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The most bothersome symptoms in neuromuscular diseases: the ERN EURO NMD Survey

  • Michelangelo Mancuso*
  • , Alessandro Colitta
  • , Manuela Lavorato
  • , Peter van den Bergh
  • , Janbernd Kirschner
  • , Cornelia Kornblum
  • , Lorenzo Maggi
  • , Francois Lamy
  • , Hanns Lochmüller
  • , Marianne Nordstrøm
  • , Edoardo Malfatti
  • , Alessandra Ferlini
  • , Davide Pareyson
  • , Vincenzo Silani
  • , Kleopas A. Kleopa
  • , Marianne de Visser
  • , Antonio Atalaia
  • , Teresinha Evangelista
  • *Corresponding author for this work
  • University of Pisa
  • Azienda Ospedaliero-Universitaria Pisana
  • Université catholique de Louvain
  • University of Freiburg
  • University of Bonn
  • IRCCS Fondazione Istituto Neurologico Carlo Besta - Milano
  • AFM-Téléthon
  • Centro Nacional de Análisis Genómico (CNAG)
  • University of Ottawa
  • University of Oslo
  • Frambu Resource Centre for Rare Disorders
  • Université Paris-Est Créteil Val de Marne
  • University of Ferrara
  • IRCCS Istituto Auxologico Italiano - Milano
  • University of Milan
  • Cyprus Institute of Neurology and Genetics
  • Amsterdam UMC - University of Amsterdam
  • Centre de Recherche en Myologie
  • Sorbonne Université

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Background: Neuromuscular diseases (NMDs) comprise a range of genetic and acquired rare disorders that affect motor neurons, peripheral nerves, neuromuscular junctions and skeletal muscles, leading to significant impairments such as muscle weakness and fatigue resulting in functional limitations. This study aims to investigate the prevalence and severity of disease-related symptoms in adult patients with NMDs registered in the European Reference Network (ERN) EURO-NMD. A cross-sectional electronic survey was conducted with 1,253 participants who reported the severity of 28 symptoms, which were scored using multi-criteria decision analysis (MCDA). Results: The results identified muscle fatigue, weakness and impaired physical function/activity as the most severe and prevalent symptoms in all NMD groups, followed by coordination and/or balance problems, muscle stiffness, mental fatigue, and pain. Notably, the analysis highlighted differences in symptom severity between disease subtypes and underlined the need for standardised patient-reported outcome measures (PROMs) to address the broad heterogeneity of NMDs. Conclusions: The findings stress the critical importance of capturing patient perspectives to guide clinical care, research priorities and therapeutic development. This work argues for the development of uniform PROMs to better assess disease impact, natural history and treatment efficacy, contributing to improved patient-centred care across diverse NMD populations.
Original languageEnglish
Article number221
JournalOrphanet journal of rare diseases
Volume20
Issue number1
DOIs
Publication statusPublished - 1 Dec 2025

Keywords

  • Neuromuscular diseases
  • PROMs
  • Symptoms

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