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A proposed staging system for amyotrophic lateral sclerosis
- Source :
- Brain; Vol 135, BRAIN, r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau, instname, Brain
- Publication Year :
- 2012
- Publisher :
- Oxford University Press, 2012.
-
Abstract
- 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.
- Subjects :
- Male
Pediatrics
medicine.medical_specialty
Weakness
amyotrophic lateral sclerosis
medicine.medical_treatment
Population
Kaplan-Meier Estimate
Cohort Studies
03 medical and health sciences
Sex Factors
0302 clinical medicine
Humans
Medicine
030212 general & internal medicine
Spasticity
Age of Onset
Stage (cooking)
Amyotrophic lateral sclerosis
education
Aged
Gastrostomy
education.field_of_study
Models, Statistical
business.industry
Patient Selection
Reproducibility of Results
Original Articles
staging
Middle Aged
Prognosis
medicine.disease
Respiration, Artificial
Survival Analysis
Dysphagia
3. Good health
natural history
Disease Progression
Physical therapy
motor neuron disease
Female
Neurology (clinical)
medicine.symptom
Age of onset
business
030217 neurology & neurosurgery
El Escorial criteria
Follow-Up Studies
Subjects
Details
- Language :
- English
- ISSN :
- 14602156 and 00068950
- Volume :
- 135
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Brain
- Accession number :
- edsair.doi.dedup.....f8feaedbba774c99aa9185f07e43271e
- Full Text :
- https://doi.org/10.1093/brain/awr351