4.4 Article

Generation of percentile curves for strength and functional abilities for boys with Duchenne muscular dystrophy

期刊

MUSCLE & NERVE
卷 68, 期 2, 页码 198-205

出版社

WILEY
DOI: 10.1002/mus.27921

关键词

motor function; neuromuscular disorders; rehabilitation; walking; weakness

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This study aimed to describe the clinical manifestations of DMD by developing percentile curves for various measures. The generated curves can help healthcare professionals and caregivers track the progression of the disease in DMD patients.
Introduction/AimsConsidering the heterogeneity of the clinical manifestations of Duchenne muscular dystrophy (DMD), it is important to describe their various clinical profiles. Thus, in this study we aimed to develop percentile curves for DMD using a battery of measures to define the patterns of functional abilities, timed tests, muscle strength, and range of motion (ROM). MethodsThis retrospective data analysis was based on the records of patients with DMD using the Motor Function Measure (MFM) scale, isometric muscle strength (IS), dorsiflexion ROM, 10-meter walk test (10 MWT), and 6-minute walk test (6 MWT). Percentile curves (25th, 50th, and 75th percentiles) with MFM, IS, ROM, 10 MWT, and 6 MWT on the y axis and patient age on the x axis were constructed using the generalized additive model for location, scale, and shape, with Box-Cox power exponential distribution. ResultsThere were records of 329 assessments of patients between 4 and 18 years of age. The MFM percentiles showed a gradual reduction in all dimensions. Muscle strength and ROM percentiles showed that the knee extensors were the most affected from 4 years of age, and dorsiflexion ROM negative values were noted from the age of 8 years. The 10 MWT showed a gradual increase in performance time with age. For the 6 MWT, the distance curve remained stable until 8 years, with a subsequent progressive decline. DiscussionIn this study we generated percentile curves that can help health professionals and caregivers follow the trajectory of disease progression in DMD patients.

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