Abstract
We present a novel and fully automated fundus image processing technique for glaucoma prescreening based on the rim-to-disc ratio (RDR). The technique accurately segments the optic disc and optic cup and then computes the RDR based on which it is possible to differentiate a normal fundus from a glaucomatous one. The technique performs a further categorization into normal, moderate, or severely glaucomatous classes following the disc-damage-likelihood scale (DDLS). To the best of our knowledge, this is the first engineering attempt at using RDR and DDLS to perform glaucoma severity assessment. The segmentation of the optic disc and cup is based on the active disc, whose parameters are optimized to maximize the local contrast. The optimization is performed efficiently by means of a multiscale representation, accelerated gradient-descent, and Green’s theorem. Validations are performed on several publicly available databases as well as data provided by manufacturers of some commercially available fundus imaging devices. The segmentation and classification performance is assessed against expert clinician annotations in terms of sensitivity, specificity, accuracy, Jaccard, and Dice similarity indices. The results show that RDR based automated glaucoma assessment is about 8% to 10% more accurate than a cup-to-disc ratio (CDR) based system. An ablation study carried out considering the ground-truth expert outlines alone for classification showed that RDR is superior to CDR by 5.28% in a two-stage classification and about 3.21% in a three-stage severity grading.
Subject terms: Diagnosis, Biomedical engineering, Electrical and electronic engineering
Introduction
The optic disc is a small blind spot on the surface of the retina and does not contain any photoreceptors. Millions of nerve fibers run from the retina to the optic nerve and converge at the optic disc. The optic disc has three distinct regions: a central white depression called the cup, a peripheral ring-shaped region called the neuroretinal rim, and the optic nerves. Glaucoma is caused by high intraocular fluid pressure created by the abnormal production or drainage of the aqueous humor circulating between the cornea and the lens inside the eye. Glaucoma is an optic neuropathy1 – it is a chronic, irreversible, and progressive eye disease that involves loss of retinal nerve fiber layer in a characteristic pattern2. It is a leading cause of visual disability and a global public health issue. According to the World Health Organization (WHO), glaucoma is the second leading cause of blindness, after cataract. It is estimated that, by 2020, the total number of glaucoma cases worldwide would be well over 80 million3. Early detection and diagnosis of glaucoma requires a careful and comprehensive eye examination, and modern digital technology could aid in rapid assessment.
Since glaucoma alters the optic disc topography, commonly known as cupping, and associated loss of the visual field, it is treated based upon the structural appearance of the optic disc and its function by means of a fundus image. The various forms of imaging such as Heidelberg retinal tomography (HRT), scanning laser polarimetry (SLP), and optical-coherence tomography (OCT), permit quantitative measurement of the optic disc and retinal nerve fiber layer (RNFL) structure4. Optical-coherence tomography detects damage of the RNFL, whereas HRT characterizes changes in the optic nerve topography. Giaconi et al. observed that these imaging modalities complement each other very well, but their sensitivity and specificity are not adequate from diagnostic perspective4. Of late, several portable and cost-effective fundus imaging devices and fundus-on-phone (FOP) devices have become available. It is with such devices in mind that we address the goal of developing robust image processing techniques for glaucoma assessment with severity grading and create easy-to-use software that would be suitable for deployment in mass screening programs.
To identify the onset of glaucoma and follow-up on its progression, it is important to quantify the size and shape of the optic disc, cup, and neuroretinal rim4,5. The cup-to-disc ratio (CDR) proposed by Armaly et al.6, rim-to-disc ratio (RDR) based on disc-damage-likelihood-scale (DDLS) proposed by Spaeth et al.7, and a check for the pattern of neuroretinal rim-widths: Inferior ≥ Superior ≥ Nasal ≥ Temporal (ISNT), proposed by Jonas et al.8 are important parameters that the ophthalmologists rely on. However, CDR has been the most popular measure that the biomedical engineering community has relied on. The goal of this paper is to assess the importance of the other measures such as RDR and ISNT rim-widths9–13 in comparison with CDR and determine which one offers a more reliable and accurate assessment. Automatic determination of these parameters is important as manual annotation of the optic disc and cup and subsequent computation of the parameters is a tedious and time-consuming process. Moreover, fatigue may result in variability and loss of consistency in the manual outlining process. Therefore, automated outlining of the optic disc and cup and determination of CDR/RDR/ISNT rim-widths (cf. Fig. 1) become crucial6,7,14.
During the past decade, efficient methods have been developed to segment the optic disc, but optic cup segmentation has not received as much importance. A review of the literature on segmentation is presented in Section S1 of Supporting Information. Since 1960s, CDR has been the most commonly used parameter for measuring the relative amount of cupping. However, it has two limitations: (i) it does not reflect the size of the optic disc and the position of the cup; and (ii) it does not take into account the amount of loss of nerve fibers in the neuroretinal rim, which directly determines the loss of the visual field. An optic cup that is eccentric is far more likely to be glaucomatous than a concentric one15–18. Figure 2 serves as an illustration to show that the CDR is not reliable in such scenarios. From a clinical perspective, ISNT has been shown to be inaccurate for performing glaucoma assessment12,13. The RDR parameter with DDLS takes into account the size of the optic disc, position of the optic cup, the narrowest neuroretinal rim-width, and thereby accurately captures the disc abnormality. Rim-to-disc ratio also has the advantage that it overcomes the effect of the optic disc size, which is highly variable in a population19. The DDLS has been validated against visual field loss and found to be more reproducible and reliable than HRT7,15–18. Abdul Majid et al. conducted a clinical study on 149 patients and categorized them as normal, glaucoma suspect, or with glaucoma, employing a DDLS based grading. They established that the DDLS has the best predictive power and showed that it exhibits a close correlation with visual field, CDR, and OCT parameters20. A related study by Pahlitzsch et al. on patients with preperimetric primary open-angle glaucoma reinforced the predictive power of the DDLS, which makes it an important tool in diagnosing glaucoma21. Kara-José et al. carried out optic disc clinical evaluation with the DDLS system and the CDR, which showed high accuracy in distinguishing healthy eyes from glaucomatous ones. They showed that the DDLS has moderate-to-strong correlations with most anatomical and functional tests employed for detecting glaucoma22. Danesh-Meyer et al. conducted a HRT-based clinical study on 110 patients for glaucoma prescreening and evaluated the relationship between the DDLS score, global and sectoral optic disc parameters and visual field indices23. A recent study by Hornová et al. established that evaluation of the optic nerve head with the DDLS has a high correlation with visual field and the data obtained from HRT-II24. Spaeth and Reddy compared various forms of optic nerve imaging such as ophthalmoscopy, fundus photography, OCT, HRT, scanning laser polarimetry, and argued that ophthalmoscopy and fundus photography remain the gold standard of imaging25. To the best of our knowledge, a fundus-image-based computer-aided technique using RDR and DDLS-based severity grading has not been reported in the literature although there is strong clinical evidence in its favour. The objective of this paper is to precisely fill this engineering gap.
Methods
The first step in our approach is the segmentation of the optic disc and cup, which is carried out using the concept of active discs that we introduced recently26,27. The segmentation is based on the active disc, which comprises two concentric circular discs centered at the origin and parameterized as follows:
1 |
for i = 1, 2, and , where ri for i = 1, 2 represents the radius of the outer and inner discs, which are set to 1 and , respectively. An example of such a template is shown in Fig. 3(a). The concentric discs with isotropic scaling and translation are given by
2 |
where i = 1, 2, and (X1, Y1), and (X2, Y2) are the outer and inner boundaries, respectively, R represents the scale parameter and (xc, yc) are the translational parameters, amounting to a total of three degrees of freedom. For brevity of notation, we replace (xi(t), yi(t)) and (Xi(t), Yi(t)) with (xi, yi) and (Xi, Yi), respectively. The active disc energy is based on a normalized contrast, which considers the area inside the inner disc as the foreground and the annular region as the background. For an image f, let R1and R2 be the regions enclosed by the outer and inner discs, respectively. The objective function is chosen to be
3 |
where E1 and E2 are the image energies in the regions R1and R2, respectively. Optimizing E would maximize the contrast between the two regions. The active disc is evolved from an initialization towards the boundary of the optic disc such that the energy is minimized. Figure 3(b) gives an example of the optimal fit contour.
Initialization
Accurate initialization is essential for reliable segmentation. We develop an automatic initialization technique using a multiscale normalized matched filter, inspired by the pyramidal decomposition method of Lalonde et al.28. To begin with, we construct a three-level pyramid. At the lowest level, the cross-correlation between the fundus image and a natural optic disc template is computed. The peak in the result is selected for initializing the template at that scale. The peak location (xp, yp) in level 3 is mapped to the image at the top of the pyramid. After localization, the region of interest surrounding the optic disc is chosen for subsequent analysis. The details of the initialization procedure are given in Section S2 of Supporting Information.
Optic disc segmentation
We use the red channel of the monocular color fundus image for disc segmentation, the reason being that the blood vessels and optic nerve occlusions get de-emphasized compared with the other channels or the grayscale version. Also, the optic disc appears brightest in the red channel, which goes well with our local-contrast-based segmentation strategy. The segmentation is accelerated using a multiscale strategy. The best-fit disc outline is obtained on the coarse-level representation at the bottom of the image pyramid. The converged result is used to determine the initialization for the immediate next finer resolution image. This process is repeated all the way to the top of the pyramid resulting in the final outline. The details of the active disc formulation, optimization and means to enhance computational efficiency are given in Section S3 of Supporting Information.
Optic cup segmentation
For cup segmentation, we extract the green channel as it has a higher contrast. We use Otsu’s multilevel thresholding algorithm29,30 to classify and cluster the pixels corresponding to the optic cup, and then refine it using the active disc. Examples of coarse optic cup segmentation achieved using Otsu’s algorithm are provided in Section S4 of Supporting Information. We found that a four-level thresholding scheme works well for clustering the optic cup pixels. The procedure used to obtain the optic cup boundary is similar to that explained in Section S3 of the Supporting Information.
Performance metrics
Sensitivity, specificity, accuracy, Jaccard, and Dice similarity indices are the standard comparison metrics31,32 used in medical image segmentation. They are based on true positives (TP), true negatives (TN), false positives (FP), and false negatives (FN). Sensitivity is the proportion of positives that are correctly identified as positives, whereas specificity is the proportion of negatives that are correctly identified as negatives. Accuracy is the degree of closeness between the algorithm segmentation and the expert clinician segmentation.
The Jaccard and Dice similarity indices are defined as Jaccard and Dice , respectively, where A and M represent the optic disc or cup region segmented by the algorithm and the manual segmentation provided by the clinician, respectively.
Parameters of clinical relevance
The clinically relevant parameters that we shall consider are: CDR6, RDR followed by DDLS7, and a check for the ISNT pattern of neuroretinal rim-widths8. It turns out that the geometry of the disc and cup outlines obtained after segmentation provides a precise mathematical basis for determining the smallest neuroretinal rim-width. We estimate the vertical height of the optic disc and cup and also narrowest rim-width for the computation of CDR, RDR, and inferior, superior, nasal, and temporal rim-widths for checking the ISNT pattern. We follow the International Classification of Diseases (ICD-9) rule33 based on CDR for a three-stage assessment of glaucoma severity as follows: normal (0 ≤ CDR ≤ 0.5); moderate (0.5 ≤ CDR ≤ 0.8); and severely glaucomatous (0.8 ≤ CDR ≤ 1).
Severity assessment of glaucoma using DDLS based on RDR
The DDLS takes into account the optic disc size and the optic cup location and is a reliable indicator of the visual field loss. The smallest neuroretinal rim-width is an important parameter for DDLS-based glaucoma stage analysis. The reliability of DDLS has been proved by Henderer et al.16,17 and its clinical relevance compared with CDR and HRT for glaucoma diagnosis has been established by Meyer et al.18. The smallest neuroretinal rim-width can be obtained by considering the geometry of two non-concentric circles one fully inside the other as depicted in Fig. 4. Circles with centers O1 and O2 represent the optic cup and disc, respectively. It can be established geometrically that the line joining the centers when extended to the periphery of the outer disc determines the smallest neuroretinal rim-width. Specifically, with respect to Fig. 4, the line segment PQ gives the desired rim-width. Based on the narrowest rim-width, glaucomatous conditions can be categorized into 8 or 10 stages as given in Table 1. We consider the following three-stage classification in accordance with the modified rule proposed by Spaeth et al.15 and Henderer et al.16, which has now become an internationally accepted guideline:
Not definitely damaged (normal);
Asymptomatic glaucoma damage (moderate); and
Glaucomatous disease/disability (severe).
Table 1.
DDLS stage (Spaeth et al.7) | DDLS stage (Spaeth et al.15 and Henderer et al.16) | Rim-to-disc ratio (RDR) range | Glaucomatous condition |
---|---|---|---|
0 (0a and 0b) | 1 and 2 | 0.30 ≤ RDR ≤ 0.50 | Not definitely damaged (Normal) |
1 | 3 | 0.20 < RDR ≤ 0.29 | |
2 | 4 | 0.10 < RDR ≤ 0.19 | |
3 | 5 | 0.01 < RDR 0.10 | Asymptomatic glaucoma damage (Moderate) |
4 | 6 | No rim < 45° | |
5 | 7 | No rim 45°–90° | |
6 | 8 | No rim 90°–180° | Glaucomatous disease/disability (Severe) |
7 (7a and 7b) | 9 and 10 | No rim < 180° |
For comparison, the classification proposed by Spaeth et al.7 is also shown.
Database validation
In this section, we examine the performance of the proposed technique on several retinal fundus image databases varying in size, resolution, contrast, and illumination. The publicly available databases used are Messidor34, Drishti-GS35, DiaretDB136, Drive37, and Drions-DB38, containing 1200, 101, 89, 40, and 110 retinal fundus images, respectively. The locally obtained databases are from Forus Health Pvt. Ltd.39 and Bosch Eye Care Solutions40 containing 126 and 60 retinal fundus images, respectively. This amounts to a total of 1726 images. The Forus desktop fundus-imaging camera results in a four-megapixel image, whereas the Bosch handheld device produces images at five-megapixel resolution. The Messidor, Drishti-GS, and Drions-DB databases provide the ground-truth outlines for the optic disc. The Drishti-GS database additionally provides the ground-truth outlines for the optic cup. Manual outlines of the optic disc and cup were provided by two ophthalmologists for the images taken from the Forus and Bosch databases as well as for 386 images drawn randomly from the other databases. This amounts to a total of 1597 images for assessing the optic disc segmentation performance and 436 images for assessing the cup segmentation performance. According to the expert assessment, out of the 436 images, 358 are normal and 78 are glaucomatous considering a two-stage classification. Considering a three-stage severity grading gave rise to 309 normal, 118 moderately glaucomatous, and 9 severely glaucomatous cases.
Software
The proposed approach has been implemented in Java as an ImageJ plugin41,42. A batch-processing ImageJ macro was developed to automatically handle all the images in a database. The performance evaluation was carried out on Mac OS X 2.7 GHz, Intel Core i5 machine. We have also developed iOS and Android apps that can be easily integrated into modern-day smartphone-based glaucoma-prescreening devices. Screenshots of the iOS app are shown in Section S5 of Supporting Information.
Results
The performance of the proposed multiscale normalized matched filtering technique is given in Table 2. We observe that the localization accuracy is at 100% for four out of seven databases, and greater than 97% for the remaining. The low processing time of 0.32 seconds per image is a direct advantage of employing the multiscale strategy. The optic disc and cup outlines are shown in Fig. 5 for some representative images taken from the databases. Figure 6 shows the algorithm outlines in comparison with the expert outlines. The segmentation performance of the proposed method and the average time taken are summarized in Tables 3 and 4. A comparison of the performance of the proposed method with the state-of-the-art techniques is shown in Section S6 of Supporting Information. The performance metrics indicate that the proposed technique gives outlines that have a high degree of agreement with the expert markings over several databases. Tables 5 and 6 show the performance of the RDR in comparison with CDR based on ICD-9 rule and ISNT for two-stage and three-stage glaucoma classification, respectively. The overall classification accuracy (OCA) over a database is defined as the ratio of the number of images correctly classified to the total number of images used for evaluation from that database. The OCA is higher for RDR based assessment compared with CDR and ISNT. Specifically, the accuracy of RDR is superior to CDR by 7.8% for a two-stage classification and 9.64% for a three-stage severity grading.
Table 2.
Algorithm | Database and # of images used | Localization accuracy in % | Average detection time per image in seconds |
---|---|---|---|
Proposed method | Drishti-GS (101) | 99.01 | 0.32 |
Drions-DB (110) | 100.00 | ||
Drive (40) | 100.00 | ||
DiaretDB1 (89) | 97.75 | ||
Messidor (1200) | 99.33 | ||
Forus (126) | 100.00 | ||
Bosch (60) | 100.00 |
Table 3.
Database and number of images used | Sensitivity | Specificity | Accuracy | Jaccard index | Dice index | Average time taken per image in seconds |
---|---|---|---|---|---|---|
Drishti-GS (101) | 0.9962 | 0.9698 | 0.9732 | 0.8707 | 0.9282 | 7.35 |
Drions-DB (110) | 0.8410 | 0.9960 | 0.9850 | 0.8341 | 0.9062 | 4.45 |
Messidor (1200) | 0.8840 | 0.9894 | 0.9882 | 0.7858 | 0.8760 | 6.34 |
Forus (126) | 0.9457 | 0.9957 | 0.9911 | 0.9319 | 0.9642 | 6.22 |
Bosch (60) | 0.9649 | 0.9994 | 0.9968 | 0.9109 | 0.9531 | 6.35 |
Table 4.
Database and number of images used | Sensitivity | Specificity | Accuracy | Jaccard index | Dice index | Average time taken per image in seconds |
---|---|---|---|---|---|---|
Drishti-GS (50) | 0.8589 | 0.9698 | 0.9690 | 0.6143 | 0.7532 | 5.46 |
Drions-DB (100) | 0.6175 | 0.9979 | 0.9884 | 0.5898 | 0.7300 | 3.54 |
Messidor (100) | 0.8357 | 0.9883 | 0.9823 | 0.5911 | 0.7303 | 4.35 |
Forus (126) | 0.7466 | 0.9952 | 0.9867 | 0.6801 | 0.8027 | 4.12 |
Bosch (60) | 0.7584 | 0.9959 | 0.9917 | 0.5804 | 0.7213 | 4.28 |
Table 5.
Database and number of images used | Ground truth | RDR-based results | CDR-based results | ISNT-based results | |||||||
---|---|---|---|---|---|---|---|---|---|---|---|
N | G | N | G | OCA | N | G | OCA | N | G | OCA | |
Drishti-GS (50) | 16 | 34 | 12 | 38 | 43/50 | 21 | 29 | 40/50 | 08 | 42 | 37/50 |
Drions-DB (100) | 90 | 10 | 88 | 12 | 85/100 | 79 | 21 | 80/100 | 70 | 30 | 71/100 |
Messidor (100) | 92 | 08 | 91 | 09 | 91/100 | 82 | 18 | 80/100 | 75 | 25 | 73/100 |
Forus (126) | 100 | 26 | 99 | 27 | 124/126 | 105 | 21 | 110/126 | 86 | 40 | 100/126 |
Bosch (60) | 60 | 00 | 59 | 01 | 59/60 | 58 | 02 | 58/60 | 53 | 07 | 50/60 |
Consolidated (436 images) | 358 | 78 | 349 | 87 | 402/436 (92.20%) | 345 | 91 | 368/436 (84.40%) | 292 | 144 | 331/436 (75.92%) |
(N – Normal; G – Glaucomatous; OCA – Overall Classification Accuracy).
Table 6.
Database and number of images used | Ground truth | RDR-based results (DDLS) | CDR-based results (ICD-9) | ||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
N | Mod | S | N | Mod | S | OCA | N | Mod | S | OCA | |
Drishti-GS (50) | 13 | 32 | 05 | 19 | 31 | 00 | 42/50 | 07 | 42 | 01 | 36/50 |
Drions-DB (100) | 78 | 22 | 00 | 77 | 20 | 03 | 82/100 | 73 | 25 | 02 | 78/100 |
Messidor (100) | 58 | 41 | 01 | 60 | 40 | 00 | 84/100 | 52 | 47 | 01 | 70/100 |
Forus (126) | 100 | 23 | 03 | 97 | 27 | 02 | 121/126 | 88 | 37 | 01 | 106/126 |
Bosch (60) | 60 | 00 | 00 | 59 | 01 | 00 | 59/60 | 56 | 04 | 00 | 56/60 |
Consolidated (436 images) | 309 | 118 | 09 | 312 | 119 | 05 | 388/436 (89%) | 312 | 119 | 05 | 346/436(79.36%) |
(N – Normal; Mod – Moderate; S – Severe; OCA – Overall Classification Accuracy).
In order to remove the influence of the segmentation method on the claim, we conducted an ablation study where we also considered the classification performance purely based on the expert outlines (Tables 7 and 8). From these results, we observe that the RDR-based two-stage classification is 5.28% superior to the CDR-based one. In the case of a three-stage severity grading, the accuracy improvement offered by RDR over CDR is 3.21%.
Table 7.
Database and number of images used | RDR-based assessment | CDR-based assessment | ||||
---|---|---|---|---|---|---|
Sensitivity | Specificity | Accuracy | Sensitivity | Specificity | Accuracy | |
Drishti-GS (50) | 0.9706 | 0.9375 | 0.9600 | 0.9412 | 0.7500 | 0.8800 |
Drions-DB (100) | 1.0000 | 0.9560 | 0.9600 | 1.0000 | 0.9121 | 0.9200 |
Messidor (100) | 1.0000 | 0.9560 | 0.9600 | 0.8889 | 0.8791 | 0.8800 |
Forus (126) | 0.9630 | 0.9697 | 0.9683 | 0.8889 | 0.9091 | 0.9048 |
Bosch (60) | — | 1.0000 | 1.0000 | — | 1.0000 | 1.0000 |
Consolidated (436 images) | 0.9625 | 0.9663 | 0.9656 | 0.9241 | 0.9104 | 0.9128 |
Table 8.
Database and number of images used | RDR-based assessment | CDR-based assessment | ||||
---|---|---|---|---|---|---|
Sensitivity | Specificity | Accuracy | Sensitivity | Specificity | Accuracy | |
Drishti-GS (50) | 0.8421 | 0.8333 | 0.8400 | 0.8158 | 0.7500 | 0.8000 |
Drions-DB (100) | 0.8871 | 0.8861 | 0.8800 | 0.6667 | 0.8861 | 0.8400 |
Messidor (100) | 0.8667 | 0.9091 | 0.8900 | 0.8444 | 0.8909 | 0.8700 |
Forus (126) | 0.8462 | 0.9100 | 0.8968 | 0.8077 | 0.8609 | 0.8492 |
Bosch (60) | — | 1.0000 | 1.0000 | — | 1.0000 | 1.0000 |
Consolidated (436 images) | 0.8538 | 0.9183 | 0.8991 | 0.8000 | 0.8954 | 0.8679 |
The preceding study establishes the superiority of RDR-based glaucoma classification over a CDR-based one.
Conclusions
In this paper, we developed a new method to perform severity grading of glaucoma based on RDR. We showed that the classification accuracy is higher when one uses the RDR-based DDLS instead of the frequently employed CDR, both in case of automated segmentation as well as expert annotation. From a clinical perspective also, RDR is more representative of the severity of the glaucoma than CDR as it captures the loss of neuroretinal fiber more accurately. The high accuracy is reflected in both two-stage and three-stage glaucoma classification. As far as estimating the RDR is concerned, we deployed a novel active disc template based method operating in a multiscale framework. The optic disc and cup segmentation results were found to be in high agreement with the expert outlines over a large number of images taken from various databases. In keeping with the contemporary and game-changing trend of developing smartphone-based eye-care solutions, we have also developed associated software in Java and Apps for Android and iOS devices, which operate in real-time on the device without the need for processing on a centralized server or in the cloud. These software solutions are particularly attractive for triaging applications using modern day handheld fundus imaging devices, which are heavily deployed for mass-screening purposes in the third-world countries in particular those in south Asia and Africa.
Supplementary information
Acknowledgements
The authors would like to thank the providers of publicly available fundus image database used in this study, and Forus Health Pvt. Ltd. and Bosch Eye Care Solutions, Bengaluru, India, for providing fundus images acquired using their devices. Thanks also go out to Dr. Ravi Prasad K. J. for technical discussions on the significance of RDR and Kaushik Sambamurthy, Rittwik Adhikari, Subramanya Jois, and Harsha Sridhar for developing the iOS and Android Apps. This research is funded under the IMPRINT India Initiative (Domain: Healthcare; Project code: 6013) by the Ministry of Human Resource Development (MHRD), Government of India. The authors would also like to thank the anonymous reviewers for their constructive comments, which greatly enhanced the quality of this contribution.
Author Contributions
C.S.S. conceived the project and directed the research; J.R.H.K. designed and implemented the project; J.R.H.K. developed the optimization modules, Java-based ImageJ plugins, and carried out experimental validations and analyzed the results; Y.K. and R.J. analyzed the fundus images clinically; J.R.H.K. and C.S.S. wrote the paper.
Competing Interests
The authors declare no competing interests.
Footnotes
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Contributor Information
J. R. Harish Kumar, Email: harishj@iisc.ac.in.
Chandra Sekhar Seelamantula, Email: chandrasekhar@iisc.ac.in.
Supplementary information
Supplementary information accompanies this paper at 10.1038/s41598-019-43385-2.
References
- 1.Casson RJ, et al. Definition of glaucoma: clinical and experimental concepts. Clin. Experiment. Ophthalmol. 2012;40:341–349. doi: 10.1111/j.1442-9071.2012.02773.x. [DOI] [PubMed] [Google Scholar]
- 2.Abramoff MD, Garvin MK, Sonka M. Retinal imaging and image analysis. IEEE Reviews in Biomedical Engineering. 2010;3:169–208. doi: 10.1109/RBME.2010.2084567. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Quigley HA, Broman AT. The number of people with glaucoma worldwide in 2010 and 2020. Br. J. Ophthalmol. 2006;90:262–267. doi: 10.1136/bjo.2005.081224. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Giaconi, J. A., Law, S. K., Coleman, A. L. & Caprioli, J. Pearls of Glaucoma Management. Springer, USA (2010).
- 5.Hoffmann EM, Zangwill LM, Crowston JG, Weinreb RN. Optic disk size and glaucoma. Surv. Ophthalmol. 2007;52:32–49. doi: 10.1016/j.survophthal.2006.10.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Armaly MF, Sayegh RE. The cup/disc ratio: The findings of tonometry and tonography in the normal eye. Archives of Ophthalmology. 1969;82:191–196. doi: 10.1001/archopht.1969.00990020193008. [DOI] [PubMed] [Google Scholar]
- 7.Spaeth GL, et al. The disc damage likelihood scale: Reproducibility of a new method of estimating the amount of nerve damage caused by glaucoma. Trans. Am. Ophthalmol. Soc. 2002;100:181–186. [PMC free article] [PubMed] [Google Scholar]
- 8.Jonas JB, Gusek GC, Naumann GO. Optic disc, cup and neuro-retinal rim size, configuration, and correlations in normal eyes. Invest. Ophthalmol. Vis. Sci. 1988;29:1151–1158. [PubMed] [Google Scholar]
- 9.Strouthidis NG, et al. Factors affecting the test-retest variability of Heidelberg retina tomograph and Heidelberg retina tomograph II measurements. Br. J. Ophthalmol. 2005;89:1427–1432. doi: 10.1136/bjo.2005.067298. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Greaney MJ, et al. Comparison of optic nerve imaging methods to distinguish normal eyes from those with glaucoma. Invest. Ophthalmol. Vis. Sci. 2002;43:140–145. [PubMed] [Google Scholar]
- 11.Lichter PR, et al. Interim clinical outcomes in the collaborative initial glaucoma treatment study comparing initial treatment randomized to medications or surgery. Ophthalmology. 2001;108:1943–1953. doi: 10.1016/S0161-6420(01)00873-9. [DOI] [PubMed] [Google Scholar]
- 12.Harizman N, et al. The ISNT rule and differentiation of normal from glaucomatous eyes. Archives of Ophthalmology. 2006;124:1579–1583. doi: 10.1001/archopht.124.11.1579. [DOI] [PubMed] [Google Scholar]
- 13.Jonas JB, Budde WM, Lang P. Neuroretinal rim width ratios in morphological glaucoma diagnosis. Br. J. Ophthalmol. 1998;82:1366–1371. doi: 10.1136/bjo.82.12.1366. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Schacknow, P. N. & Samples, J. R. The Glaucoma Book: A Practical Evidence-Based Approach to Patient Care, Springer, USA (2010).
- 15.Spaeth GL, Paulus A. The colored glaucoma graph and its use in caring for patients with glaucoma: A new system of management presented in three parts. Journal of Current Glaucoma Practice. 2010;4:83–90. doi: 10.5005/jp-journals-10008-1075. [DOI] [Google Scholar]
- 16.Henderer JD, et al. Reliability of the disc damage likelihood scale. Am. J. Ophthalmol. 2003;135:44–48. doi: 10.1016/S0002-9394(02)01833-0. [DOI] [PubMed] [Google Scholar]
- 17.Henderer JD. Disc damage likelihood scale. Br. J. Ophthalmol. 2006;90:395–396. doi: 10.1136/bjo.2005.083360. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Danesh-Meyer HV, Gaskin BJ, Jayusundera T, Donaldson M, Gamble GD. Comparison of disc damage likelihood scale, cup to disc ratio, and Heidelberg retina tomograph in the diagnosis of glaucoma. Br. J. Ophthalmol. 2006;90:437–441. doi: 10.1136/bjo.2005.077131. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Jonas JB, Papastathopoulos KI. Optic disc shape in glaucoma. Graefe’s Archive for Clinical and Experimental Ophthalmology. 1996;234:167–173. doi: 10.1007/BF02343067. [DOI] [PubMed] [Google Scholar]
- 20.Abdul Majid ASB, Kwag JH, Jim HB, Kim YD, Kang KD. Correlation between disc damage likelihood scale and optical coherence tomography in the diagnosis of glaucoma. Ophthalmologica. 2010;224:274–282. doi: 10.1159/000287350. [DOI] [PubMed] [Google Scholar]
- 21.Pahlitzsch M, et al. Significance of the disc damage likelihood scale objectively measured by a non-mydriatic fundus camera in preperimetric glaucoma. Clin. Ophthalmol. 2015;9:2147–2158. doi: 10.2147/OPTH.S93213. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Kara-José AC, et al. The disc damage likelihood scale: Diagnostic accuracy and correlations with cup-to-disc ratio, structural tests and standard automated perimetry. Plos One. 2017;12(7):e0181428–1–15. doi: 10.1371/journal.pone.0181428. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Danesh-Meyer HV, et al. Regional correlation of structure and function in glaucoma, using the disc damage likelihood scale, Heidelberg retina tomograph, and visual fields. Ophthalmology. 2006;113(4):603–611. doi: 10.1016/j.ophtha.2005.10.055. [DOI] [PubMed] [Google Scholar]
- 24.Hornová J, Navarro JBK, Prasad A, Freitas DG, Nunes CM. Correlation of disc damage likelihood scale, visual field, and Heidelberg retina tomograph II in patients with glaucoma. European Journal of Ophthalmology. 2018;18(5):739–747. doi: 10.1177/112067210801800513. [DOI] [PubMed] [Google Scholar]
- 25.Spaeth GL, Reddy SC. Imaging of the optic disc in caring for patients with glaucoma: Ophthalmoscopy and photography remain the gold standard. Surv. Ophthalmol. 2014;59(4):454–458. doi: 10.1016/j.survophthal.2013.10.004. [DOI] [PubMed] [Google Scholar]
- 26.Harish Kumar, J. R., Pediredla, A. K. & Seelamantula, C. S. Active discs for automated optic disc segmentation. Proc. IEEE Global Conference on Signal and Information Processing (GlobalSIP), 225–229 (2015).
- 27.Pediredla, A. K. & Seelamantula, C. S. A unified approach for optimization of snakuscules and ovuscules. Proc. 2012 IEEE International Conference on Acoustics, Speech and Signal Processing (ICASSP), 681–684 (2012).
- 28.Lalonde M, Beaulieu M, Gagnon L. Fast and robust optic disc detection using pyramidal decomposition and Hausdorff-based template matching. IEEE Transactions on Medical Imaging. 2001;20:1193–1200. doi: 10.1109/42.963823. [DOI] [PubMed] [Google Scholar]
- 29.Otsu N. A threshold selection method from gray-level histograms. IEEE Transactions on Systems, Man, and Cybernetics. 1979;9:62–66. doi: 10.1109/TSMC.1979.4310076. [DOI] [Google Scholar]
- 30.Liao P, Chen T, Chung P. A fast algorithm for multilevel thresholding. Journal of Information Science and Engineering. 2001;17:713–727. [Google Scholar]
- 31.Crum WR, Camara O, Hill DLG. Generalized overlap measures for evaluation and validation in medical image analysis. IEEE Transactions on Medical Imaging. 2006;25:1451–1461. doi: 10.1109/TMI.2006.880587. [DOI] [PubMed] [Google Scholar]
- 32.Chang HH, Zhuang AH, Valentino DJ, Chu WC. NeuroImage, Elsevier. 2009. Performance measure characterization for evaluating neuroimage segmentation algorithms; pp. 122–135. [DOI] [PubMed] [Google Scholar]
- 33.VISION: The Journal of the Missouri Optometric Association. New and revised ICD-9 codes for glaucoma, http://www.moavision.org/?p=590.
- 34.Decencire E, et al. Feedback on a publicly distributed database: the Messidor database. Image Analysis & Stereology. 2014;33:231–234. doi: 10.5566/ias.1155. [DOI] [Google Scholar]
- 35.Sivaswamy J, et al. A comprehensive retinal image dataset for the assessment of glaucoma from the optic nerve head analysis. JSM Biomedical Imaging. 2015;9:1–7. [Google Scholar]
- 36.Kauppi T, et al. Diaretdb1 diabetic retinopathy database and evaluation protocol. Technical Report. 2007;9:671–675. [Google Scholar]
- 37.Image Sciences Institute. DRIVE database, http://www.isi.uu.nl/Research/Databases/DRIVE/download.php.
- 38.Carmona EJ, Rincon M, Garcia-Feijoo J, Martinez-de-la-Casa JM. Identification of the optic nerve head with genetic algorithms. Artificial Intelligence in Medicine. 2008;43:243–259. doi: 10.1016/j.artmed.2008.04.005. [DOI] [PubMed] [Google Scholar]
- 39.Future of Ophthalmic Care. Forus Health, http://forushealth.com/.
- 40.Bosch Eye Care Solutions. Bosch Eye Care, http://www.bosch-eyecare.com/.
- 41.Image Processing and Analysis in Java. ImageJ, http://imagej.nih.gov/ij/index.html.
- 42.Schneider CA, Rasband WS, Eliceiri KW. NIH Image to ImageJ: 25 years of image analysis. Nature Methods. 2012;9:671–675. doi: 10.1038/nmeth.2089. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.