Cloud Computing Cloud Computing PaaS Techniques File System.
[IEEE 2009 Digital Image Computing: Techniques and Applications - Melbourne, Australia...
Transcript of [IEEE 2009 Digital Image Computing: Techniques and Applications - Melbourne, Australia...
Estimation of Muscle fatigue during cyclic contractions using source separation
techniques
Ganesh R. Naik, Dinesh K. Kumar, Katherine Wheeler, Sridhar P. Arjunan
School of Electrical and Computer Engineering
RMIT Univerisity
Melbourne, Australia
Email: [email protected]
Abstract—Previous research studies have reported that spec-tral compression of the surface Electromyogram (SEMG)towards lower frequencies is associated with onset of localizedmuscle fatigue. One reason for this spectral compression hasbeen attributed to motor unit synchronization in literature.According to this, motor units are pseudo randomly ex-cited during muscle contraction, and the recruitment patternchanges during the onset of muscle fatigue, such that the firingof motor units becomes more synchronized. While this theoryis widely accepted, there is little experimental proof of the phe-nomenon. This paper has used source dependence propertiesand measures developed in research related to independentcomponent analysis (ICA) to test for synchronization. Thispaper has also determined that the global matrix can be usedas a measure for estimating localized muscle fatigue duringcyclic movements.
Keywords-Surface EMG; Muscle fatigue; Source separation;ICA;
I. INTRODUCTION
Muscle fibers are organized in the muscle into motor
units, with a single motor unit consisting of a motor neuron
and muscle fibers innervated by this neuron. Contraction of
muscle fibers is associated with action potentials and these
cause measurable changes of the electrical potential at the
surface of the body. The recording of the electrical potential
from the surface is surface electromyogram (sEMG). The
combination of muscle fiber action potential from all muscle
fibers of a motor unit is the motor unit action potential
(MUAP). The amplitude of the MUAP depends upon the
types, sizes and number of muscle fibers in the motor unit.
SEMG is the result of the interferential summation of all
MUAPs in the recording field. These potentials are non-
linearly attenuated by cutaneous tissue between the muscle
and the surface electrode. This attenuation is frequency
dependent [1], [2]. Despite the complex nature of the signal,
the SEMG can be used to identify level of muscle contrac-
tion,neuromuscular diseases, abnormal muscle activity and
muscle fatigue.
Muscle fatigue is the state of the muscle when the ability
of a skeletal muscle to contract or produce force is highly
diminished. The causes of fatigue vary, and can be located
anywhere in the neuromuscular path between the brain
and the muscle itself. Local muscle fatigue occurs when
the neuro stimulation path is intact, but the ability of the
muscle to produce force is reduced. The known causes
of local muscle fatigue vary, and depend on the level of
muscle activity and the muscle fiber types present. Localized
muscle fatigue generally results after sustained or intense
contractions.
Numerous researchers have studied muscle fatigue and
the effect of muscle fatigue on the SEMG signal. The
predominant effects of fatigue on the SEMG during high
level contractions are (i) an increase in the signal ampli-
tude and (ii) compression of the spectrum towards lower
frequencies. Well-studied and accepted features of the sEMG
signal for fatigue assessment include amplitude features
[3](Root mean square (RMS) and integrated EMG (iEMG))
or spectral features (mean or median frequency (MDF) or
power spectral density (PSD)) [4]. These general trends
can be partly explained by understanding the physiological
effects of local muscle fatigue.
Firstly, fatigue results in the slowing of the average
action potential conduction velocity due to a buildup of
the byproduct lactic acid. This has been considered to be
the predominant cause of the spectral compression of the
SEMG towards lower frequencies [5]. Secondly, an increase
in the muscle cell hyper polarization time due to the onset
of localized muscle fatigue changes the shape of the action
potential. The general effect of this is a slight displacement
towards lower frequencies.
The other impact of sustained contraction leads to the
recruitment of muscle fibres usually active only during rapid
contractions. The recruitment of these larger muscle fibres
results in an increase in the average SEMG amplitude.
Finally, muscle fatigue can affect motor unit recruitment pat-
terns [6], [7]. Recruitment changes and motor units appear
to become synchronized with the onset of localized muscle
fatigue. This increased synchronicity of motor unit firing
also results in a spectrum shift towards lower frequencies.
However, the total effect of this increase in synchronicity is
not known and warrants further investigation.
Modeling studies have found that the spectral shift to
lower frequencies (and the related drop in MDF) is coun-
2009 Digital Image Computing: Techniques and Applications
978-0-7695-3866-2/09 $26.00 © 2009 IEEE
DOI 10.1109/DICTA.2009.43
225
2009 Digital Image Computing: Techniques and Applications
978-0-7695-3866-2/09 $26.00 © 2009 IEEE
DOI 10.1109/DICTA.2009.43
209
2009 Digital Image Computing: Techniques and Applications
978-0-7695-3866-2/09 $26.00 © 2009 IEEE
DOI 10.1109/DICTA.2009.43
217
2009 Digital Image Computing: Techniques and Applications
978-0-7695-3866-2/09 $26.00 © 2009 IEEE
DOI 10.1109/DICTA.2009.43
217
tered by a reduction in the conduction velocity (CV) [7].
During low-level bicep voluntary contractions, MF also
drops, but the CV remains the same. With the onset of
fatigue, the motor unit firing patterns become significantly
more synchronous (firing at almost the same time). In the
fatigue state, the central drive to a muscle has to increase,
leading to synaptic input that is common to more than one
neuron. This leads to increased synchronicity. Kleine et al
[6] posits that changes in the firing pattern, particularly
synchronization, must be responsible for the spectral shift to
lower frequencies not attributable to a conduction velocity
change.
While widely accepted, there appears to be lack of di-
rect evidence of the synchronization of motor units during
localized muscle fatigue [8]. Further, the effects of such syn-
chronization on the sEMG signal are not yet confirmed, with
signal dependence [9], recurrence quantification analysis [8]
and cross correlation of motor unit pairs [10] all reported as
methods of quantifying motor unit synchronisation.
Recent experimental studies on synchronicity have fo-
cussed on constant force, isometric contractions of the bicep
[8]–[10]. In order to be applicable in real world scenarios,
an understanding of the changes in synchronicity, and the
effect of these changes on the SEMG during dynamic or
cyclic movements must also be sought.
During dynamic contractions, the frequency content of
the SEMG changes continually due to the modulation of the
muscle force and the relative displacement of muscle force
with respect to the underlying muscle fibers. Therefore, fre-
quency analysis techniques for stationary techniques are not
suitable. Bonato et al [11] detailed time-frequency analysis
techniques for assessing local muscle fatigue during cyclic
contractions. An alternative to such complex techniques
would be to investigate features of the SEMG signal which
are not dependent on the frequency content of the signal.
It has recently been demonstrated [9] that there exists
motor unit synchronization due to the onset of fatigue
demonstrated with channel dependence. If synchronicity is
due to an increase in the central drive to a muscle, then
the hypothesis that this would lead to an increase in motor
unit dependence appears sound. In the non-fatigued state,
motor units will fire pseudo-randomly, such that sEMG
recorded from two recording sites should be independent
from each other. This was confirmed using experimental
isometric contraction data.
Further, it was shown that as local muscle fatigue in-
creased, the dependence of the recorded signals on each
other also increased [9]. This paper reports the research
that attempts to characterize the effects of fatigue during
cyclic movements (repeated supination and pronation of the
forearm) of the human arm using Independent Component
Analysis (ICA) techniques.
II. THEORY
A. ICA theory
Independent Component Analysis (ICA) is an iterative
technique used to estimate statistically independent source
signals s(t) = [s1(t), ....,sn(t)]Tfrom a given set of their
linear mixtures x(t) = [x1(t), ....,xn(t)]. If the mixing processis assumed to be linear, it can be expressed as
x(t) = As(t) (1)
where A is an N ×M scalar matrix representing the
unknown mixing coefficients. A is referred to as the transfer
or mixing matrix. The goal of ICA is to find a linear
transformation W of the dependent sensor signals x(t) thatmakes the outputs as independent as possible:
s(t) =Wx(t) =WAs(t) (2)
where s(t) is an estimate of the sources. The sources are
exactly recovered whenW is the inverse of A subject to order
permutation and scale change. Since both, the sources and
the mixing coefficients are unknown, it is impossible either
to determine the variances or the order of the independent
components.
The product of the mixing matrix, A, with the estimated
unmixing matrix, W , is the global matrix, G. After sorting
the order ambiguity between the mixing and unmixing
matrix, under ideal conditions, this global matrix, G should
be a unity matrix and the determinant of this should be
unity [12], [13]. However, if the recordings are not all
independent, the determinant of this matrix is no longer unity
and is close to zero. This can be used as an indicator of the
dependence of the input to the system.
One shortcoming of the above is that this requires prior
knowledge of the mixing matrix, which in real situations is
not possible. To estimate G, one option is to use sub-band
ICA.
B. Sub-band ICA
Sub-band ICA is an extension of ICA. It assumes that
each source is represented as the sum of some independent
sub components and dependent sub components, which have
different frequency bands. Wide-band source signals are a
linear decomposition of several narrow-band sub compo-
nents s(t) = s1(t)+ ....+ sn(t). Such decomposition can be
modeled in the time, frequency or time frequency domains
using any suitable linear transform.
We obtain a set of un-mixing or separating matrices:
W1,W2, ....,Wn where W1 is the un-mixing matrix for sensor
data x1(t) and Wn is the un-mixing matrix for sensor data
xn(t). If the specific sub-components of interest are mutuallyindependent for at least two sub-bands, or more generally
two subsets of multi-band, such as for the sub band ‘p’ and
sub band ‘q’, then the global matrix
Gpq =Wp×W−1q = P (3)
226210218218
will be a sparse generalized permutation matrix P with
special structure with only one non-zero (or strongly domi-
nating) element in each row and each column [14].
III. METHODOLOGY
A. SEMG Recording Equipment
Surface electromyogram (SEMG) signals were recorded
using BIOPAC 100 (California, USA), a proprietary SEMG
acquisition system. Prior to placing the electrodes the par-
ticipants’ skin was cleaned using mild soap. The following
parameters were used during the recording:
• Preamplifier Gain: 2000
• Low Pass Filter: 500Hz
• High Pass Filter: 10Hz
• Notch Filter: 50dB@50Hz
• Sampling frequency: 1500
Two-channel SEMG were recorded from biceps muscles
using surface electrodes during isometric contractions.
B. Experimental Protocol
Four healthy volunteer subjects participated in the trial.
The experimental protocol was approved by the Human
Ethics Committee of RMIT University. Electrode pairs were
placed longitudinally, and the two pairs of electrodes were
placed such that each pair was on either side of the midline
of the biceps muscle (medial and lateral belly) Each subject
performed repeated cyclic contraction using fixed standard
load. The load was chosen to be close to 75% maximum
voluntary contraction. The SEMG was recorded throughout
the experiment until the subject complained of muscle
fatigue. The typical time period of each recording was 180
seconds.
C. Data Analysis
Firstly, the following three data subsets(as shown in
Figure 1) were extracted for analysis:
1) During the beginning of the cyclic experiment (Where
it is assumed that the muscle unit firings are indepen-
dent from each other)
2) In the middle of the cyclic experiment. The intent here
was to test the trend of independency and dependency
3) At the final stages of the cyclic experiment to test the
quality of the source separation and the muscle fatigue
levels.
The three SEMG subsets were analyzed using ICA tech-
niques to detect localized muscle fatigue. This was done
using two signal processing techniques.
1) Preliminary analysis using RMS: Initially the FastICA
MATLAB software was used to separate the sources. This is
a known application of ICA, used to reduce crosstalk prior to
calculating the amplitude features (RMS). The RMS values
were computed for all three described data subsets.
2) Global matrix analysis: The determinant of global
matrix generated using ICA is used as an indicator for iden-
tifying the muscle fatigue. This analysis was also performed
for the three different conditions.
IV. RESULTS AND OBSERVATIONS
The results of the data analysis are tabulated in Tables
I and II. Table I shows the RMS values of SEMG (2
channels) for the initial, middle and final segments of the
cyclic contraction data after source separation using ICA.
Table II shows the value of the determinant of the global
matrix, calculated to determine the dependency and the
independency properties using ICA.
From Table I and Figure 2, it is evident that the RMS of
both channels increases as a result of the onset of muscle
fatigue. This confirms that onset of muscle fatigue results in
the recruitment of larger and faster motor units. However,
these do not shed any light regarding the dependency or
synchronicity behaviour of the motor units due to the onset
of localised muscle fatigue.
Table IRMS OF THE ICA SEPARATED SOURCES
Subject Beginning data Middle data End data
Ch 1 Ch 2 Ch 1 Ch 2 Ch 1 Ch 2
1 1.001 1.142 1.289 1.217 1.419 1.415
2 1.125 1.115 1.201 1.300 1.402 1.456
3 1.210 1.206 1.210 1.194 1.414 1.443
4 1.110 1.191 1.3014 1.1967 1.434 1.476
Mean 1.112 1.164 1.250 1.227 1.417 1.448
It is posited here that the model of motor unit syn-
chronicity during fatigue can be tested by determining the
dependence of the recorded signals. In order to confirm the
dependant properties of sources as explained in theory, a
Global matrix was computed.
The determinant of the global matrix is an indicator of the
dependence of the sources. If the sources are independent,
the determinant value is close to unity, whereas when there
is dependence between the sources, this value becomes close
to zero [15] .
• Independency Results (Before Fatigue: Beginning data)
G=
(
0.8418 −0.0100
−0.0755 1.0862
)
det(G) = 0.9135
• Dependency Results (Middle data)
G=
(
0.8763 0.0210
−0.6743 0.0130
)
det(G) = 0.0256
• Double dependency Results (After Fatigue: End data)
G=
(
0.0236 −0.0202
0.0057 0.0362
)
227211219219
0 0.5 1 1.5 2
x 105
−1.5
−1
−0.5
0
0.5
1
1.5
Two ChanneCyclic Fatigue data
0 0.5 1 1.5 2
x 105
−3
−2
−1
0
1
2
3
Beginning
data
Middle
data
Final stage
cyclic data
Figure 1. Plot showing the three SEMG subsets (beginning, middle and end) during cyclic contractions.
det(G) = 0.00096
Table IIDETERMINANT OF GLOBAL MATRIX FOR ICA SEPARATED SOURCES
FOR DIFFERENT ITERATIONS
Independency Dependency Double Dependency
0.9135 0.0256 0.00096
0.8905 0.0228 0.00090
0.9549 0.0231 0.00094
0.9015 0.0198 0.00089
0.8998 0.0267 0.00092
0.9106 0.0184 0.00088
0.9213 0.0229 0.00095
0.8978 0.0212 0.00091
0.9325 0.0205 0.00089
Mean = 0.9136 0.0223 0.00092
From Table II and Figure 3, it is observed that the
determinant of the global matrix for all subjects is close to
unity before fatigue and this moves closer to zero once the
subject becomes fatigued. This shows that when the muscle
is not fatigued, the motor units are firing independently and
when the muscle is fatigued, the motor units are dependant
and therefore more synchronized.
V. DISCUSSION AND CONCLUSION
Many research groups have reported a link between sEMG
spectrum (or median frequency) and fatigue. Fatigue has
been associated with a spectral shift towards lower frequen-
cies. However, it has been reported that that MF does not
change significantly with muscle fatigue at low contraction
levels [16]. Modeling studies have shown that unlike high
level of muscle contraction of the biceps, during low-level
bicep voluntary contractions, the motor unit conduction
velocity does not reduce. In the fatigue state, the central
drive to a muscle has to increase, leading to synaptic input
that is common to more than one neuron. This has been
explained in literature based on increased synchronicity in
the motor unit firing patterns.
From literature it is known that the human bicep muscle
recruits additional muscle fibers as force increases, up to
around 88% MVC. Above 88% MVC, the frequency of
motor unit firing increases to allow muscle force output to
modulate up to the maximal contraction force [17]. However,
both an increase in motor unit firing rate and an increase in
the number of active motor units can increase the signal
amplitude (measured by RMS of sEMG).
After the onset of muscle fatigue, increased effort is
required to sustain the same force level; a point which is
reflected in the uniform increase in RMS values. This paper
confirms these known results. However, this RMS increase
does not contribute to the practical knowledge regarding
motor unit synchronization.
The work presented here has tested the motor unit syn-
chronization model by associating synchronicity with de-
228212220220
1 2 3 41
1.1
1.2
1.3
1.4
1.5
CH
1− R
MS
1 2 3 41.1
1.2
1.3
1.4
1.5
Subjects
Ch
2− R
MS
Beginning During End
Figure 2. RMS of the separated sources for three subsets of cyclic data.
1 2 3 4 5 6 7 8 90
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8
0.9
1
Iterations
Det
erm
inan
t
Independency Dependency Double Dependency
Figure 3. Determinant values of global matrix for Independency, Dependency and Double dependency
pendence between motor units which are the sources of
MUAP. During non-fatigued state, the motor units appear
to work independently and this ensures smooth contraction.
SEMG taken from two channels should therefore reveal
independence from each other. This is confirmed from
the values of the determinants calculated using the global
matrix.
The determinant of the global matrix calculated after the
onset of muscle fatigue shows dependence between the two
channels. These results support the contention that motor
unit synchronicity increases in the fatigued state.
This work confirms the dependency between the differ-
ent channels. Work reported in this paper has determined
that determinant of the Global matrix associated with the
recordings can be used to determine the onset of muscle
fatigue even when the contraction is cyclic. This is important
because during cyclic contraction, it is difficult to obtain sta-
tionary features of sEMG that may be useful for determining
the onset of muscle fatigue.
The Global matrices showed a strong correlation between
fatigue and the matrix determinants. It is concluded by
this study that the correctness of the proposed motor unit
synchronization model to explain muscle fatigue. This paper
also reports that this fundamental property relating to muscle
229213221221
fatigue may be a used as an indicator for muscle fatigue.
However, the implementation of this would need to be
considered for real time applications.
ACKNOWLEDGMENT
The authors would like to acknowledge and thank Vivek
Yadav for collecting and providing the data for this research
study.
REFERENCES
[1] J. V. Basmajian and C. J. De Luca, Muscle Alive; TheirFunctions Revealed by Electromyography, The Williams &Wilkins Company Baltimore, 1929.
[2] S. Kumar and A. Mital, Electromyography in Ergonomics,Taylor and Francis, London, 1996.
[3] T. Moritani, M. Moro, and A. Nagata, ”Intramuscular andsurface electromyogram changes during muscle fatigue,” J AppPhysiol., vol. 60, pp. 1179-1185, 1986.
[4] G. Wang, X.-M. Reng, L. Li, and Z.-Z. Wang, ”Multifractalanalysis of surface EMG signals for assessing muscle fatigueduring static contractions,” Journal of Zhejiang University -Science A., vol. 8, pp. 910-915, 2007.
[5] G.M. Hagg, and J.R.M. Ojok, ”Isotonic and isoelectric en-durance tests for the upper trapezius muscle,” European Jour-nal of Applied Physiology, vol. 75, pp. 263-267, 1997.
[6] B.U. Kleine, D.F. Stegeman, D. Mund, and C. Anders, ”Influ-ence of motoneuron firing synchronization on SEMG charac-teristics in dependence of electrode position,” J Appl Physiol.,vol. 91, pp. 1588-1599, Oct. 2001.
[7] D.F. Stegeman, and W.H.J.P. Linssen, ”Muscle fiber actionpotential changes and surface EMG: A simulation study,” JEMG and Kinesiol., vol. 2, pp. 130-140, 1992.
[8] D. Farina, L. Fattorini, F. Felici, and G. Filligoi, ”Nonlinearsurface EMG analysis to detect changes of motor unit conduc-tion velocity and synchronization,” J Appl Physiol., vol. 93,pp. 1753-1763, Nov. 2002.
[9] G. R. Naik, D. K. Kumar, S. P. Arjunan, and K. Wheeler,”Testing of motor unit synchronization model for localizedmuscle fatigue,” Proceedings of IEEE-EMBS Conference, Sep.2009 (to be published).
[10] T. J. Dartnall, M. A. Nordstrom, and J. G. Semmler, ”Motorunit synchronization is increased in biceps bracii after exercise-induced damage to elbow flexor muscles,” J Neurophysiol., vol.99, pp. 1008-1019, Jan. 2008.
[11] P. Bonato, S. H. Roy, M. Knaflitz, and C. J. De Luca, ”Time-frequency parameters of the surface myoelectric signal forassessing muscle fatigue during cyclic dynamic contractions,”IEEE Transactions on Biomedical Engineering, vol. 48, pp.745-753, July. 2001.
[12] G.R. Naik, D.K. Kumar, and H. Weghorn, ”ICA based identi-fication of sources in sEMG,” IEEE 3rd International Confer-ence on Intelligent Sensors, Sensor Networks and Information(ISSNIP 2007), Melbourne, Australia, 2007, pp. 619-624.
[13] G.R. Naik, D.K. Kumar, and M. Palaniswami, ”Classificationof Surface Electromyogram for Prosthetics Control,” IET sig-nal processing (previously IEE) Journal, UK, Accepted, 2008.
[14] A. Cichocki, and S. Amari, Adaptive Blind Signal and ImageProcessing, New York: John Wiley, 2002.
[15] C. D. Meyer, Matrix Analysis and Applied Linear Algebra,UK:Cambridge, 2000.
[16] T. Oberg, L. Sandsjo, and R. Kadefors, ”Subjective andobjective evaluation of shoulder muscle fatigue,” Ergonomics,vol. 37, pp. 1323-1333, 1994.
[17] C.G. Kukulka, and H.P. Clamann, ”Comparison of the recruit-ment and discharge properties of motor units in human brachialbiceps and adductor pollicis during isometric contractions,”Brain Research, vol. 219, pp. 45-55, 1981.
230214222222