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Different trajectories in upper limb and gross motor function in spinal muscular atrophy.
Coratti, Giorgia; Pera, Maria Carmela; Montes, Jacqueline; Pasternak, Amy; Scoto, Mariacristina; Baranello, Giovanni; Messina, Sonia; Dunaway Young, Sally; Glanzman, Allan M; Duong, Tina; De Sanctis, Roberto; Mazzone, Elena Stacy; Milev, Evelin; Rohwer, Annemarie; Civitello, Matthew; Pane, Marika; Antonaci, Laura; Frongia, Anna Lia; Sframeli, Maria; Vita, Gian Luca; DʼAmico, Adele; Mizzoni, Irene; Albamonte, Emilio; Darras, Basil T; Bertini, Enrico; Sansone, Valeria A; Bovis, Francesca; Day, John; Bruno, Claudio; Muntoni, Francesco; De Vivo, Darryl C; Finkel, Richard; Mercuri, Eugenio.
Afiliación
  • Coratti G; Pediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Pera MC; Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
  • Montes J; Pediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Pasternak A; Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
  • Scoto M; Departments of Rehabilitation and Regenerative Medicine and Neurology, Columbia University Irving Medical Center, New York, New York, USA.
  • Baranello G; Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, United States.
  • Messina S; Dubowitz Neuromuscular Centre, UCL Institute of Child Health & Great Ormond Street Hospital, London, UK.
  • Dunaway Young S; Dubowitz Neuromuscular Centre, UCL Institute of Child Health & Great Ormond Street Hospital, London, UK.
  • Glanzman AM; Department of Clinical and Experimental Medicine and Centro Clinico Nemo Sud, University of Messina, Messina, Italy.
  • Duong T; Department of Neurology, Stanford University, Stanford, California, USA.
  • De Sanctis R; Department of Physical Therapy, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Mazzone ES; Department of Neurology, Stanford University, Stanford, California, USA.
  • Milev E; Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
  • Rohwer A; Pediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Civitello M; Dubowitz Neuromuscular Centre, UCL Institute of Child Health & Great Ormond Street Hospital, London, UK.
  • Pane M; Dubowitz Neuromuscular Centre, UCL Institute of Child Health & Great Ormond Street Hospital, London, UK.
  • Antonaci L; St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Frongia AL; Pediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Sframeli M; Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
  • Vita GL; Pediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
  • DʼAmico A; Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
  • Mizzoni I; Pediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Albamonte E; Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
  • Darras BT; Department of Clinical and Experimental Medicine and Centro Clinico Nemo Sud, University of Messina, Messina, Italy.
  • Bertini E; Department of Clinical and Experimental Medicine and Centro Clinico Nemo Sud, University of Messina, Messina, Italy.
  • Sansone VA; Unit of Neuromuscular and Neurodegenerative Disorders, Department of Neurosciences, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.
  • Bovis F; Unit of Neuromuscular and Neurodegenerative Disorders, Department of Neurosciences, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.
  • Day J; Neurorehabilitation Unit, University of Milan, Neuromuscular Omnicentre Clinical Center, Niguarda Hospital, Milan, Italy.
  • Bruno C; Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, United States.
  • Muntoni F; Unit of Neuromuscular and Neurodegenerative Disorders, Department of Neurosciences, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.
  • De Vivo DC; Neurorehabilitation Unit, University of Milan, Neuromuscular Omnicentre Clinical Center, Niguarda Hospital, Milan, Italy.
  • Finkel R; Biostatistics Unit, Department of Health Sciences, University of Genoa, Genoa, Italy.
  • Mercuri E; Department of Neurology, Stanford University, Stanford, California, USA.
Muscle Nerve ; 64(5): 552-559, 2021 11.
Article en En | MEDLINE | ID: mdl-34327716
INTRODUCTION: The Hammersmith Functional Motor Scale Expanded (HFMSE) and the Revised Upper Limb Module (RULM) have been widely used in natural history studies and clinical trials. Our aim was to establish how the scales relate to each other at different age points in spinal muscular atrophy (SMA) type 2 and 3, and to describe their coherence over 12 mo. METHODS: The study was performed by cross-sectional and longitudinal reanalysis of previously published natural history data. The longitudinal analysis of the 12-mo changes also included the analysis of concordance between scales with changes grouped as stable (±2 points), improved (>+2) or declined (>-2). RESULTS: Three hundred sixty-four patients were included in the cross-sectional analysis, showing different trends in score and point of slope change for the two scales. For type 2, the point of slope change was 4.1 y for the HFMSE and 5.8 for the RULM, while for type 3, it was 6 y for the HFMSE and 7.3 for the RULM. One-hundred-twenty-one patients had at least two assessments at 12 mo. Full concordance was found in 57.3% of the assessments, and in 40.4% one scale remained stable and the other changed. Each scale appeared to be more sensitive to specific age or functional subgroups. DISCUSSION: The two scales, when used in combination, may increase the sensitivity to detect clinically meaningful changes in motor function in patients with SMA types 2 and 3.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Atrofia Muscular Espinal / Atrofias Musculares Espinales de la Infancia Tipo de estudio: Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Muscle Nerve Año: 2021 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Atrofia Muscular Espinal / Atrofias Musculares Espinales de la Infancia Tipo de estudio: Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Muscle Nerve Año: 2021 Tipo del documento: Article País de afiliación: Italia