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Non-neural Muscle Weakness Has Limited Influence on Complexity of Motor Control during Gait.
- Source :
-
Frontiers in human neuroscience [Front Hum Neurosci] 2018 Jan 31; Vol. 12, pp. 5. Date of Electronic Publication: 2018 Jan 31 (Print Publication: 2018). - Publication Year :
- 2018
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Abstract
- Cerebral palsy (CP) and Duchenne muscular dystrophy (DMD) are neuromuscular disorders characterized by muscle weakness. Weakness in CP has neural and non-neural components, whereas in DMD, weakness can be considered as a predominantly non-neural problem. Despite the different underlying causes, weakness is a constraint for the central nervous system when controlling gait. CP demonstrates decreased complexity of motor control during gait from muscle synergy analysis, which is reflected by a higher total variance accounted for by one synergy (tVAF <subscript>1</subscript> ). However, it remains unclear if weakness directly contributes to higher tVAF <subscript>1</subscript> in CP, or whether altered tVAF <subscript>1</subscript> reflects mainly neural impairments. If muscle weakness directly contributes to higher tVAF <subscript>1</subscript> , then tVAF <subscript>1</subscript> should also be increased in DMD. To examine the etiology of increased tVAF <subscript>1</subscript> , muscle activity data of gluteus medius, rectus femoris, medial hamstrings, medial gastrocnemius, and tibialis anterior were measured at self-selected walking speed, and strength data from knee extensors, knee flexors, dorsiflexors and plantar flexors, were analyzed in 15 children with CP [median (IQR) age: 8.9 (2.2)], 15 boys with DMD [8.7 (3.1)], and 15 typical developing (TD) children [8.6 (2.7)]. We computed tVAF <subscript>1</subscript> from 10 concatenated steps with non-negative matrix factorization, and compared tVAF <subscript>1</subscript> between the three groups with a Mann-Whiney U -test. Spearman's rank correlation coefficients were used to determine if weakness in specific muscle groups contributed to altered tVAF <subscript>1</subscript> . No significant differences in tVAF <subscript>1</subscript> were found between DMD [tVAF <subscript>1</subscript> : 0.60 (0.07)] and TD children [0.65 (0.07)], while tVAF <subscript>1</subscript> was significantly higher in CP [(0.74 (0.09)] than in the other groups (both p < 0.005). In CP, weakness in the plantar flexors was related to higher tVAF <subscript>1</subscript> ( r = -0.72). In DMD, knee extensor weakness related to increased tVAF <subscript>1</subscript> ( r = -0.50). These results suggest that the non-neural weakness in DMD had limited influence on complexity of motor control during gait and that the higher tVAF <subscript>1</subscript> in children with CP is mainly related to neural impairments caused by the brain lesion.
Details
- Language :
- English
- ISSN :
- 1662-5161
- Volume :
- 12
- Database :
- MEDLINE
- Journal :
- Frontiers in human neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 29445330
- Full Text :
- https://doi.org/10.3389/fnhum.2018.00005