Revised upper limb module for spinal muscular atrophy: 12 month changes.

Adolescent Adult Algorithms Child Child, Preschool Disease Progression Female Health Status Humans Longitudinal Studies Male Middle Aged Muscular Atrophy, Spinal / pathology Reference Standards Spinal Muscular Atrophies of Childhood / pathology Upper Extremity / pathology Walking Young Adult
Functional assessment Longitudinal Data Neuromuscular disorders Outcome measures Spinal Muscular Atrophy Upper limb

Journal

Muscle & nerve
ISSN: 1097-4598
Titre abrégé: Muscle Nerve
Pays: United States
ID NLM: 7803146

Informations de publication

Date de publication:
04 2019
Historique:
received: 02 09 2018
revised: 15 01 2019
accepted: 19 01 2019
pubmed: 25 1 2019
medline: 6 7 2019
entrez: 25 1 2019
Statut: ppublish

Résumé

The aim of the study was to assess 12 month changes in upper limb function in patients affected by spinal muscular atrophy type 2 and 3. Longitudinal 12 month data was collected in 114 patients, 60 type 2 and 54 type 3, using the Revised Upper Limb Module. The 12 month changes ranged between -7 and 9 (mean: -0.41; SD: 2.93). The mean changes were not significantly different between the three spinal muscular atrophy groups (-0.45 in type 2, -0.23 in non-ambulant type 3 and -0.34 in ambulant type 3, p = 0.96) and the relationship between 12 month change and age classes was not significantly different among the three types of SMA patients. Our results confirm that the Module explores a wide range of functional abilities and can be used in ambulant and non-ambulant patients of different ages in conjunction with other functional scales. Muscle Nerve 59:426-430, 2019.

Identifiants

DOI: 10.1002/mus.26419 PMID: 30677148
pubmed: 30677148
doi: 10.1002/mus.26419
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

426-430

Subventions

Organisme : Eunice Kennedy Shriver National Institute of Child Health and Human Development
ID : K01HD084690-02
Pays : International
Organisme : Fondazione Telethon
ID : GSP13002
Pays : International
Organisme : MDUK
ID : 13/LO/1748
Pays : International
Organisme : MDUK
ID : 513395
Pays : International
Organisme : MRC Translational Research Centre
ID : MR/K501074/1
Pays : International
Organisme : Muscular Dystrophy UK Centre
ID : 07DN02
Pays : International
Organisme : Muscular Dystrophy UK Centre
ID : 37787
Pays : International
Organisme : Spinal Muscular Atrophy Foundation
Pays : International
Organisme : The SMA Trust
Pays : International

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Maria Carmela Pera (MC)

Paediatric Neurology and Centro Clinico Nemo, Catholic University and Policlinico Gemelli, Fondazione Policlinico Universitario Agostino Gemelli IRCSS, Rome, Italy.

Giorgia Coratti (G)

Paediatric Neurology and Centro Clinico Nemo, Catholic University and Policlinico Gemelli, Fondazione Policlinico Universitario Agostino Gemelli IRCSS, Rome, Italy.

Elena S Mazzone (ES)

Paediatric Neurology and Centro Clinico Nemo, Catholic University and Policlinico Gemelli, Fondazione Policlinico Universitario Agostino Gemelli IRCSS, Rome, Italy.

Jacqueline Montes (J)

Departments of Rehabilitation and Regenerative Medicine, Columbia University Medical Center, New York, USA.
Departments of Neurology, Columbia University Medical Center, New York, USA.

Mariacristina Scoto (M)

Dubowitz Neuromuscular Centre and NIHR Great Ormond Street Hospital Biomedical Research Centre, Institute of Child Health & Great Ormond Street Hospital, London, UK.

Roberto De Sanctis (R)

Paediatric Neurology and Centro Clinico Nemo, Catholic University and Policlinico Gemelli, Fondazione Policlinico Universitario Agostino Gemelli IRCSS, Rome, Italy.

Marion Main (M)

Dubowitz Neuromuscular Centre and NIHR Great Ormond Street Hospital Biomedical Research Centre, Institute of Child Health & Great Ormond Street Hospital, London, UK.

Anna Mayhew (A)

John Walton Muscular Dystrophy Research Centre, Newcastle University, UK.

Robert Muni Lofra (R)

John Walton Muscular Dystrophy Research Centre, Newcastle University, UK.

Sally Dunaway Young (S)

Departments of Rehabilitation and Regenerative Medicine, Columbia University Medical Center, New York, USA.
Departments of Neurology, Columbia University Medical Center, New York, USA.

Allan M Glanzman (AM)

Department of Physical Therapy, The Children's Hospital of Philadelphia, Philadelphia.

Tina Duong (T)

Department of Neurology, Stanford University, Stanford, California, USA.

Amy Pasternak (A)

Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Department of Physical Therapy and Occupational Therapy, Boston Children's Hospital, Boston, MA, USA.
ORCID: 0000-0001-8841-2613

Danielle Ramsey (D)

Dubowitz Neuromuscular Centre and NIHR Great Ormond Street Hospital Biomedical Research Centre, Institute of Child Health & Great Ormond Street Hospital, London, UK.

Basil Darras (B)

Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

John W Day (JW)

Department of Neurology, Stanford University, Stanford, California, USA.

Richard S Finkel (RS)

Nemours Children's Hospital, University of Central Florida College of Medicine, Orlando, USA.

Darryl C De Vivo (DC)

Departments of Neurology, Columbia University Medical Center, New York, USA.

Maria Pia Sormani (MP)

Department of Health Sciences (DISSAL), Section of Biostatistics, University of Genova, Genova, Italy.

Francesca Bovis (F)

Department of Health Sciences (DISSAL), Section of Biostatistics, University of Genova, Genova, Italy.

Volker Straub (V)

John Walton Muscular Dystrophy Research Centre, Newcastle University, UK.

Francesco Muntoni (F)

Dubowitz Neuromuscular Centre and NIHR Great Ormond Street Hospital Biomedical Research Centre, Institute of Child Health & Great Ormond Street Hospital, London, UK.

Marika Pane (M)

Paediatric Neurology and Centro Clinico Nemo, Catholic University and Policlinico Gemelli, Fondazione Policlinico Universitario Agostino Gemelli IRCSS, Rome, Italy.

Eugenio Mercuri (E)

Paediatric Neurology and Centro Clinico Nemo, Catholic University and Policlinico Gemelli, Fondazione Policlinico Universitario Agostino Gemelli IRCSS, Rome, Italy.

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Classifications MeSH

questionsmedicales.fr › Personnes › Tranches d'âge › Adolescent › Revised upper limb module for spinal muscular...
questionsmedicales.fr › Personnes › Tranches d'âge › Adulte › Revised upper limb module for spinal muscular...
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questionsmedicales.fr › Personnes › Tranches d'âge › Enfant › Enfant d'âge préscolaire › Revised upper limb module for spinal muscular...
questionsmedicales.fr › États, signes et symptômes pathologiques › Processus pathologiques › Caractéristiques de la maladie › Évolution de la maladie › Revised upper limb module for spinal muscular...
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questionsmedicales.fr › Maladies du système nerveux › Maladies neuromusculaires › Maladies du motoneurone › Amyotrophie spinale › Revised upper limb module for spinal muscular...
questionsmedicales.fr › Techniques d'investigation › Poids et mesures › Normes de référence › Revised upper limb module for spinal muscular...
questionsmedicales.fr › Malformations et maladies congénitales, héréditaires et néonatales › Maladies génétiques congénitales › Maladies neurodégénératives héréditaires › Amyotrophies spinales infantiles › Revised upper limb module for spinal muscular...
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