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Upper limb evaluation and one-year follow up of non-ambulant patients with spinal muscular atrophy: an observational multicenter trial.
Seferian, Andreea Mihaela; Moraux, Amélie; Canal, Aurélie; Decostre, Valérie; Diebate, Oumar; Le Moing, Anne Gaëlle; Gidaro, Teresa; Deconinck, Nicolas; Van Parys, Frauke; Vereecke, Wendy; Wittevrongel, Sylvia; Annoussamy, Mélanie; Mayer, Michèle; Maincent, Kim; Cuisset, Jean-Marie; Tiffreau, Vincent; Denis, Severine; Jousten, Virginie; Quijano-Roy, Susana; Voit, Thomas; Hogrel, Jean-Yves; Servais, Laurent.
Afiliación
  • Seferian AM; Institute of Myology, Paris, France.
  • Moraux A; Institute of Myology, Paris, France.
  • Canal A; Institute of Myology, Paris, France.
  • Decostre V; Institute of Myology, Paris, France.
  • Diebate O; Institute of Myology, Paris, France.
  • Le Moing AG; Institute of Myology, Paris, France; Department of Child Neurology, Centre Hospitalier Universitaire Amiens-Picardie, Amiens, France.
  • Gidaro T; Institute of Myology, Paris, France.
  • Deconinck N; Department of Pediatrics, Division of Pediatric Neurology and Metabolism, Neuromuscular Reference Center, Universitair Ziekenhuis Gent, Gent, Belgium.
  • Van Parys F; Department of Pediatrics, Division of Pediatric Neurology and Metabolism, Neuromuscular Reference Center, Universitair Ziekenhuis Gent, Gent, Belgium.
  • Vereecke W; Department of Pediatrics, Division of Pediatric Neurology and Metabolism, Neuromuscular Reference Center, Universitair Ziekenhuis Gent, Gent, Belgium.
  • Wittevrongel S; Department of Pediatrics, Division of Pediatric Neurology and Metabolism, Neuromuscular Reference Center, Universitair Ziekenhuis Gent, Gent, Belgium.
  • Annoussamy M; Institute of Myology, Paris, France.
  • Mayer M; Reference Center for Neuromuscular Disease, Assistance Publique-Hôpitaux de Paris-Hôpital Trousseau, Paris, France.
  • Maincent K; Reference Center for Neuromuscular Disease, Assistance Publique-Hôpitaux de Paris-Hôpital Trousseau, Paris, France.
  • Cuisset JM; Department of Pediatrics, Centre Hospitalier Régional Universitaire de Lille-Hôpital Roger Salengro, Lille, France.
  • Tiffreau V; Department of Physical Medicine and Rehabilitation, Centre Hospitalier Régional Universitaire de Lille-Hôpital Pierre Swynghedauw, Lille, France.
  • Denis S; Reference Center for Neuromuscular Disease, Centre Hospitalier Régional de La Citadelle, Liège, Belgium.
  • Jousten V; Reference Center for Neuromuscular Disease, Centre Hospitalier Régional de La Citadelle, Liège, Belgium.
  • Quijano-Roy S; Department of Pediatrics, Centre de références Maladies Neuromusculaires Garches-Necker-Mondor-Hendaye and Endicap U1179 INSERM-Université de Versailles-Saint-Quentin-en-Yvelines, Assistance Publique-Hôpitaux de Paris-Hôpital Raymond-Poincaré, Garches, France.
  • Voit T; Institute of Myology, Paris, France; Thérapie des maladies du muscle strié / Institut de Myologie, Unité Mixte de Recherche S 974 Université Pierre et Marie Curie-Institut national de la santé et de la recherche médicale-Formation de Recherche en Evolution 3617 Centre national de la recherche scient
  • Hogrel JY; Institute of Myology, Paris, France.
  • Servais L; Institute of Myology, Paris, France; Reference Center for Neuromuscular Disease, Centre Hospitalier Régional de La Citadelle, Liège, Belgium.
PLoS One ; 10(4): e0121799, 2015.
Article en En | MEDLINE | ID: mdl-25861036
ABSTRACT
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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Atrofia Muscular Espinal / Extremidad Superior Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2015 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Atrofia Muscular Espinal / Extremidad Superior Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2015 Tipo del documento: Article País de afiliación: Francia