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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
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.
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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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