PLoS ONE (Jan 2015)

Upper limb evaluation and one-year follow up of non-ambulant patients with spinal muscular atrophy: an observational multicenter trial.

  • Andreea Mihaela Seferian,
  • Amélie Moraux,
  • Aurélie Canal,
  • Valérie Decostre,
  • Oumar Diebate,
  • Anne Gaëlle Le Moing,
  • Teresa Gidaro,
  • Nicolas Deconinck,
  • Frauke Van Parys,
  • Wendy Vereecke,
  • Sylvia Wittevrongel,
  • Mélanie Annoussamy,
  • Michèle Mayer,
  • Kim Maincent,
  • Jean-Marie Cuisset,
  • Vincent Tiffreau,
  • Severine Denis,
  • Virginie Jousten,
  • Susana Quijano-Roy,
  • Thomas Voit,
  • Jean-Yves Hogrel,
  • Laurent Servais

DOI
https://doi.org/10.1371/journal.pone.0121799
Journal volume & issue
Vol. 10, no. 4
p. e0121799

Abstract

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Assessment of the upper limb strength in non-ambulant neuromuscular patients remains challenging. Although potential outcome measures have been reported, longitudinal data demonstrating sensitivity to clinical evolution in spinal muscular atrophy patients are critically lacking. Our study recruited 23 non-ambulant patients, 16 patients (males/females = 6/10; median age 15.4 years with a range from 10.7 to 31.1 years) with spinal muscular atrophy type II and 7 patients (males/females = 2/5; median age 19.9 years with a range from 8.3 to 29.9 years) with type III. The Brooke functional score was on median 3 with a range from 2 to 6. The average total vital capacity was 46%, and seven patients required non-invasive ventilation at night. Patients were assessed at baseline, 6 months, and 1 year using the Motor Function Measure and innovative devices MyoGrip, MyoPinch, and MoviPlate, which assess handgrip strength, key pinch strength, and hand/finger extension-flexion function, respectively. The study demonstrated the feasibility and reliability of these measures for all patients, and sensitivity to negative changes after the age of 14 years. The younger patients showed an increase of the distal force in the follow-up period. The distal force measurements and function were correlated to different functional scales. These data represent an important step in the process of validating these devices as potential outcome measures for future clinical trials.