Literature DB >> 25540220

Decomposition of surface EMG signals from cyclic dynamic contractions.

Carlo J De Luca1, Shey-Sheen Chang2, Serge H Roy3, Joshua C Kline4, S Hamid Nawab5.   

Abstract

Over the past 3 decades, various algorithms used to decompose the electromyographic (EMG) signal into its constituent motor unit action potentials (MUAPs) have been reported. All are limited to decomposing EMG signals from isometric contraction. In this report, we describe a successful approach to decomposing the surface EMG (sEMG) signal collected from cyclic (repeated concentric and eccentric) dynamic contractions during flexion/extension of the elbow and during gait. The increased signal complexity introduced by the changing shapes of the MUAPs due to relative movement of the electrodes and the lengthening/shortening of muscle fibers was managed by an incremental approach to enhancing our established algorithm for decomposing sEMG signals obtained from isometric contractions. We used machine-learning algorithms and time-varying MUAP shape discrimination to decompose the sEMG signal from an increasingly challenging sequence of pseudostatic and dynamic contractions. The accuracy of the decomposition results was assessed by two verification methods that have been independently evaluated. The firing instances of the motor units had an accuracy of ∼90% with a MUAP train yield as high as 25. Preliminary observations from the performance of motor units during cyclic contractions indicate that during repetitive dynamic contractions, the control of motor units is governed by the same rules as those evidenced during isometric contractions. Modifications in the control properties of motoneuron firings reported by previous studies were not confirmed. Instead, our data demonstrate that the common drive and hierarchical recruitment of motor units are preserved during concentric and eccentric contractions.
Copyright © 2015 the American Physiological Society.

Keywords:  dynamic contractions; firing rate; gait; motor units

Mesh:

Year:  2014        PMID: 25540220      PMCID: PMC4359986          DOI: 10.1152/jn.00555.2014

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


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Authors:  C J De Luca; R S LeFever; M P McCue; A P Xenakis
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