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Assessment of the validity and reliability of the 32-item Motor Function Measure in individuals with Type 2 or non-ambulant Type 3 spinal muscular atrophy.
Trundell, Dylan; Le Scouiller, Stephanie; Le Goff, Laure; Gorni, Ksenija; Vuillerot, Carole.
Affiliation
  • Trundell D; Roche Products Limited, Welwyn, United Kingdom.
  • Le Scouiller S; Roche Products Limited, Welwyn, United Kingdom.
  • Le Goff L; Department of Pediatric Physical Medicine and Rehabilitation, Hôpital Mère Enfant, CHU-Lyon, Lyon University, Lyon, France.
  • Gorni K; PDMA Neuroscience and Rare Disease, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
  • Vuillerot C; Department of Pediatric Physical Medicine and Rehabilitation, Hôpital Mère Enfant, CHU-Lyon, Lyon University, Lyon, France.
PLoS One ; 15(9): e0238786, 2020.
Article in En | MEDLINE | ID: mdl-32946459
ABSTRACT
The 32-item Motor Function Measure (MFM32) is an assessment of motor function, and its measurement properties were established in a broad neuromuscular disease population. This study sought to investigate the reliability, validity, and ability to detect change of MFM32 in individuals with Type 2 and non-ambulant Type 3 spinal muscular atrophy (SMA). Data were used from the Phase 2 study assessing the efficacy and safety of olesoxime. A total of 110 individuals with Type 2 or 3 SMA were included in the analyses. Test-retest reliability (intraclass-correlation coefficient in global impression-defined stable individuals), internal consistency (Cronbach's alpha), convergent validity (Spearman rank order correlations with other measures), known-groups validity (analysis of covariance comparing Hammersmith Functional Motor Scale -defined groups), and ability to detect change (analysis of covariance comparing global impression-defined groups) were calculated. Strong evidence of test-retest reliability (intraclass-correlation coefficient = 0.93-0.95), internal consistency (Cronbach's alpha = 0.89), convergent validity (Hammersmith Functional Motor Scale rho = 0.87; forced vital capacity rho = 0.61), known-groups validity (all p<0.0001), and ability to detect change (all p<0.001) were demonstrated. These results provide evidence of the MFM32's measurement properties, supporting its use in longitudinal research in individuals with Type 2 and non-ambulant Type 3 SMA.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spinal Muscular Atrophies of Childhood / Cholestenones Type of study: Observational_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: PLoS One Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spinal Muscular Atrophies of Childhood / Cholestenones Type of study: Observational_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: PLoS One Year: 2020 Document type: Article