Early weight loss in amyotrophic lateral sclerosis: outcome relevance and clinical correlates in a population-based cohort

Cristina Moglia, Andrea Calvo, Maurizio Grassano, Antonio Canosa, Umberto Manera, Fabrizio D'Ovidio, Alessandro Bombaci, Enrica Bersano, Letizia Mazzini, Gabriele Mora, Adriano Chiò, Stefania Cammarosano, Rosario Vasta, Maria Claudia Torrieri, Luca Solero, Marinella Clerico, Stefania De Mercanti, Alessandro Mauro, Luca Pradotto, Fabiola DE MARCHILuisa Sosso, Daniela Leotta, Lucia Appendino, Daniele Imperiale, Roberto Cavallo, Claudio Geda, Fabio Poglio, Paola Santimaria, Umberto Massazza, Antonio Villani, Roberto Conti, Luigi C. Ruiz, Mario Palermo, Franco Vergnano, Eugenia Rota, Maria Teresa Penza, Marco Aguggia, Piero Meineri, Paolo Ghiglione, Nicola Launaro, Giuseppe Astegiano, Giovanni Corso

Risultato della ricerca: Contributo su rivistaArticolo in rivistapeer review

Abstract

Objectives: To assess the role of body mass index (BMI) and of the rate of weight loss as prognostic factors in amyotrophic lateral sclerosis (ALS) and to explore the clinical correlates of weight loss in the early phases of the disease. Methods: The study cohort included all ALS patients in Piemonte/Valle d'Aosta in the 2007-2011 period. Overall survival and the probability of death/tracheostomy at 18 months (logistic regression model) were calculated. Results: Of the 712 patients, 620 (87.1%) were included in the study. Patients ' survival was related to the mean monthly percentage of weight loss at diagnosis (p<0.0001), but not to pre-morbid BMI or BMI at diagnosis. Spinal onset patients with dysphagia at diagnosis had a median survival similar to bulbar onset patients. About 20% of spinal onset patients without dysphagia at diagnosis had severe weight loss and initial respiratory impairment, and had a median survival time similar to bulbar onset patients. Conclusions: The rate of weight loss from onset to diagnosis was found to be a strong and independent prognostic factor in ALS. Weight loss was mainly due to the reduction of nutritional intake related to dysphagia, but a subgroup of spinal onset patients without dysphagia at diagnosis had a severe weight loss and an outcome similar to bulbar patients. According to our findings, we recommend that in clinical trials patients should be stratified according to the presence of dysphagia at the time of enrolment and not by site of onset of symptoms.
Lingua originaleInglese
pagine (da-a)666-673
Numero di pagine8
RivistaJournal of Neurology, Neurosurgery and Psychiatry
Volume90
Numero di pubblicazione6
DOI
Stato di pubblicazionePubblicato - 2019

Keywords

  • Aged
  • Amyotrophic Lateral Sclerosis
  • Body Mass Index
  • Cohort Studies
  • Disease Progression
  • Female
  • Humans
  • Male
  • Survival Analysis
  • Weight Loss
  • amyotrophic lateral sclerosis
  • body mass index
  • dysphagia
  • respiratory function
  • weight loss

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