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A proposed staging system for amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis is a neurodegenerative disorder characterized by progressive loss of upper and lower motor neurons, with a median survival of 2–3 years. Although various phenotypic and research diagnostic classification systems exist and several prognostic models have been generated, t...

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Autores principales: Roche, Jose C., Rojas-Garcia, Ricardo, Scott, Kirsten M., Scotton, William, Ellis, Catherine E., Burman, Rachel, Wijesekera, Lokesh, Turner, Martin R., Leigh, P. Nigel, Shaw, Christopher E., Al-Chalabi, Ammar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3286327/
https://www.ncbi.nlm.nih.gov/pubmed/22271664
http://dx.doi.org/10.1093/brain/awr351
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author Roche, Jose C.
Rojas-Garcia, Ricardo
Scott, Kirsten M.
Scotton, William
Ellis, Catherine E.
Burman, Rachel
Wijesekera, Lokesh
Turner, Martin R.
Leigh, P. Nigel
Shaw, Christopher E.
Al-Chalabi, Ammar
author_facet Roche, Jose C.
Rojas-Garcia, Ricardo
Scott, Kirsten M.
Scotton, William
Ellis, Catherine E.
Burman, Rachel
Wijesekera, Lokesh
Turner, Martin R.
Leigh, P. Nigel
Shaw, Christopher E.
Al-Chalabi, Ammar
author_sort Roche, Jose C.
collection PubMed
description Amyotrophic lateral sclerosis is a neurodegenerative disorder characterized by progressive loss of upper and lower motor neurons, with a median survival of 2–3 years. Although various phenotypic and research diagnostic classification systems exist and several prognostic models have been generated, there is no staging system. Staging criteria for amyotrophic lateral sclerosis would help to provide a universal and objective measure of disease progression with benefits for patient care, resource allocation, research classifications and clinical trial design. We therefore sought to define easily identified clinical milestones that could be shown to occur at specific points in the disease course, reflect disease progression and impact prognosis and treatment. A tertiary referral centre clinical database was analysed, consisting of 1471 patients with amyotrophic lateral sclerosis seen between 1993 and 2007. Milestones were defined as symptom onset (functional involvement by weakness, wasting, spasticity, dysarthria or dysphagia of one central nervous system region defined as bulbar, upper limb, lower limb or diaphragmatic), diagnosis, functional involvement of a second region, functional involvement of a third region, needing gastrostomy and non-invasive ventilation. Milestone timings were standardized as proportions of time elapsed through the disease course using information from patients who had died by dividing time to a milestone by disease duration. Milestones occurred at predictable proportions of the disease course. Diagnosis occurred at 35% through the disease course, involvement of a second region at 38%, a third region at 61%, need for gastrostomy at 77% and need for non-invasive ventilation at 80%. We therefore propose a simple staging system for amyotrophic lateral sclerosis. Stage 1: symptom onset (involvement of first region); Stage 2A: diagnosis; Stage 2B: involvement of second region; Stage 3: involvement of third region; Stage 4A: need for gastrostomy; and Stage 4B: need for non-invasive ventilation. Validation of this staging system will require further studies in other populations, in population registers and in other clinic databases. The standardized times to milestones may well vary between different studies and populations, although the stages themselves and their meanings are likely to remain unchanged.
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spelling pubmed-32863272012-02-27 A proposed staging system for amyotrophic lateral sclerosis Roche, Jose C. Rojas-Garcia, Ricardo Scott, Kirsten M. Scotton, William Ellis, Catherine E. Burman, Rachel Wijesekera, Lokesh Turner, Martin R. Leigh, P. Nigel Shaw, Christopher E. Al-Chalabi, Ammar Brain Original Articles Amyotrophic lateral sclerosis is a neurodegenerative disorder characterized by progressive loss of upper and lower motor neurons, with a median survival of 2–3 years. Although various phenotypic and research diagnostic classification systems exist and several prognostic models have been generated, there is no staging system. Staging criteria for amyotrophic lateral sclerosis would help to provide a universal and objective measure of disease progression with benefits for patient care, resource allocation, research classifications and clinical trial design. We therefore sought to define easily identified clinical milestones that could be shown to occur at specific points in the disease course, reflect disease progression and impact prognosis and treatment. A tertiary referral centre clinical database was analysed, consisting of 1471 patients with amyotrophic lateral sclerosis seen between 1993 and 2007. Milestones were defined as symptom onset (functional involvement by weakness, wasting, spasticity, dysarthria or dysphagia of one central nervous system region defined as bulbar, upper limb, lower limb or diaphragmatic), diagnosis, functional involvement of a second region, functional involvement of a third region, needing gastrostomy and non-invasive ventilation. Milestone timings were standardized as proportions of time elapsed through the disease course using information from patients who had died by dividing time to a milestone by disease duration. Milestones occurred at predictable proportions of the disease course. Diagnosis occurred at 35% through the disease course, involvement of a second region at 38%, a third region at 61%, need for gastrostomy at 77% and need for non-invasive ventilation at 80%. We therefore propose a simple staging system for amyotrophic lateral sclerosis. Stage 1: symptom onset (involvement of first region); Stage 2A: diagnosis; Stage 2B: involvement of second region; Stage 3: involvement of third region; Stage 4A: need for gastrostomy; and Stage 4B: need for non-invasive ventilation. Validation of this staging system will require further studies in other populations, in population registers and in other clinic databases. The standardized times to milestones may well vary between different studies and populations, although the stages themselves and their meanings are likely to remain unchanged. Oxford University Press 2012-03 2012-01-23 /pmc/articles/PMC3286327/ /pubmed/22271664 http://dx.doi.org/10.1093/brain/awr351 Text en © The Author (2012). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Roche, Jose C.
Rojas-Garcia, Ricardo
Scott, Kirsten M.
Scotton, William
Ellis, Catherine E.
Burman, Rachel
Wijesekera, Lokesh
Turner, Martin R.
Leigh, P. Nigel
Shaw, Christopher E.
Al-Chalabi, Ammar
A proposed staging system for amyotrophic lateral sclerosis
title A proposed staging system for amyotrophic lateral sclerosis
title_full A proposed staging system for amyotrophic lateral sclerosis
title_fullStr A proposed staging system for amyotrophic lateral sclerosis
title_full_unstemmed A proposed staging system for amyotrophic lateral sclerosis
title_short A proposed staging system for amyotrophic lateral sclerosis
title_sort proposed staging system for amyotrophic lateral sclerosis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3286327/
https://www.ncbi.nlm.nih.gov/pubmed/22271664
http://dx.doi.org/10.1093/brain/awr351
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