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International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056
Volume: 06 Issue: 08 | Aug 2019 www.irjet.net p-ISSN: 2395-0072
© 2019, IRJET | Impact Factor value: 7.34 | ISO 9001:2008 Certified Journal | Page 1252
Analysis of Epilepsy using Approximate Entropy Algorithm
Vallabh Budhkar1, Sanskruta Dhotre2, Dr. Saurav Mitra3
1Former Student, Department of Electronics Engineering, Vidyalankar Institute of Technology.
2Former Student, Department of Electronics Engineering, Vidyalankar Institute of Technology.
3Professor, Department of Electronics and Communication Engineering, KLS Gogte Institute of Technology.
---------------------------------------------------------------------***----------------------------------------------------------------------
Abstract – Degree of anomaly in EEG based brainwave
signal picked up during seizure is found to be most severe.
There are various methods of detecting epilepsy in patients.
The algorithm used here for detection of epilepsy is called
Approximate Entropy (ApEn). This algorithm helps to identify
irregularity and unpredictabilityin EEGsignal. Our workgives
ApEn based measure for the anomalous characteristicpresent
in the EEG brain waves. The proposedcriticalandquantitative
analysis clearly distinguishes between EEG waves of epileptic
and non-epileptic subjects.
Key Words: EEG, Epilepsy, Approximate Entropy (ApEn)
1. INTRODUCTION
Brainwaves are the rhythmic neural activity found in
human nervous system. This activity is measured by the
diagnostic process called electroencephalography (EEG).
EEG signals are also used for analysis and identification of
cerebral diseases in patients. Epilepsy occurs mainly due to
irregularity in human brain activities. Though small
percentage of people in societysuffersfromit, butifdetected
at early age, it may be cured. Epilepsy causes frequent
seizures in patients. Abnormal variations in EEG frequency
bear sign of epilepsy in the patient. The ApEn algorithm is
apt for detection of epilepsy, probably present in a person.
ApEn algorithm fulfils the objective of epilepsy detection in
our case.
ApEn is a time-based function and helps measure the
unpredictability and irregularity in EEG signal [1]. ApEn can
classify complex systems even when the system contains
deterministic, chaotic and stochastic process in it [2]. The
other methods for analyzing epileptic signals from EEG are
Discrete Wavelet Transform (DWT), Lomb-Scargle
Periodogram, Cosine SimilarityMeasure, etc.Thesemethods
are based on calculation of the energy which may not result
in accurate detection, since high signal energy is not always
the distinguishing characteristic for epileptic signals.
EEG measures neural oscillations that occur as a result of
the voltage fluctuations due to ionic (Na+ & K+) discharges
of the brain neurons [3]. The neurons pass information
through the process of discharging and accepting these ions
through synapses. This electrical activity generates
brainwaves. EEG is non-invasive method of measuring
brainwaves. There are invasive methods also for measuring
brain activity called as electrocorticography.
Alaa Eldeen MahmoudHelal et. al. proposedLomb-Scargle
Periodogram and Cosine Similarity Measure together to
detect the probable existence of epileptic natured signal in
EEG [4]. The Lomb-Scargle Periodogram was used to
measure instantaneous increase in the energy of an EEG
waveform. The power spectrumofthesignal wasconsidered
in this case. The Cosine Similarity Measure was used to
measure the cosine of the angle between a normal and an
elliptic EEG wave. This similarity measure is mainly usedfor
high dimension positive spaces. Tiny changes were
observed in the angle by precise increment or decrement in
its cosine value in case of two dissimilar waves.
Kamath and Chandrakar proposed two quantifiers from
nonlinear dynamics and chaos theory. The qualifiers were
Central tendency measure (CTM) and Higuchi fractal
dimension (HFD) [5]. CTM was used to quantify the degree
of variability and HFD was used toquantifycomplexityofthe
signals [5].
2. OVERVIEW
Epilepsy is a type of neurological disorder whichresultsin
seizures. The EEG based recordings of epileptic events are
characterized by spike and wave patterns. ApEn algorithm
analyses these wave patterns and displays output regarding
presence of epileptic trend in patient. For any brainwave
picked up through the EEG electrodes, corresponding
numeric ApEn value may be deduced. The spike and wave
patterns occur due to the repolarization and depolarization
of the ionic sodium and potassium channels in human brain.
Proper and timely diagnosis of epileptic trend in a patient
helps to control the disease with medication. Though
epilepsy and related seizure does not kill a patient directly,
but the trauma and accidents caused during the seizuremay
be life threatening. Through prolonged medication, the
severity of seizure and fatality in a patient can be controlled.
ApproximateEntropyalgorithmuseslargeamountofdata.
ApEn is an offline process and with good computational
facilities, it can accurately analyze probableepileptictrendin
a patient. The results are also subject to the accuracy of the
experimental conditions during the state of recording. Our
work offers a unique approachusingApEnleadingtotheease
of qualitative detection of epilepsy in a patient.
The standard traditional methods involving mean and
variance do not giveaccurateresultswhenthevolumeofdata
set and the number of data points increases. In such cases,
Approximate Entropy provides far more efficiency. Hence,
ApEn is a far better method than DWT for analyzing big EEG
International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056
Volume: 06 Issue: 08 | Aug 2019 www.irjet.net p-ISSN: 2395-0072
© 2019, IRJET | Impact Factor value: 7.34 | ISO 9001:2008 Certified Journal | Page 1253
data sets. The main contribution of this work is development
of proper ApEn algorithm and to logically decide the
threshold value for detection of epileptic trend in a patient.
The analysis also proves that this method is more efficient
due to its ease of detection and high diagnostic accuracy.
3. METHODOLOGY
In this section, various steps of ApEn algorithm are
detailed. The test data set is same as mentioned in the
research paper of Andrzejak et. al. [6]. The data set
comprises EEG data of four subjects in normal state as well
as during seizures [6]. Seizure data is available only for
epileptic patients. For every patient, EEG data is collected
over 100 single channels. Each of the recorded 100 channel
continuous EEG data stream is first sampled using sampling
frequency of 173.61 Hz. Each sampled data stream is cut for
23.6 second long sequences that comprise 4097 points [3].
The EEG signals of two non epileptic and two epileptic
subjects are considered here under certain pre defined
medical test conditions. The four test conditions are
A] Normally relaxed eyes closed
B] Normally relaxed eyes open
C] Non-seizure (epileptogenic region) - invasive
D] During seizures (for epileptic patients only)
Among the 4 conditions mentioned above, condition C is
invasive whereas A, B and D are non-invasive type [4]. The
first two subjects (sub1 and sub 2) are non-epileptic. For
these two subjects, EEG data are recorded forconditionsA,B
and C, whereas for the epileptic subjects 3 and 4, EEG data
for all four conditions (A to D) are recorded. These facts are
tabulated in Table 1. For each patient, for each condition, at
first, 100 data streams of 23.6 seconds duration each are
generated. Then ApEn value is calculated for each of these
100 segments. Finally, for each patient, for each condition,
the calculated 100 ApEn values areplottedinonegraph with
x axis being the integer value of the data segment. This data
segment value ranges from 1 to100. Finally, integration of
this ApEn plot gives us the ‘unified ApEn value’ for that
subject for that particular condition. The steps of this
particular algorithmandthe relatedmathematical treatment
are given below in this section itself.
Table -1: Subject Type and Data Set for ApEn Plots
Sub.
No.
Subject
Type
Test Conditions
A B C D
Sub. 1 Non-Epileptic √ √ √ NA
Sub. 2 Non-Epileptic √ √ √ NA
Sub. 3 Epileptic √ √ √ √
Sub. 4 Epileptic √ √ √ √
The Approximate Entropy algorithm actually an anomaly
measure of the EEG brainwave signal. It is a time-based
function which provideswitha singlevaluecorrespondingto
the number of similar patterns observed in the signal. The
mathematics behind our ApEn algorithm is as follows: Fig-1: Flowchart of the ApEn algorithm pressented here
International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056
Volume: 06 Issue: 08 | Aug 2019 www.irjet.net p-ISSN: 2395-0072
© 2019, IRJET | Impact Factor value: 7.34 | ISO 9001:2008 Certified Journal | Page 1254
Step 1: The recorded signal is stored in the form of a matrix
‘W’. Matrix ‘W’ contains ‘n’ number of points. In this case n=
4097. This raw data is measured after equal periods of time.
Step 2: Let ‘m’ be a value for the length of subsequence
matrix. ‘m’ is any positive integer. ‘r’ is the level of the noise
filter. Value of r = (0.1*standard deviation of ‘W’ matrix)
Step 3: Let ‘X’ be a subsequence vector matrix of ‘W’ such
that,
[1] { [1], [2]}
[2] { [2], [3]}
[3] { [3], [4]}
.
.
.
.
[ 1] { [ 1], [ ]}
x w w
x w w
x w w
x n m w n w n



   
(1)
Step 4: Compare ( )w i with ( )w j to find the distance
between vectors ( )w i and ( )w j .
[ ( ), ( )] max ( ) ( )d x i x j w i w j  , (2)
where 1,k  1 [ ( ), ( )]d x i x j n m  
and 0,k  otherwise
Step 5: Using the above vector sequence we construct,
( )m
ic r Number of x(j) such that
[ ( ), ( ]) /( 1)d x i x j r n m   (3)
This function basically computes the average of all the
distances that satisfies step 4. In equation (2), ( )w i and
( )w j are scalar values whereas [ ( ), ( ])d x i x j is the
distance between the vectors.
Step 6: The ( )m
r correlation is calculated next
1
1
1
( ) ( 1) log( ( ))
n m
m m
i
i
r n m c r
 


    (4)
Step 7: Repeat now the steps 2 to step 6 for 1m m 
Step 8: As a result of Step 7 we will get
1
( )m
r 
1
1 1
1
( ) ( 1) log( ( ))
n m
m m
i
i
r n m c r
 
 

    (5)
Step 9: Approximate Entropy ApEn in next defined as,
1
( ) ( )m m
ApEn r r  
  (6)
Approximate Entropy is widely used for the analysis of
large EEG data especially in the cases of neuro-physical
diseases such as epilepsy,schizophrenia,addiction, etc. Fig2,
shown at the top of the right-side column in this page
illustrates that maximum value of ApEn wouldindicatemost
complex signal [7]. So, white noise has highest complexity
followed by chirp and then sine wave signal.
Fig-2: Average figure of the approximate entropy ApEn
value for Sine, Chirp, and White noise inputs [7]
4. RESULTS AND DISCUSSION
The ApEn analysis is performed on the EEG signals picked
up from four different subjects. Each set of EEG contains 100
channel continuous time brainwave signals. Thenthesignals
are sampledanddiscretedatasequencesareproduced.These
sequences are used in ApEn algorithm.
For two non-epileptic subjects, EEG data are picked up for
conditions A, B and C each as mentioned in Table 1. Hence,
there are total 6 data sets picked up from non-epileptic
subjects. For epilepticsubjects, EEG dataare picked upforall
four conditions, Table 1. It means, forepileptic subjects, total
8 sets of data can be obtained. Totally there are 14 data sets
on which ApEn algorithm can be tested. But, for ease of
demonstration under this section, we have taken only four
judiciously chosen data sets. Epilepsy detection inference is
drawn from these four data sets after ApEn based analysis.
The four EEG data sets with darker and bigger tick marks
(√) in Table 1 are those data sets for which integrated ApEn
waveform are generated. The integrated ApEn waveforms
obtained for these four chosen sets of EEG data which are
picked up from four different subjects under four different
medical test conditions are analyzed here in this section. For
non-epileptic subject 1, EEG data set of condition A is
considered. This is the ‘Normally relaxed eyes closed’
condition. Next, foranother non-epileptic subject2,EEGdata
set with condition B is considered. This is ‘Normally relaxed
eyes open’ condition. These two integrated ApEn waves are
shown in figure 3 and figure4 respectively.Next,forsubject3
who is an epileptic subject, EEG data is invasively picked up
from the epileptogenic region of the brain under normally
relaxed condition. Finally, forthe 4th subject who is epileptic,
EEG data are picked up non-invasively during seizure. The
integrated ApEn wave generated for subject 3 and subject 4
are shown in figure 5 and figure 6 respectively. From design
of experiment point of view, it can be observed that the
degree of stimuli applied to the subjectsisincreasedfromthe
first to the fourth data set.
International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056
Volume: 06 Issue: 08 | Aug 2019 www.irjet.net p-ISSN: 2395-0072
© 2019, IRJET | Impact Factor value: 7.34 | ISO 9001:2008 Certified Journal | Page 1255
Fig-3: Integrated ApEn waveform for 100 channels EEG
segments for non-epileptic subject 1, with closed eyes
A. Non Epileptic Subject 1 – Relaxed & Eyes Closed
This is the first integrated ApEnwaveformgeneratedfora
non-epileptic subject under completely relaxed condition.
The eyes of the subject were also closed during EEG
recording. Hence, very less or no external stimuli were
administered to the subject. The integrated ApEn waveform
is shown in figure 3 above. The integrated ApEnwaveshows
minimal variation and hence the overall ApEn value of the
signal is lowest amongst all four sets of observed data. The
count 1 to 100 in the x-axis indicates the 100channelswhich
are used for EEG wave pick up. For this reason, no reading is
registered for the value 0 in any of the graphs.
Fig-4: Integrated ApEn waveform for 100 channels EEG
segments for non-epileptic subject 2, with open eyes
B. Non Epileptic Subject 2 – Relaxed & Eyes Opened
This is the second integrated ApEn waveform generated
for a non-epileptic subject under completely relaxed
condition, figure 4. The eyes of the subject were open during
recording of the EEG signal in this case. Open eyes indicate
Fig-5: Integrated ApEn wave for relaxed epileptic subject
3, EEG picked up invasively from epileptogenic brain
region
presence of little amount of natural stimuli during EEG
recording. For non-epileptic subjects,randomvariations are
generally not present in EEG waveforms because these
subjects do not have seizures. But due to presence of optical
stimuli, the ApEn wave of figure 4, is found to have more
random variation than that of figure 3. For the same reason,
the integrated ApEn value for the wave in figure 4 is higher
than that shown in figure 3.
C. Epileptic Subject 3-Epileptogenic Zone, Nonseizure
Figure 5 above shows the integrated ApEn wave for 100
channel EEG waveforms picked up for an epileptic subject.
EEG electrodes were invasively placed in the intracranial
epileptogenic brain region while EEG recording. The subject
was in relaxed condition with opened eyes. Though the
patient is epileptic, during the EEGrecordingthesubject was
not having seizure. The integrated ApEn value for epileptic
subject 3 is higher than that of non-epileptic subject 2.
Fig-6: Integrated ApEn wave for epileptic subject 4, 100
channel EEG picked up noninvasively during seizure
International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056
Volume: 06 Issue: 08 | Aug 2019 www.irjet.net p-ISSN: 2395-0072
© 2019, IRJET | Impact Factor value: 7.34 | ISO 9001:2008 Certified Journal | Page 1256
D. Epileptic Subject 4 – EEG During Seizure
Figure 6, shown toward the end of previous page shows
the integrated ApEn wave for 100 channel noninvasive EEG
signals picked up for an epileptic subject during seizure –
subject 4. Normal EEG for epileptic subjects shows more
random variations than that of non-epileptic subjects. For
epileptic subject EEG when the effect of occurring seizure
gets added, it results huge amount of random variations in
EEG waveforms. The same is depictedintheintegratedApEn
waveforms for subject 4, as shown in fig. 6. The integrated
ApEn value here is largest among all 4 cases shown in Table
2. It indicates huge amount of variations in EEG wave which
is caused by seizure in epileptic patients.
Table -2: Estimated integrated ApEn values obtained
for all four subjects under four different test conditions
Sr.
No.
Medical Test
Condition
Integrated
ApEn Value
Inference
1.
Non-epileptic
eyes closed (A)
2.7259 Lowest ApEn Value
2.
Non-epileptic
eyes open (B)
2.8384 Low ApEn Value
3.
Epileptic
relaxed (C)
3.4372 Higher ApEn Value
4.
Epileptic in
seizure (D)
3.4902 Highest ApEn Value
5. CONCLUSIONS AND FUTURE SCOPE
The estimated integrated ApEn values shown in Table 2
are for the four different medical test conditions which are
mentioned in Table 1. For the medical test condition A, for a
relaxed non-epileptic subject with closed eyes, integrated
ApEn value is 2.7259. This is lowest integrated ApEn value
among all four test conditions. It indicates that for that test
condition where the subject is healthy and is without any
external stimuli, integrated ApEn valuewouldbelowest.It is
because the random variations in this waveform areleast. In
the next case, for test condition B where the non-epileptic
subject has kept his eyes open during EEG pick up,
integrated ApEn value has increased little to 2.8384. This
slight increment is the result of the optical stimuli
administered to the subject during EEG process. In the next
case for test condition C which considers anepilepticsubject
in relaxed state, integrated ApEn value suddenly jumps to
3.4372. This value is considerably higher than that found in
under test condition B for non-epileptic subject. Finally,
highest degree of randomness and highest ApEn value is
estimated for the subject 4 under test condition D where
integrated wave is recorded during seizure for an epileptic
subject. Table 2 shows ascending order of integrated ApEn
values for ascending degree of randomnessinpickedupEEG
signal.
This work presents a unique method for extraction of
relevant information from noisy EEG signals. This work also
explains the related signal classification algorithm.
Approximate Entropy is an algorithm used for fulfilling our
objective. Approximate Entropy is the time-based function
which measures the irregularity and randomness in EEG
signal. The algorithm delivers a single value at the end of
processing every data set. From the graphs showninfigure3
to figure 6 above, we can conclude that increase in value of
ApEn indicates higher degree of randomness in EEG wave
which in turn indicate presence of higher epileptic signal
component in EEG signal. Thus, we can conclude that as the
severity of epilepsy increases (from non-epileptic person to
an epileptic person) the ApEn value also increases.
The analysis of epilepsy can be further improved if
machine learningalgorithms areappliedtotherecordedEEG
signals under different medical test conditions. More data
can be fed to the system to enhance the learningcapability of
the system. More precise decision making is possible
through enhancement in signal processing algorithms.
Machine learning helps in better pattern recognition which
in turn helps to achieve higher estimation accuracy.
REFERENCES
[1] Srinivasan, Vairavan, Chikkannan Eswaran, and
Natarajan Sriraam, "Approximate entropy-based
epileptic EEG detectionusing artificial neural networks,"
IEEE Transactions on information Technology in
Biomedicine, vol. 11, no. 3, (2007): 288-295.
[2] Pincus, Steven M. "Approximate entropyasa measureof
system complexity," Proceedings of the National
Academy of Sciences 88, no. 6 (1991): 2297-2301.
[3] M. Teplan, “Fundamentals of EEG Measurement,”
Institute of Measurement Science, Slovak Academy of
Sciences, Dúbravská cesta 9841 04 Bratislava, Slovakia.
[4] Helal, Alaa Eldeen Mahmoud, Ahmed Farag Seddik,
Mohammed Ali Eldosoky, and Ayat Allah Farouk
Hussein. "An Efficient Method for Epileptic Seizure
Detection in Long-Term EEG Recordings," Journal of
Biomedical Science and Engineering 7, no. 12 (2014):
963.
[5] Kamath, Chandrakar. (2015).”Analysis of EEG signals in
epileptic patients and control subjects using nonlinear
deterministic chaotic and fractal quantifiers,” Science
Postprint. 1. 10.14340/spp.2015.01A0003.
[6] Andrzejak, Ralph G., Klaus Lehnertz, Florian Mormann,
Christoph Rieke, Peter David, and Christian E. Elger.
"Indications of nonlinear deterministic and finite-
dimensional structures in time series of brain electrical
activity: Dependence on recording region and brain
state," Physical Review E 64, no. 6 (2001): 061907.
[7] https://www.mathworks.com/matlabcentral/fileexchan
ge/32427-fast-approximate-entropy

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IRJET- Analysis of Epilepsy using Approximate Entropy Algorithm

  • 1. International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056 Volume: 06 Issue: 08 | Aug 2019 www.irjet.net p-ISSN: 2395-0072 © 2019, IRJET | Impact Factor value: 7.34 | ISO 9001:2008 Certified Journal | Page 1252 Analysis of Epilepsy using Approximate Entropy Algorithm Vallabh Budhkar1, Sanskruta Dhotre2, Dr. Saurav Mitra3 1Former Student, Department of Electronics Engineering, Vidyalankar Institute of Technology. 2Former Student, Department of Electronics Engineering, Vidyalankar Institute of Technology. 3Professor, Department of Electronics and Communication Engineering, KLS Gogte Institute of Technology. ---------------------------------------------------------------------***---------------------------------------------------------------------- Abstract – Degree of anomaly in EEG based brainwave signal picked up during seizure is found to be most severe. There are various methods of detecting epilepsy in patients. The algorithm used here for detection of epilepsy is called Approximate Entropy (ApEn). This algorithm helps to identify irregularity and unpredictabilityin EEGsignal. Our workgives ApEn based measure for the anomalous characteristicpresent in the EEG brain waves. The proposedcriticalandquantitative analysis clearly distinguishes between EEG waves of epileptic and non-epileptic subjects. Key Words: EEG, Epilepsy, Approximate Entropy (ApEn) 1. INTRODUCTION Brainwaves are the rhythmic neural activity found in human nervous system. This activity is measured by the diagnostic process called electroencephalography (EEG). EEG signals are also used for analysis and identification of cerebral diseases in patients. Epilepsy occurs mainly due to irregularity in human brain activities. Though small percentage of people in societysuffersfromit, butifdetected at early age, it may be cured. Epilepsy causes frequent seizures in patients. Abnormal variations in EEG frequency bear sign of epilepsy in the patient. The ApEn algorithm is apt for detection of epilepsy, probably present in a person. ApEn algorithm fulfils the objective of epilepsy detection in our case. ApEn is a time-based function and helps measure the unpredictability and irregularity in EEG signal [1]. ApEn can classify complex systems even when the system contains deterministic, chaotic and stochastic process in it [2]. The other methods for analyzing epileptic signals from EEG are Discrete Wavelet Transform (DWT), Lomb-Scargle Periodogram, Cosine SimilarityMeasure, etc.Thesemethods are based on calculation of the energy which may not result in accurate detection, since high signal energy is not always the distinguishing characteristic for epileptic signals. EEG measures neural oscillations that occur as a result of the voltage fluctuations due to ionic (Na+ & K+) discharges of the brain neurons [3]. The neurons pass information through the process of discharging and accepting these ions through synapses. This electrical activity generates brainwaves. EEG is non-invasive method of measuring brainwaves. There are invasive methods also for measuring brain activity called as electrocorticography. Alaa Eldeen MahmoudHelal et. al. proposedLomb-Scargle Periodogram and Cosine Similarity Measure together to detect the probable existence of epileptic natured signal in EEG [4]. The Lomb-Scargle Periodogram was used to measure instantaneous increase in the energy of an EEG waveform. The power spectrumofthesignal wasconsidered in this case. The Cosine Similarity Measure was used to measure the cosine of the angle between a normal and an elliptic EEG wave. This similarity measure is mainly usedfor high dimension positive spaces. Tiny changes were observed in the angle by precise increment or decrement in its cosine value in case of two dissimilar waves. Kamath and Chandrakar proposed two quantifiers from nonlinear dynamics and chaos theory. The qualifiers were Central tendency measure (CTM) and Higuchi fractal dimension (HFD) [5]. CTM was used to quantify the degree of variability and HFD was used toquantifycomplexityofthe signals [5]. 2. OVERVIEW Epilepsy is a type of neurological disorder whichresultsin seizures. The EEG based recordings of epileptic events are characterized by spike and wave patterns. ApEn algorithm analyses these wave patterns and displays output regarding presence of epileptic trend in patient. For any brainwave picked up through the EEG electrodes, corresponding numeric ApEn value may be deduced. The spike and wave patterns occur due to the repolarization and depolarization of the ionic sodium and potassium channels in human brain. Proper and timely diagnosis of epileptic trend in a patient helps to control the disease with medication. Though epilepsy and related seizure does not kill a patient directly, but the trauma and accidents caused during the seizuremay be life threatening. Through prolonged medication, the severity of seizure and fatality in a patient can be controlled. ApproximateEntropyalgorithmuseslargeamountofdata. ApEn is an offline process and with good computational facilities, it can accurately analyze probableepileptictrendin a patient. The results are also subject to the accuracy of the experimental conditions during the state of recording. Our work offers a unique approachusingApEnleadingtotheease of qualitative detection of epilepsy in a patient. The standard traditional methods involving mean and variance do not giveaccurateresultswhenthevolumeofdata set and the number of data points increases. In such cases, Approximate Entropy provides far more efficiency. Hence, ApEn is a far better method than DWT for analyzing big EEG
  • 2. International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056 Volume: 06 Issue: 08 | Aug 2019 www.irjet.net p-ISSN: 2395-0072 © 2019, IRJET | Impact Factor value: 7.34 | ISO 9001:2008 Certified Journal | Page 1253 data sets. The main contribution of this work is development of proper ApEn algorithm and to logically decide the threshold value for detection of epileptic trend in a patient. The analysis also proves that this method is more efficient due to its ease of detection and high diagnostic accuracy. 3. METHODOLOGY In this section, various steps of ApEn algorithm are detailed. The test data set is same as mentioned in the research paper of Andrzejak et. al. [6]. The data set comprises EEG data of four subjects in normal state as well as during seizures [6]. Seizure data is available only for epileptic patients. For every patient, EEG data is collected over 100 single channels. Each of the recorded 100 channel continuous EEG data stream is first sampled using sampling frequency of 173.61 Hz. Each sampled data stream is cut for 23.6 second long sequences that comprise 4097 points [3]. The EEG signals of two non epileptic and two epileptic subjects are considered here under certain pre defined medical test conditions. The four test conditions are A] Normally relaxed eyes closed B] Normally relaxed eyes open C] Non-seizure (epileptogenic region) - invasive D] During seizures (for epileptic patients only) Among the 4 conditions mentioned above, condition C is invasive whereas A, B and D are non-invasive type [4]. The first two subjects (sub1 and sub 2) are non-epileptic. For these two subjects, EEG data are recorded forconditionsA,B and C, whereas for the epileptic subjects 3 and 4, EEG data for all four conditions (A to D) are recorded. These facts are tabulated in Table 1. For each patient, for each condition, at first, 100 data streams of 23.6 seconds duration each are generated. Then ApEn value is calculated for each of these 100 segments. Finally, for each patient, for each condition, the calculated 100 ApEn values areplottedinonegraph with x axis being the integer value of the data segment. This data segment value ranges from 1 to100. Finally, integration of this ApEn plot gives us the ‘unified ApEn value’ for that subject for that particular condition. The steps of this particular algorithmandthe relatedmathematical treatment are given below in this section itself. Table -1: Subject Type and Data Set for ApEn Plots Sub. No. Subject Type Test Conditions A B C D Sub. 1 Non-Epileptic √ √ √ NA Sub. 2 Non-Epileptic √ √ √ NA Sub. 3 Epileptic √ √ √ √ Sub. 4 Epileptic √ √ √ √ The Approximate Entropy algorithm actually an anomaly measure of the EEG brainwave signal. It is a time-based function which provideswitha singlevaluecorrespondingto the number of similar patterns observed in the signal. The mathematics behind our ApEn algorithm is as follows: Fig-1: Flowchart of the ApEn algorithm pressented here
  • 3. International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056 Volume: 06 Issue: 08 | Aug 2019 www.irjet.net p-ISSN: 2395-0072 © 2019, IRJET | Impact Factor value: 7.34 | ISO 9001:2008 Certified Journal | Page 1254 Step 1: The recorded signal is stored in the form of a matrix ‘W’. Matrix ‘W’ contains ‘n’ number of points. In this case n= 4097. This raw data is measured after equal periods of time. Step 2: Let ‘m’ be a value for the length of subsequence matrix. ‘m’ is any positive integer. ‘r’ is the level of the noise filter. Value of r = (0.1*standard deviation of ‘W’ matrix) Step 3: Let ‘X’ be a subsequence vector matrix of ‘W’ such that, [1] { [1], [2]} [2] { [2], [3]} [3] { [3], [4]} . . . . [ 1] { [ 1], [ ]} x w w x w w x w w x n m w n w n        (1) Step 4: Compare ( )w i with ( )w j to find the distance between vectors ( )w i and ( )w j . [ ( ), ( )] max ( ) ( )d x i x j w i w j  , (2) where 1,k  1 [ ( ), ( )]d x i x j n m   and 0,k  otherwise Step 5: Using the above vector sequence we construct, ( )m ic r Number of x(j) such that [ ( ), ( ]) /( 1)d x i x j r n m   (3) This function basically computes the average of all the distances that satisfies step 4. In equation (2), ( )w i and ( )w j are scalar values whereas [ ( ), ( ])d x i x j is the distance between the vectors. Step 6: The ( )m r correlation is calculated next 1 1 1 ( ) ( 1) log( ( )) n m m m i i r n m c r         (4) Step 7: Repeat now the steps 2 to step 6 for 1m m  Step 8: As a result of Step 7 we will get 1 ( )m r  1 1 1 1 ( ) ( 1) log( ( )) n m m m i i r n m c r          (5) Step 9: Approximate Entropy ApEn in next defined as, 1 ( ) ( )m m ApEn r r     (6) Approximate Entropy is widely used for the analysis of large EEG data especially in the cases of neuro-physical diseases such as epilepsy,schizophrenia,addiction, etc. Fig2, shown at the top of the right-side column in this page illustrates that maximum value of ApEn wouldindicatemost complex signal [7]. So, white noise has highest complexity followed by chirp and then sine wave signal. Fig-2: Average figure of the approximate entropy ApEn value for Sine, Chirp, and White noise inputs [7] 4. RESULTS AND DISCUSSION The ApEn analysis is performed on the EEG signals picked up from four different subjects. Each set of EEG contains 100 channel continuous time brainwave signals. Thenthesignals are sampledanddiscretedatasequencesareproduced.These sequences are used in ApEn algorithm. For two non-epileptic subjects, EEG data are picked up for conditions A, B and C each as mentioned in Table 1. Hence, there are total 6 data sets picked up from non-epileptic subjects. For epilepticsubjects, EEG dataare picked upforall four conditions, Table 1. It means, forepileptic subjects, total 8 sets of data can be obtained. Totally there are 14 data sets on which ApEn algorithm can be tested. But, for ease of demonstration under this section, we have taken only four judiciously chosen data sets. Epilepsy detection inference is drawn from these four data sets after ApEn based analysis. The four EEG data sets with darker and bigger tick marks (√) in Table 1 are those data sets for which integrated ApEn waveform are generated. The integrated ApEn waveforms obtained for these four chosen sets of EEG data which are picked up from four different subjects under four different medical test conditions are analyzed here in this section. For non-epileptic subject 1, EEG data set of condition A is considered. This is the ‘Normally relaxed eyes closed’ condition. Next, foranother non-epileptic subject2,EEGdata set with condition B is considered. This is ‘Normally relaxed eyes open’ condition. These two integrated ApEn waves are shown in figure 3 and figure4 respectively.Next,forsubject3 who is an epileptic subject, EEG data is invasively picked up from the epileptogenic region of the brain under normally relaxed condition. Finally, forthe 4th subject who is epileptic, EEG data are picked up non-invasively during seizure. The integrated ApEn wave generated for subject 3 and subject 4 are shown in figure 5 and figure 6 respectively. From design of experiment point of view, it can be observed that the degree of stimuli applied to the subjectsisincreasedfromthe first to the fourth data set.
  • 4. International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056 Volume: 06 Issue: 08 | Aug 2019 www.irjet.net p-ISSN: 2395-0072 © 2019, IRJET | Impact Factor value: 7.34 | ISO 9001:2008 Certified Journal | Page 1255 Fig-3: Integrated ApEn waveform for 100 channels EEG segments for non-epileptic subject 1, with closed eyes A. Non Epileptic Subject 1 – Relaxed & Eyes Closed This is the first integrated ApEnwaveformgeneratedfora non-epileptic subject under completely relaxed condition. The eyes of the subject were also closed during EEG recording. Hence, very less or no external stimuli were administered to the subject. The integrated ApEn waveform is shown in figure 3 above. The integrated ApEnwaveshows minimal variation and hence the overall ApEn value of the signal is lowest amongst all four sets of observed data. The count 1 to 100 in the x-axis indicates the 100channelswhich are used for EEG wave pick up. For this reason, no reading is registered for the value 0 in any of the graphs. Fig-4: Integrated ApEn waveform for 100 channels EEG segments for non-epileptic subject 2, with open eyes B. Non Epileptic Subject 2 – Relaxed & Eyes Opened This is the second integrated ApEn waveform generated for a non-epileptic subject under completely relaxed condition, figure 4. The eyes of the subject were open during recording of the EEG signal in this case. Open eyes indicate Fig-5: Integrated ApEn wave for relaxed epileptic subject 3, EEG picked up invasively from epileptogenic brain region presence of little amount of natural stimuli during EEG recording. For non-epileptic subjects,randomvariations are generally not present in EEG waveforms because these subjects do not have seizures. But due to presence of optical stimuli, the ApEn wave of figure 4, is found to have more random variation than that of figure 3. For the same reason, the integrated ApEn value for the wave in figure 4 is higher than that shown in figure 3. C. Epileptic Subject 3-Epileptogenic Zone, Nonseizure Figure 5 above shows the integrated ApEn wave for 100 channel EEG waveforms picked up for an epileptic subject. EEG electrodes were invasively placed in the intracranial epileptogenic brain region while EEG recording. The subject was in relaxed condition with opened eyes. Though the patient is epileptic, during the EEGrecordingthesubject was not having seizure. The integrated ApEn value for epileptic subject 3 is higher than that of non-epileptic subject 2. Fig-6: Integrated ApEn wave for epileptic subject 4, 100 channel EEG picked up noninvasively during seizure
  • 5. International Research Journal of Engineering and Technology (IRJET) e-ISSN: 2395-0056 Volume: 06 Issue: 08 | Aug 2019 www.irjet.net p-ISSN: 2395-0072 © 2019, IRJET | Impact Factor value: 7.34 | ISO 9001:2008 Certified Journal | Page 1256 D. Epileptic Subject 4 – EEG During Seizure Figure 6, shown toward the end of previous page shows the integrated ApEn wave for 100 channel noninvasive EEG signals picked up for an epileptic subject during seizure – subject 4. Normal EEG for epileptic subjects shows more random variations than that of non-epileptic subjects. For epileptic subject EEG when the effect of occurring seizure gets added, it results huge amount of random variations in EEG waveforms. The same is depictedintheintegratedApEn waveforms for subject 4, as shown in fig. 6. The integrated ApEn value here is largest among all 4 cases shown in Table 2. It indicates huge amount of variations in EEG wave which is caused by seizure in epileptic patients. Table -2: Estimated integrated ApEn values obtained for all four subjects under four different test conditions Sr. No. Medical Test Condition Integrated ApEn Value Inference 1. Non-epileptic eyes closed (A) 2.7259 Lowest ApEn Value 2. Non-epileptic eyes open (B) 2.8384 Low ApEn Value 3. Epileptic relaxed (C) 3.4372 Higher ApEn Value 4. Epileptic in seizure (D) 3.4902 Highest ApEn Value 5. CONCLUSIONS AND FUTURE SCOPE The estimated integrated ApEn values shown in Table 2 are for the four different medical test conditions which are mentioned in Table 1. For the medical test condition A, for a relaxed non-epileptic subject with closed eyes, integrated ApEn value is 2.7259. This is lowest integrated ApEn value among all four test conditions. It indicates that for that test condition where the subject is healthy and is without any external stimuli, integrated ApEn valuewouldbelowest.It is because the random variations in this waveform areleast. In the next case, for test condition B where the non-epileptic subject has kept his eyes open during EEG pick up, integrated ApEn value has increased little to 2.8384. This slight increment is the result of the optical stimuli administered to the subject during EEG process. In the next case for test condition C which considers anepilepticsubject in relaxed state, integrated ApEn value suddenly jumps to 3.4372. This value is considerably higher than that found in under test condition B for non-epileptic subject. Finally, highest degree of randomness and highest ApEn value is estimated for the subject 4 under test condition D where integrated wave is recorded during seizure for an epileptic subject. Table 2 shows ascending order of integrated ApEn values for ascending degree of randomnessinpickedupEEG signal. This work presents a unique method for extraction of relevant information from noisy EEG signals. This work also explains the related signal classification algorithm. Approximate Entropy is an algorithm used for fulfilling our objective. Approximate Entropy is the time-based function which measures the irregularity and randomness in EEG signal. The algorithm delivers a single value at the end of processing every data set. From the graphs showninfigure3 to figure 6 above, we can conclude that increase in value of ApEn indicates higher degree of randomness in EEG wave which in turn indicate presence of higher epileptic signal component in EEG signal. Thus, we can conclude that as the severity of epilepsy increases (from non-epileptic person to an epileptic person) the ApEn value also increases. The analysis of epilepsy can be further improved if machine learningalgorithms areappliedtotherecordedEEG signals under different medical test conditions. More data can be fed to the system to enhance the learningcapability of the system. More precise decision making is possible through enhancement in signal processing algorithms. Machine learning helps in better pattern recognition which in turn helps to achieve higher estimation accuracy. REFERENCES [1] Srinivasan, Vairavan, Chikkannan Eswaran, and Natarajan Sriraam, "Approximate entropy-based epileptic EEG detectionusing artificial neural networks," IEEE Transactions on information Technology in Biomedicine, vol. 11, no. 3, (2007): 288-295. [2] Pincus, Steven M. "Approximate entropyasa measureof system complexity," Proceedings of the National Academy of Sciences 88, no. 6 (1991): 2297-2301. [3] M. Teplan, “Fundamentals of EEG Measurement,” Institute of Measurement Science, Slovak Academy of Sciences, Dúbravská cesta 9841 04 Bratislava, Slovakia. [4] Helal, Alaa Eldeen Mahmoud, Ahmed Farag Seddik, Mohammed Ali Eldosoky, and Ayat Allah Farouk Hussein. "An Efficient Method for Epileptic Seizure Detection in Long-Term EEG Recordings," Journal of Biomedical Science and Engineering 7, no. 12 (2014): 963. [5] Kamath, Chandrakar. (2015).”Analysis of EEG signals in epileptic patients and control subjects using nonlinear deterministic chaotic and fractal quantifiers,” Science Postprint. 1. 10.14340/spp.2015.01A0003. [6] Andrzejak, Ralph G., Klaus Lehnertz, Florian Mormann, Christoph Rieke, Peter David, and Christian E. Elger. "Indications of nonlinear deterministic and finite- dimensional structures in time series of brain electrical activity: Dependence on recording region and brain state," Physical Review E 64, no. 6 (2001): 061907. [7] https://www.mathworks.com/matlabcentral/fileexchan ge/32427-fast-approximate-entropy