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Published on: April 18, 2011
Multi-scale complexity analysis of muscle coactivation during gait in children with cerebral palsy
Wen Tao1, Xu Zhang1, Xiang Chen1
1Neuromuscular Control Laboratory, Department of Electronic Science and Technology, University of Science and Technology of China Hefei, China.
Insights
This study used advanced analysis to examine muscle coordination in children with cerebral palsy (CP) during walking. Results show unique complexity patterns in CP, offering insights into neuropathology and motor function assessment.
Area of Science:
- Biomedical Engineering
- Neuroscience
- Rehabilitation Science
Background:
- Cerebral palsy (CP) affects motor control, impacting gait and muscle coordination.
- Understanding the complexity of muscle coactivation during gait is crucial for CP assessment.
- Existing methods may not fully capture the nuanced dynamics of muscle activity in CP.
Purpose of the Study:
- To characterize lower-extremity muscle coactivation and coordination complexity during gait in children with CP.
- To compare gait muscle coordination complexity between children with CP, typically developing (TD) children, and healthy adults.
- To apply multivariate multi-scale entropy (MMSE) analysis to surface electromyographic (EMG) signals for novel insights into CP neuropathology.
Main Methods:
- Collected 16-channel surface EMG data from thigh and lower leg muscles during walking in 11 CP children, 8 TD children, and 7 healthy adults.
- Processed EMG data using multivariate empirical mode decomposition (MEMD) for aligned data scales.
- Applied multivariate multi-scale entropy (MMSE) analysis across 14 schemes varying muscle combinations and time durations.
Main Results:
- Typically developing children and healthy adults exhibited consistent MMSE curves, indicating stable muscle coactivation complexity.
- Children with CP displayed distinct and diverse MMSE curve patterns compared to the control group.
- Abnormal complexity patterns in CP were linked to motor control impairments, altered muscle couplings, spasticity, or paralysis.
Conclusions:
- CP is associated with altered dynamical complexity of muscle coactivation and coordination during gait.
- Neuropathological processes in CP manifest as diverse muscle activation patterns.
- This novel approach may lead to quantitative indices for assessing muscle activation and motor function in CP.
- Findings expand understanding of CP neuropathology through the lens of muscle co-activation complexity.
Abstract:
The objective of this study is to characterize complexity of lower-extremity muscle coactivation and coordination during gait in children with cerebral palsy (CP), children with typical development (TD) and healthy adults, by applying recently developed multivariate multi-scale entropy (MMSE) analysis to surface electromyographic (EMG) signals. Eleven CP children (CP group), eight TD children and seven healthy adults (considered as an entire control group) were asked to walk while surface EMG signals were collected from five thigh muscles and three lower leg muscles on each leg (16 EMG channels in total). The 16-channel surface EMG data, recorded during a series of consecutive gait cycles, were simultaneously processed by multivariate empirical mode decomposition (MEMD), to generate fully aligned data scales for subsequent MMSE analysis. In order to conduct extensive examination of muscle coactivation complexity using the MEMD-enhanced MMSE, 14 data analysis schemes were designed by varying partial muscle combinations and time durations of data segments. Both TD children and healthy adults showed almost consistent MMSE curves over multiple scales for all the 14 schemes, without any significant difference (p > 0.09). However, distinct diversity in MMSE curve was observed in the CP group when compared with the control group. There appears to be diverse neuropathological processes in CP that may affect dynamical complexity of muscle coactivation and coordination during gait. The abnormal complexity patterns emerging in the CP group can be attributed to different factors such as motor control impairments, loss of muscle couplings, and spasticity or paralysis in individual muscles. This study expands our knowledge of neuropathology of CP from a novel point of view of muscle co-activation complexity, which might be useful to derive a quantitative index for assessing muscle activation characteristics as well as motor function in CP.
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