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IT in Industry, vol. 2, no. 2, 2014 Published online 16-Sep-2014
Copyright © Authors 62 ISSN: 2203-1731
Annotating Retina Fundus Images for Teaching
and Learning Diabetic Retinopathy Software
Rakibul Alam1
, Bruce Poon1, 2
, Mahmood Kazi Mohammed1, 3
, M. Ashraful Amin1
, Hong Yan2, 4
1
Computer Vision and Cybernetics Group, Department of Computer Science & Engineering, Independent University, Bangladesh
2
School of Electrical & Information Engineering, University of Sydney, NSW 2006, Australia
3
Sir Salimullah Medical College, 40/1, Tipu Sultan Rd, Dhaka, Bangladesh
4
Department of Electronic Engineering, City University of Hong Kong, Hong Kong, China
E-MAIL: rakeeb@live.com, bruce.poon@ieee.org, mkmohammed86@gmail.com, aminmdashraful@gmail.com, h.yan@cityu.edu.hk
Abstract— With the improvement in IT industry, more and
more application of computer software is introduced in teaching
and learning. In this paper, we discuss the development process
of such software. Diabetic Retinopathy is a common complication
for diabetic patients. It may cause sight loss if not treated early.
There are several stages of this disease. Fundus imagery is
required to identify the stage and severity of the disease. Due to
the lack of proper dataset of the fundus images and proper
annotation, it is very difficult to perform research on this topic.
Moreover, medical students are often facing difficulty with
identifying the diseases in later stage of their practice as they may
not have seen a sample of all of the stages of Diabetic Retinopathy
problems. To mitigate the problem, we have collected fundus
images from different geographic area of Bangladesh and
designed an annotation software to store information about the
patient, the infection level and their locations in the images.
Sometimes, it is difficult to select all appropriate pixels of the
infected region. To resolve the issue, we have introduced a K
nearest neighbor (KNN) based technique to accurately select the
region of interest (ROI). Once an expert (ophthalmologist) has
annotated the images, the software can be used by the students
for learning.
Keywords—teaching and learning Software; diabetic
retinopathy; medical image annotation; expert medical system; K-
nearest neighbor.
I. INTRODUCTION
Among many complications due to diabetics, diabetic
retinopathy [1] is the most common and can lead to severe eye
damages if not treated early. Sometimes, it starts with no early
warning. If untreated, it can cause severe proliferation. At the
early stage, namely nonproliferative stage, only micro-
aneurysms occur. Micro-aneurysms are round shaped swelling
in the retinal blood vessel. In the next phase, blood vessels that
is responsible to supply nourishment to retina starts to block.
This phase is moderate nonproliferative stage. If not treated,
more blood vessels are blocked and start depriving areas of
retina from blood supply which leads to proliferative stage. A
precise dataset is needed so that further study on those
retinopathy stages can be done. However, due to the lack of
such dataset, we have attempted to create one which contains
fundus images from different geographic areas of Bangladesh.
We have collected 625 fundus images from the health care
providers. Patients’ anonymity is ensured by producing a
unique image identification number for each patient. Besides,
we have developed software that can aid an expert to annotate
the infections and symptoms of different levels of retinopathy.
It is highly challenging for a human expert to accurately select
the region of infection in the image. Sometimes, an expert may
miss some pixels or regions here and there in the infected
region. To overcome the problem, we have designed a
neighborhood information based pixel clustering technique to
include or reject those which are not the part of infected
regions. This dataset with annotation software can be used later
in further investigations on the field of diabetic retinopathy. It
is also be a great aid to the medical students who are trying to
learn about the retinopathy levels. Machine learning based
models to correctly classify those levels are also possible using
such datasets. Previously, we have worked on automated
identification of retinal blood vessels [2] and optical disk [3]
that are applicable to retina based biometric applications [4].
However, for diabetic retinopathy teaching and learning facility
development, accuracy on annotation is on top priority while
faster annotation is on low priority.
Figure 1 shows the anatomy of a human eye where we can
see the location of Retina. Figure 2 shows retinal fundus image.
Figure 1. Anatomy of human eye
Fig. 1. Anatomy of a Human Eye
*This work is jointly supported by Independent University, Bangladesh
and University Grants Commission of Bangladesh under HEQEP Number:
CP-3359.
IT in Industry, vol. 2, no. 2, 2014 Published online 16-Sep-2014
Copyright © Authors 63 ISSN: 2203-1731
Fig. 2. Healthy retinal fundus image (left) and a retinal fundus image with
pathology (right)
II. DIABETIC RETINOPATHY
Diabetic Retinopathy is the most common diabetic eye
disease all over the world. The primary cause of the disease is
uncontrolled proliferation of retinal vessels. For some people
with diabetic retinopathy, blood vessels may swell and leak
fluid. For others, abnormal new blood vessels grow on the
surface of the retina. Retina is the light-sensitive tissue located
at the back of the eye. A healthy retina is necessary for good
vision. Different diabetic retinopathy levels are explained
below.
A. Nonproliferative Retinopathy
At this earliest stage, there is no symptom to any infections.
Nothing is visible to naked eye and patient also retains 20/20
vision. However, the tiny micro-aneurysms can be visible to
fundus imageries. The density of those micro-aneurysms
defines the level of non-proliferative retinopathy. Non
proliferative retinopathy can be subdivided into four categories
such as – very mild, mild. moderate and severe [1].
1) Very mild Nonproliferative Retinopathy.
In this stage only micro-aneurysms exists. Patient’s vision
is perfect. No other complication is visible.
2) Mild Nonproliferative Retinopathy.
Complication starts to grow in this stage. Micro-aneurysms,
retinal hemorrhage, cotton wool spots can be visible. No Intra-
retinal Micro-vascular Abnormality (IRMA) is visible.
3) Moderate Nonproliferative Retinopathy
In this stage, severe retinal hemorrhage exist in 1- 3
quadrants of the retina. IRMA exists and cotton wool spots are
commonly present in the retina.
4) Severe Nonproliferative Retinopathy
This is the most complicated nonproliferative stage. Severe
hemorrhage starts to grow in all four quadrants of the retina. A
significant amount of venous beading exists in 2 or more
quadrants. Sometimes, IRMA exists in more than one quadrant.
B. Proliferative Retinopathy
As the disease progresses, some blood vessels that nourish
the retina are blocked and stop supplying required nutrients to
some parts of retina. Those zones with malnutrition then send
signals to grow more blood vessels so that nutrients supply can
be possible.
More blood vessels are blocked, depriving several areas of
the retina with their blood supply. These areas of the retina
send signals to the body to grow new blood vessels for
nourishment. At this advanced stage, the signals sent by the
retina for nourishment trigger the growth of new blood vessels.
This condition is called proliferative retinopathy. These new
blood vessels are abnormal and fragile. They grow along the
retina and along the surface of the clear, vitreous gel that fills
the inside of the eye. By themselves, these blood vessels do not
cause symptoms or vision loss. However, they have thin,
fragile walls. If they leak blood, severe vision loss and even
blindness can result. Proliferative retinopathy can also be
categorized into two stages – mild moderate and high risk [1].
1) Mild Moderate Stage
New blood vessels on the disk start to appear. However, the
proliferation is not that severe.
2) High Risk Stage
In this stage, vessel proliferation becomes more severe and
it may blur the normal sight.
III. EXISTING DATASETS
We have collected almost all the publicly available retinal
fundus image datasets (databases). The Digital Retina Image
for Vessel Extraction (DRIVE) [5] database contains 40 color
retinal images, where 33 are healthy and 7 are pathological.
The VARPA Retina Images for Authentication (VARIA) [6]
database contains 233 grayscale images but with higher degree
of magnification. The numbers of healthy and pathological
images are not stated. Although VARIA dataset contains
multiple images of same individuals, the images are extremely
prone to noises due to the magnification or some other
unknown cause.
Fig. 3. Sample data from the DRIVE and MESSIDOR database
IT in Industry, vol. 2, no. 2, 2014 Published online 16-Sep-2014
Copyright © Authors 64 ISSN: 2203-1731
The VICAVR [7] dataset contains 58 color fundus images.
Two databases that are solely established for detection of
diabetic retinopathy are also used. They are standard diabetic
retinopathy database, DIARETDB_01 [8] and digital retina
images database, MESSIDOR [9]. DIARETDB_01 database
contains 89 color fundus images and MESSIDOR contains
1200 color retinal fundus images with low to mild pathologies.
Figure 3 shows sample images form DRIVE and MESSIDOR
datasets.
IV. DATA COLLECTION
We have discussed various existing datasets and their
characteristics in above section. However, due to the lack of
proper Diabetic Retinopathy dataset, we have attempted to
create a new dataset. Our main goal is to collect data from
different geographic areas with all kinds of variations so that it
reflects the whole picture of DR. To do so, we have contacted
different health care providers from Bangladesh and asked
them to provide the normal physiological information such as
age, sex, blood pressure, level of diabetics, pulse-rate, etc. We
have identified each patient with an image ID and made them
anonymous in order to protect their health related privacy.
Overall, we have collected 625 images from different
geographic areas. Figure. 4 shows the distribution of collected
fundus imagery from patients with positive diabetic
retinopathy.
V. PROPOSED MODEL
The image annotation facility is crucial to create retinal
dataset for diabetic retinopathy. An expert user can select the
diabetic retinopathy level by examining the whole picture.
There is a module where he can express his confidence level.
We also feel the necessity of a description field where expert
can express his remarks on the level of retinopathy. An array of
general information related to patients, such as age, sex, blood
pressure, level of diabetics, exposure to diabetics and pulse are
added for future investigations.
In this image annotation software, we have added eleven
different symptoms which are closely related to diabetic
retinopathy. Those are Micro-aneurysms, Retinal
Hemorrhages, Severe Retinal Hemorrhages, Exudates, Cotton
wool spots, IRMA, Moderate IRMA, Micro-vascular
Abnormalities, Venous Beading, New Vessels on Disk, and
New Vessels on elsewhere. A description field is added to
express the severity or mildness of the symptom.
The most crucial part of the software is the selection tools
that can aid the expert to select the appropriate location where
the symptom occurs. Our system provides four types of
selection tools such as polygon selection, eclipse selection,
point selection and free hand selection.
For data collection we have created an xml based archive
system that accumulates data from the software front end.
Because of the generic nature of xml tag based data archive, it
can be accessible to any system that can parse xml tags. A
fraction of a data archive file is shown Figure 5.
<root>
<imageName>IM0001.jpg</imageName>
<age>45</age>
<sex>m</sex>
<bloodPressure1>80</bloodPressure1>
<bloodPressure2>120</bloodPressure2>
<diabetics>7.0</diabetics>
<yearsDiabetics>3</yearsDiabetics>
<pulse>67</pulse>
<retinopathyLevel>2</retinopathyLevel>
<confidence>4</confidence>
<imageDescription>mild</imageDescription>
<objectCounter>2</objectCounter>
<object>
<objectName>Microaneurysms</objectName>
<description>mild</description>
<selectTool>eclipse</selectTool>
<positions>1709 380 139 107</positions>
<objectName>Cotton wool spots</objectName>
<description>mild</description>
<selectTool>polygon</selectTool>
<positions>1434 1430 1430 1502 1580 1702
</positions>
</object>
</root>
Fig. 5. Data Structure of the xml data sheet
We have created an adaptive user interface as shown in
Figure 6 that can aid to create datasets and help medical
students to learn about retinal disorders.
Mild Nonproliferative Retinopathy.
Moderate Nonproliferative Retinopathy
Severe Nonproliferative Retinopathy
Proliferative Retinopathy
Fig. 4. Geographic distribution of collected fundus images
IT in Industry, vol. 2, no. 2, 2014 Published online 16-Sep-2014
Copyright © Authors 65 ISSN: 2203-1731
It is clear from the Figure 5 that appropriate tags are used
for the data annotation in xml data archive. Due to the xml
based architecture, a hierarchical data structure is possible to
develop. The hierarchy is explained in Figure 7.
The data annotation hierarchy starts with root. Root
contains all the image information. Individual image contains
information about the patients, diabetic retinopathy level and
all the objects that are actually the symptoms of diabetic
retinopathy.
In the third level of hierarchy, the object contains the object
name (symptom name), description about the symptom, types
of selection tool used by expert and the positions of the
symptoms. Four selection tools that we have added in the data
annotation software are shown in Figure 8. Since we know that
it is difficult for human to exactly specify the Region of interest
(ROI), it is sometimes convenient to expand or shrink the ROI
based on the local neighborhood information. We have used
the K nearest neighbor [10] classifier to identify whether a
pixel is in the ROI or not.
Fig. 6. User interface of the DR data annotation software.
Root
Image Image Image…. … …
Image
Name
Age Sex ObjectsBlood
Pressure
pressure
Diabetics
Retinopathy
Level
Object
Name
Description Selection
Tools
Positions
Fig. 7. Hierarchical Data. ata
IT in Industry, vol. 2, no. 2, 2014 Published online 16-Sep-2014
Copyright © Authors 66 ISSN: 2203-1731
Fig. 8. Use of various Selection tools in our proposed model
Before the feature extraction, we have extracted the green
channel of the image. Tiny micro-aneurysms and other
symptoms are more visible in Green channel fundus image.
Green channel of the sample image is shown in Figure 9.
On the neighborhood, we have used a window based
classification. A predefined window is slide through the border
region. Average intensity and standard deviation are taken as
features to classify whether they are part of the original
selection or not. Figure 10 shows the corrected form of
selection after classifying the border regions with K-nearest
neighbor classifier.
Fig. 9. Green Channel of the fundus image
Fig. 10. ROI after KNN based border
VI. CONCLUSION AND FUTURE WORK
Diabetic retinopathy can lead to severe complications if it is
not treated in early stage. Investigations in this area are difficult
due to the lack of proper dataset. We have collected the fundus
images from different geographic locations of Bangladesh. A
software application with data achieve facility is introduced to
properly annotate the medical data. This dataset will also help
the medical students to learn the symptoms of the disease. To
ease the data annotation, we introduce KNN based classifier
that can select the region which add or shrink the region based
on local neighborhood information.
Although instrument for automatic detection of Diabetic
Retinopathy is available in the developed countries, they are
expensive to acquire. Our software system can provide an
economical alternative for the eye doctors and optometrists in
the developing countries to easily analysis Diabetic
Retinopathy with fundus images from their patients.
This research work can be further extended and improved.
A proper model can be developed to correctly classify all the
stages of DR. Improved hardware can provide faster annotation
in addition to accuracy.
ACKNOWLEDGMENT
The major work in this paper had been presented in the
International Conference on Information Technology and
Application (ICITA 2014), 1–4 July, 2014 in Sydney,
Australia. In addition, we addressed those issues arose during
ICITA 2014 for further improvement in our work.
We would like to think the anonymous volunteers who
have agreed to provide the retinal image and other personal
data for our research.
IT in Industry, vol. 2, no. 2, 2014 Published online 16-Sep-2014
Copyright © Authors 67 ISSN: 2203-1731
REFERENCES
[1] J. J. Kanski and B. Bowling, Clinical Opthalmologhy, 7th ed., Elsevier,
2011, pp. 535-554.
[2] M. Ashraful Amin and Hong Yan, “High Speed Detectionof Blood
Vessels in a Retinal Fundus Image using Phase Congruency,” Soft
Computing, 2011, Springer.
[3] M. Islamuddin Ahmed, M. Ashraful Amin, “High Speed Detection of
Optical Disc in Retinal Fundus Image”, Journal of Signal, Image and
Video Processing, 2012, Springer.
[4] M. Islamuddin Ahmed, M. Ashraful Amin, Bruce Poon, and Hong Yan
“Retina Based Biometric Authentication using Phase Congruency”,
IJMLC, 2013, Springer.
[5] Digital Retinal Image for Vessel Extraction (DRIVE). Available at :
http://www.isi.uu.nl/Research/Databases/DRIVE/
[6] VARPA Retina Images Authentication (VARIA) database. Available at :
http://www.varpa.es/varia.html
[7] VICAVR Database, http://www.varpa.es/vicavr.html
[8] DIARETDB_01: Standard Diabetic Retinopathy Database. Available at :
http://www2.it.lut.fi/project/imageret/diaretdb1/index.html
[9] MESSIDOR: Digital Retinal Images. Available at :
http://messidor.crihan.fr/download.php
[10] T. Cover, and P. Hart. "Nearest neighbor pattern classification."IEEE
Transl. Information Theory, vol. 13, issue. 1, pp. 21-27, 1967.

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Annotating Retina Fundus Images for Teaching and Learning Diabetic Retinopathy Software

  • 1. IT in Industry, vol. 2, no. 2, 2014 Published online 16-Sep-2014 Copyright © Authors 62 ISSN: 2203-1731 Annotating Retina Fundus Images for Teaching and Learning Diabetic Retinopathy Software Rakibul Alam1 , Bruce Poon1, 2 , Mahmood Kazi Mohammed1, 3 , M. Ashraful Amin1 , Hong Yan2, 4 1 Computer Vision and Cybernetics Group, Department of Computer Science & Engineering, Independent University, Bangladesh 2 School of Electrical & Information Engineering, University of Sydney, NSW 2006, Australia 3 Sir Salimullah Medical College, 40/1, Tipu Sultan Rd, Dhaka, Bangladesh 4 Department of Electronic Engineering, City University of Hong Kong, Hong Kong, China E-MAIL: rakeeb@live.com, bruce.poon@ieee.org, mkmohammed86@gmail.com, aminmdashraful@gmail.com, h.yan@cityu.edu.hk Abstract— With the improvement in IT industry, more and more application of computer software is introduced in teaching and learning. In this paper, we discuss the development process of such software. Diabetic Retinopathy is a common complication for diabetic patients. It may cause sight loss if not treated early. There are several stages of this disease. Fundus imagery is required to identify the stage and severity of the disease. Due to the lack of proper dataset of the fundus images and proper annotation, it is very difficult to perform research on this topic. Moreover, medical students are often facing difficulty with identifying the diseases in later stage of their practice as they may not have seen a sample of all of the stages of Diabetic Retinopathy problems. To mitigate the problem, we have collected fundus images from different geographic area of Bangladesh and designed an annotation software to store information about the patient, the infection level and their locations in the images. Sometimes, it is difficult to select all appropriate pixels of the infected region. To resolve the issue, we have introduced a K nearest neighbor (KNN) based technique to accurately select the region of interest (ROI). Once an expert (ophthalmologist) has annotated the images, the software can be used by the students for learning. Keywords—teaching and learning Software; diabetic retinopathy; medical image annotation; expert medical system; K- nearest neighbor. I. INTRODUCTION Among many complications due to diabetics, diabetic retinopathy [1] is the most common and can lead to severe eye damages if not treated early. Sometimes, it starts with no early warning. If untreated, it can cause severe proliferation. At the early stage, namely nonproliferative stage, only micro- aneurysms occur. Micro-aneurysms are round shaped swelling in the retinal blood vessel. In the next phase, blood vessels that is responsible to supply nourishment to retina starts to block. This phase is moderate nonproliferative stage. If not treated, more blood vessels are blocked and start depriving areas of retina from blood supply which leads to proliferative stage. A precise dataset is needed so that further study on those retinopathy stages can be done. However, due to the lack of such dataset, we have attempted to create one which contains fundus images from different geographic areas of Bangladesh. We have collected 625 fundus images from the health care providers. Patients’ anonymity is ensured by producing a unique image identification number for each patient. Besides, we have developed software that can aid an expert to annotate the infections and symptoms of different levels of retinopathy. It is highly challenging for a human expert to accurately select the region of infection in the image. Sometimes, an expert may miss some pixels or regions here and there in the infected region. To overcome the problem, we have designed a neighborhood information based pixel clustering technique to include or reject those which are not the part of infected regions. This dataset with annotation software can be used later in further investigations on the field of diabetic retinopathy. It is also be a great aid to the medical students who are trying to learn about the retinopathy levels. Machine learning based models to correctly classify those levels are also possible using such datasets. Previously, we have worked on automated identification of retinal blood vessels [2] and optical disk [3] that are applicable to retina based biometric applications [4]. However, for diabetic retinopathy teaching and learning facility development, accuracy on annotation is on top priority while faster annotation is on low priority. Figure 1 shows the anatomy of a human eye where we can see the location of Retina. Figure 2 shows retinal fundus image. Figure 1. Anatomy of human eye Fig. 1. Anatomy of a Human Eye *This work is jointly supported by Independent University, Bangladesh and University Grants Commission of Bangladesh under HEQEP Number: CP-3359.
  • 2. IT in Industry, vol. 2, no. 2, 2014 Published online 16-Sep-2014 Copyright © Authors 63 ISSN: 2203-1731 Fig. 2. Healthy retinal fundus image (left) and a retinal fundus image with pathology (right) II. DIABETIC RETINOPATHY Diabetic Retinopathy is the most common diabetic eye disease all over the world. The primary cause of the disease is uncontrolled proliferation of retinal vessels. For some people with diabetic retinopathy, blood vessels may swell and leak fluid. For others, abnormal new blood vessels grow on the surface of the retina. Retina is the light-sensitive tissue located at the back of the eye. A healthy retina is necessary for good vision. Different diabetic retinopathy levels are explained below. A. Nonproliferative Retinopathy At this earliest stage, there is no symptom to any infections. Nothing is visible to naked eye and patient also retains 20/20 vision. However, the tiny micro-aneurysms can be visible to fundus imageries. The density of those micro-aneurysms defines the level of non-proliferative retinopathy. Non proliferative retinopathy can be subdivided into four categories such as – very mild, mild. moderate and severe [1]. 1) Very mild Nonproliferative Retinopathy. In this stage only micro-aneurysms exists. Patient’s vision is perfect. No other complication is visible. 2) Mild Nonproliferative Retinopathy. Complication starts to grow in this stage. Micro-aneurysms, retinal hemorrhage, cotton wool spots can be visible. No Intra- retinal Micro-vascular Abnormality (IRMA) is visible. 3) Moderate Nonproliferative Retinopathy In this stage, severe retinal hemorrhage exist in 1- 3 quadrants of the retina. IRMA exists and cotton wool spots are commonly present in the retina. 4) Severe Nonproliferative Retinopathy This is the most complicated nonproliferative stage. Severe hemorrhage starts to grow in all four quadrants of the retina. A significant amount of venous beading exists in 2 or more quadrants. Sometimes, IRMA exists in more than one quadrant. B. Proliferative Retinopathy As the disease progresses, some blood vessels that nourish the retina are blocked and stop supplying required nutrients to some parts of retina. Those zones with malnutrition then send signals to grow more blood vessels so that nutrients supply can be possible. More blood vessels are blocked, depriving several areas of the retina with their blood supply. These areas of the retina send signals to the body to grow new blood vessels for nourishment. At this advanced stage, the signals sent by the retina for nourishment trigger the growth of new blood vessels. This condition is called proliferative retinopathy. These new blood vessels are abnormal and fragile. They grow along the retina and along the surface of the clear, vitreous gel that fills the inside of the eye. By themselves, these blood vessels do not cause symptoms or vision loss. However, they have thin, fragile walls. If they leak blood, severe vision loss and even blindness can result. Proliferative retinopathy can also be categorized into two stages – mild moderate and high risk [1]. 1) Mild Moderate Stage New blood vessels on the disk start to appear. However, the proliferation is not that severe. 2) High Risk Stage In this stage, vessel proliferation becomes more severe and it may blur the normal sight. III. EXISTING DATASETS We have collected almost all the publicly available retinal fundus image datasets (databases). The Digital Retina Image for Vessel Extraction (DRIVE) [5] database contains 40 color retinal images, where 33 are healthy and 7 are pathological. The VARPA Retina Images for Authentication (VARIA) [6] database contains 233 grayscale images but with higher degree of magnification. The numbers of healthy and pathological images are not stated. Although VARIA dataset contains multiple images of same individuals, the images are extremely prone to noises due to the magnification or some other unknown cause. Fig. 3. Sample data from the DRIVE and MESSIDOR database
  • 3. IT in Industry, vol. 2, no. 2, 2014 Published online 16-Sep-2014 Copyright © Authors 64 ISSN: 2203-1731 The VICAVR [7] dataset contains 58 color fundus images. Two databases that are solely established for detection of diabetic retinopathy are also used. They are standard diabetic retinopathy database, DIARETDB_01 [8] and digital retina images database, MESSIDOR [9]. DIARETDB_01 database contains 89 color fundus images and MESSIDOR contains 1200 color retinal fundus images with low to mild pathologies. Figure 3 shows sample images form DRIVE and MESSIDOR datasets. IV. DATA COLLECTION We have discussed various existing datasets and their characteristics in above section. However, due to the lack of proper Diabetic Retinopathy dataset, we have attempted to create a new dataset. Our main goal is to collect data from different geographic areas with all kinds of variations so that it reflects the whole picture of DR. To do so, we have contacted different health care providers from Bangladesh and asked them to provide the normal physiological information such as age, sex, blood pressure, level of diabetics, pulse-rate, etc. We have identified each patient with an image ID and made them anonymous in order to protect their health related privacy. Overall, we have collected 625 images from different geographic areas. Figure. 4 shows the distribution of collected fundus imagery from patients with positive diabetic retinopathy. V. PROPOSED MODEL The image annotation facility is crucial to create retinal dataset for diabetic retinopathy. An expert user can select the diabetic retinopathy level by examining the whole picture. There is a module where he can express his confidence level. We also feel the necessity of a description field where expert can express his remarks on the level of retinopathy. An array of general information related to patients, such as age, sex, blood pressure, level of diabetics, exposure to diabetics and pulse are added for future investigations. In this image annotation software, we have added eleven different symptoms which are closely related to diabetic retinopathy. Those are Micro-aneurysms, Retinal Hemorrhages, Severe Retinal Hemorrhages, Exudates, Cotton wool spots, IRMA, Moderate IRMA, Micro-vascular Abnormalities, Venous Beading, New Vessels on Disk, and New Vessels on elsewhere. A description field is added to express the severity or mildness of the symptom. The most crucial part of the software is the selection tools that can aid the expert to select the appropriate location where the symptom occurs. Our system provides four types of selection tools such as polygon selection, eclipse selection, point selection and free hand selection. For data collection we have created an xml based archive system that accumulates data from the software front end. Because of the generic nature of xml tag based data archive, it can be accessible to any system that can parse xml tags. A fraction of a data archive file is shown Figure 5. <root> <imageName>IM0001.jpg</imageName> <age>45</age> <sex>m</sex> <bloodPressure1>80</bloodPressure1> <bloodPressure2>120</bloodPressure2> <diabetics>7.0</diabetics> <yearsDiabetics>3</yearsDiabetics> <pulse>67</pulse> <retinopathyLevel>2</retinopathyLevel> <confidence>4</confidence> <imageDescription>mild</imageDescription> <objectCounter>2</objectCounter> <object> <objectName>Microaneurysms</objectName> <description>mild</description> <selectTool>eclipse</selectTool> <positions>1709 380 139 107</positions> <objectName>Cotton wool spots</objectName> <description>mild</description> <selectTool>polygon</selectTool> <positions>1434 1430 1430 1502 1580 1702 </positions> </object> </root> Fig. 5. Data Structure of the xml data sheet We have created an adaptive user interface as shown in Figure 6 that can aid to create datasets and help medical students to learn about retinal disorders. Mild Nonproliferative Retinopathy. Moderate Nonproliferative Retinopathy Severe Nonproliferative Retinopathy Proliferative Retinopathy Fig. 4. Geographic distribution of collected fundus images
  • 4. IT in Industry, vol. 2, no. 2, 2014 Published online 16-Sep-2014 Copyright © Authors 65 ISSN: 2203-1731 It is clear from the Figure 5 that appropriate tags are used for the data annotation in xml data archive. Due to the xml based architecture, a hierarchical data structure is possible to develop. The hierarchy is explained in Figure 7. The data annotation hierarchy starts with root. Root contains all the image information. Individual image contains information about the patients, diabetic retinopathy level and all the objects that are actually the symptoms of diabetic retinopathy. In the third level of hierarchy, the object contains the object name (symptom name), description about the symptom, types of selection tool used by expert and the positions of the symptoms. Four selection tools that we have added in the data annotation software are shown in Figure 8. Since we know that it is difficult for human to exactly specify the Region of interest (ROI), it is sometimes convenient to expand or shrink the ROI based on the local neighborhood information. We have used the K nearest neighbor [10] classifier to identify whether a pixel is in the ROI or not. Fig. 6. User interface of the DR data annotation software. Root Image Image Image…. … … Image Name Age Sex ObjectsBlood Pressure pressure Diabetics Retinopathy Level Object Name Description Selection Tools Positions Fig. 7. Hierarchical Data. ata
  • 5. IT in Industry, vol. 2, no. 2, 2014 Published online 16-Sep-2014 Copyright © Authors 66 ISSN: 2203-1731 Fig. 8. Use of various Selection tools in our proposed model Before the feature extraction, we have extracted the green channel of the image. Tiny micro-aneurysms and other symptoms are more visible in Green channel fundus image. Green channel of the sample image is shown in Figure 9. On the neighborhood, we have used a window based classification. A predefined window is slide through the border region. Average intensity and standard deviation are taken as features to classify whether they are part of the original selection or not. Figure 10 shows the corrected form of selection after classifying the border regions with K-nearest neighbor classifier. Fig. 9. Green Channel of the fundus image Fig. 10. ROI after KNN based border VI. CONCLUSION AND FUTURE WORK Diabetic retinopathy can lead to severe complications if it is not treated in early stage. Investigations in this area are difficult due to the lack of proper dataset. We have collected the fundus images from different geographic locations of Bangladesh. A software application with data achieve facility is introduced to properly annotate the medical data. This dataset will also help the medical students to learn the symptoms of the disease. To ease the data annotation, we introduce KNN based classifier that can select the region which add or shrink the region based on local neighborhood information. Although instrument for automatic detection of Diabetic Retinopathy is available in the developed countries, they are expensive to acquire. Our software system can provide an economical alternative for the eye doctors and optometrists in the developing countries to easily analysis Diabetic Retinopathy with fundus images from their patients. This research work can be further extended and improved. A proper model can be developed to correctly classify all the stages of DR. Improved hardware can provide faster annotation in addition to accuracy. ACKNOWLEDGMENT The major work in this paper had been presented in the International Conference on Information Technology and Application (ICITA 2014), 1–4 July, 2014 in Sydney, Australia. In addition, we addressed those issues arose during ICITA 2014 for further improvement in our work. We would like to think the anonymous volunteers who have agreed to provide the retinal image and other personal data for our research.
  • 6. IT in Industry, vol. 2, no. 2, 2014 Published online 16-Sep-2014 Copyright © Authors 67 ISSN: 2203-1731 REFERENCES [1] J. J. Kanski and B. Bowling, Clinical Opthalmologhy, 7th ed., Elsevier, 2011, pp. 535-554. [2] M. Ashraful Amin and Hong Yan, “High Speed Detectionof Blood Vessels in a Retinal Fundus Image using Phase Congruency,” Soft Computing, 2011, Springer. [3] M. Islamuddin Ahmed, M. Ashraful Amin, “High Speed Detection of Optical Disc in Retinal Fundus Image”, Journal of Signal, Image and Video Processing, 2012, Springer. [4] M. Islamuddin Ahmed, M. Ashraful Amin, Bruce Poon, and Hong Yan “Retina Based Biometric Authentication using Phase Congruency”, IJMLC, 2013, Springer. [5] Digital Retinal Image for Vessel Extraction (DRIVE). Available at : http://www.isi.uu.nl/Research/Databases/DRIVE/ [6] VARPA Retina Images Authentication (VARIA) database. Available at : http://www.varpa.es/varia.html [7] VICAVR Database, http://www.varpa.es/vicavr.html [8] DIARETDB_01: Standard Diabetic Retinopathy Database. Available at : http://www2.it.lut.fi/project/imageret/diaretdb1/index.html [9] MESSIDOR: Digital Retinal Images. Available at : http://messidor.crihan.fr/download.php [10] T. Cover, and P. Hart. "Nearest neighbor pattern classification."IEEE Transl. Information Theory, vol. 13, issue. 1, pp. 21-27, 1967.