/ /pubmed/32029539 http://dx.doi.org/10.1136/jnnp-2019-322541 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Neurodegeneration Turner, Martin R Barohn, Richard J Corcia, Philippe Fink, John K Harms, Matthew B Kiernan, Matthew C Ravits, John Silani, Vincenzo Simmons, Zachary Statland, Jeffrey van den Berg, Leonard H Mitsumoto, Hiroshi Primary lateral sclerosis: consensus diagnostic criteria |
title | Primary lateral sclerosis: consensus diagnostic criteria |
title_full | Primary lateral sclerosis: consensus diagnostic criteria |
title_fullStr | Primary lateral sclerosis: consensus diagnostic criteria |
title_full_unstemmed | Primary lateral sclerosis: consensus diagnostic criteria |
title_short | Primary lateral sclerosis: consensus diagnostic criteria |
title_sort | primary lateral sclerosis: consensus diagnostic criteria |
topic | Neurodegeneration |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147236/ https://www.ncbi.nlm.nih.gov/pubmed/32029539 http://dx.doi.org/10.1136/jnnp-2019-322541 |
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