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BACKGROUND: Measurement of muscle strength and motor function is recommended in clinical trials of neuromuscular diseases, but the loss of hand strength at which motor function is impacted is not documented. OBJECTIVES: To establish the relationship between hand strength and function, and to determine the strength threshold that differentiates normal and abnormal hand function in individuals with Duchenne Muscular Dystrophy (DMD) or Spinal Muscular Atrophy (SMA). METHODS: Maximal handgrip and key pinch strength were measured with the MyoGrip and MyoPinch dynamometers, respectively. Hand function was assessed using the MoviPlate, the Motor Function Measure items for distal upper limb (MFM-D3-UL) and the Cochin Hand Function Scale (CHFS). RESULTS: Data from 168 participants (91 DMD and 77 SMA, age 6-31 years) were analyzed. Relationships between strength and function were significant (P 

Original publication

DOI

10.3233/JND-230182

Type

Journal article

Journal

J Neuromuscul Dis

Publication Date

2024

Volume

11

Pages

777 - 790

Keywords

Hand, duchenne, muscular dystrophy, patient outcome assessment, spinal muscular atrophy, Humans, Muscular Dystrophy, Duchenne, Hand Strength, Male, Adolescent, Child, Muscular Atrophy, Spinal, Adult, Young Adult, Female, Clinical Trials as Topic, Muscle Strength Dynamometer