Your browser doesn't support javascript.
loading
Assessment of the upper limb function, strength, and mobility in treatment-naive children with spinal muscular atrophy Types 2 and 3.
Milev, Evelin; Selby, Victoria; Wolfe, Amy; Rohwer, Annemarie; Tillmann, Ricarda; Ramsey, Danielle; Iodice, Mario; Hogrel, Jean-Yves; Baranello, Giovanni; Scoto, Mariacristina; Muntoni, Francesco.
Afiliación
  • Milev E; Department of Developmental Neuroscience, Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London, UK.
  • Selby V; Department of Neurology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Wolfe A; Department of Developmental Neuroscience, Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London, UK.
  • Rohwer A; Department of Neurology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Tillmann R; Department of Developmental Neuroscience, Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London, UK.
  • Ramsey D; Department of Neurology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Iodice M; Department of Developmental Neuroscience, Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London, UK.
  • Hogrel JY; Department of Neurology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Baranello G; Barts Health NHS Trust, London, UK.
  • Scoto M; School of Health and Sports Sciences, University of Suffolk, Ipswich, UK.
  • Muntoni F; Department of Neurology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Muscle Nerve ; 69(3): 340-348, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38238963
ABSTRACT
INTRODUCTION/

AIMS:

Current upper limb assessments in pediatric spinal muscular atrophy (SMA) may not adequately capture change with disease progression. Our aim was to examine the relationship between motor function, strength, and hand/finger mobility of the upper limb in treatment-naïve children with SMA Types 2 and 3 to assess new methods to supplement current outcomes.

METHODS:

The Revised Upper Limb Module (RULM), grip and pinch strength, and hand/finger mobility data were collected from 19 children with SMA Types 2 and 3 aged 5.2-16.9 years over a year.

RESULTS:

A median loss between 0.5 and 2.5 points in the RULM was seen across all SMA subgroups with the biggest median loss recorded between 10 and 14 years of age. The grip strength loss was -0.06 kg (-4.69 to 3.49; IQR, 1.21); pinch improvement of 0.05 (-0.65 to 1.27; IQR, 0.48); hand/finger mobility test improvement of 4 points (-24 to 14; IQR, 6.75) for the whole cohort. Significant correlations were found between the RULM and grip strength (p < .001), RULM and pinch strength (p < .001), RULM and revised Brooke (p < .001), grip strength and pinch strength (p < .001).

DISCUSSION:

The combined use of the RULM, dynamometry, and hand mobility provide insight about correlations between function and strength in children with SMA. The RULM and grip strength assessments captured a significant decline in upper limb function, whereas the pinch and finger/hand mobility showed an improvement over the course of 1 year and these results should be considered for future studies.
Asunto(s)
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Atrofia Muscular Espinal / Atrofias Musculares Espinales de la Infancia Límite: Adolescent / Child / Humans Idioma: En Revista: Muscle Nerve Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Atrofia Muscular Espinal / Atrofias Musculares Espinales de la Infancia Límite: Adolescent / Child / Humans Idioma: En Revista: Muscle Nerve Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido