Amyotrophic lateral sclerosis regional progression intervals change according to time of involvement of different body regions

Author:

Manera Umberto12ORCID,D'Ovidio Fabrizio1ORCID,Cabras Sara1,Torrieri Maria Claudia1ORCID,Canosa Antonio123,Vasta Rosario1,Palumbo Francesca1,Grassano Maurizio1,De Marchi Fabiola4ORCID,Mazzini Letizia4,Mora Gabriele1,Moglia Cristina12ORCID,Calvo Andrea12ORCID,Chiò Adriano123

Affiliation:

1. ALS Centre, “Rita Levi Montalcini” Department of Neuroscience University of Turin Turin Italy

2. Neurology 1, AOU Città della Salute e della Scienza di Torino Turin Italy

3. Institute of Cognitive Sciences and Technologies, C.N.R. Rome Italy

4. ALS Center, Department of Neurology Azienda Ospedaliera Universitaria Maggiore della Carità Novara Italy

Abstract

AbstractBackground and purposeThe prediction of disease course is one of the main targets of amyotrophic lateral sclerosis (ALS) research, particularly considering its wide phenotypic heterogeneity. Despite many attempts to classify patients into prognostic categories according to the different spreading patterns at diagnosis, a precise regional progression rate and the time of involvement of each region has yet to be clarified. The aim of our study was to evaluate the functional decline in different body regions according to their time of involvement during disease course.MethodsIn a population‐based dataset of ALS patients, we analysed the functional decline in different body regions according to time and order of regional involvement. We calculated the regional progression intervals (RPIs) between initial involvement and severe functional impairment using the ALS Functional Rating Scale revised (ALSFRS‐r) subscores for the bulbar, upper limb, lower limb and respiratory/thoracic regions. Time‐to‐event analyses, adjusted for age, sex, ALSFRS‐r pre‐slope (ΔALSFRS‐R), cognitive status, and mutational status were performed.ResultsThe duration of RPI differed significantly among ALS phenotypes, with the RPI of the first region involved being significantly longer than the RPIs of regions involved later. Cox proportional hazard models showed that in fact a longer time between disease onset and initial regional involvement was related to a reduced duration of the RPI duration in each different body region (bulbar region: hazard ratio [HR] 1.11, 95% confidence interval [CI] 1.06–1.16, p < 0.001; upper limb region: HR 1.16, 95% CI 1.06–1.28, p = 0.002; lower limb region: HR 1.11, 95% CI 1.03–1.19, p = 0.009; respiratory/thoracic region: HR 1.10, 95% CI 1.06–1.14, p = 0.005).ConclusionsWe found that the progression of functional decline accelerates in regions involved later during disease course. Our findings can be useful in patient management and prognosis prediction.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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