Development of an automated system to classify retinal vessels into arteries and veins

https://doi.org/10.1016/j.cmpb.2012.02.008Get rights and content

Abstract

There are some evidence of the association between the calibre of the retinal blood vessels and hypertension. Computer-assisted procedures have been proposed to measure the calibre of retinal blood vessels from high-resolution photopraphs. Most of them are in fact semi-automatic. Our objective in this paper is twofold, to develop a totally automated system to classify retinal vessels into arteries and veins and to compare the measurements of the arteriolar-to-venular diameter ratio (AVR) computed from the system with those computed from observers.

Our classification method consists of four steps. First, we obtain the vascular tree structure using a segmentation algorithm. Then, we extract the profiles. After that, we select the best feature vectors to distinguish between veins and arteries. Finally, we use a clustering algorithm to classify each detected vessel as an artery or a vein.

Our results show that compared with an observer-based method, our method achieves high sensitivity and specificity in the automated detection of retinal arteries and veins. In addition the system is robust enough independently of the radii finally chosen, which makes it more trustworthy in its clinical application. We conclude that the system represents an automatic method of detecting arteries and veins to measure the calibre of retinal microcirculation across digital pictures of the eye fundus.

Introduction

The retina is the only place where the vascular system is visible using simple instrumentation. There are several studies providing some evidence of the association between the calibre of the retinal blood vessels, i.e. arteries and veins, and diabetes [1], as well as cardiovascular diseases such as hypertension, strokes, and coronary heart disease [2], [3], [4], [5], [6], [7]. Narrower retinal arteriolar calibre has been associated with hypertension and may even precede clinical hypertension [3], [4], [5], [8], [9]. In contrast, wider venular calibre has been shown to be associated with an increased risk of stroke and cardiovascular events [7], [10], [11], [12]. A measurement that has been used to quantify these variations in the calibre of the vessels is the arteriolar-to-venular diameter ratio (AVR) [3].

To achieve accurate and, more importantly, reproducible results, computer-assisted procedures have been proposed to measure the calibre of retinal blood vessels from high-resolution photopraphs [3], [13], [14], [15], [16], [17], [18], [19], [20], [21], [22], [23], [24], [25], [26], [27]. Most of these procedures are in fact semi-automatic [14], [15], [16], [17], [18], [20], [21], [25], [26], in the sense that they involve a manual function where a skilled observer must first determine the vessel type, artery or vein. In fact, our group recently described a semi-automatic computerised system for evaluation of the AVR that has shown very good reproducibility [28]. Using this method we observed a regression of early hypertension-related alterations in retinal microcirculation after 6 months of antihypertensive treatment [17].

In light of this, we have tried to improve the specificity of the linear method we used by applying a model based on elastic curves called ‘snakes’ [29], with which the specificity is improved, supporting the same sensitivity in the detection of retinal vessels, but which continues to have the limitations of a semi-automatic method that needs the intervention of an observer, thus limiting its application to clinical practice.

An automatic method was already proposed in 2003 by Grisan and Ruggeri [13]. Two were the main differences with respect to the method we proposed here. First, in Grisan and Ruggeri's method, images were first pre-processed in order to compensate both, intra and inter-variability. Second, analyses were restricted to main vessels, excluding small arterioles and venoules [13]. In fact, whereas for main vessels (i.e. those belonging to the main vascular arcades) results were very good (only 6.7% of error), results corresponding to secondary vessels were not so satisfactory (20.7% of error).

Recently, Niemeijer et al. [27] also propose an automatic procedure in classifying retinal vessels into arteries and veins. The procedure provides very good results (area under the ROC of 0.88). However, it is applied only to large vessels, because they tend to be easier to classify and they do not require the use of vessel connectivity Information [27].

Our main objective in this paper is to develop a totally automated system to classify all the retinal vessels (large and smaller) into arteries and veins. However, as stated above, our final aim is to develop a system that can be easily applied to clinical practice. Therefore, our secondary objective is to compare the measurements of the AVR computed with the results obtained from the system with those computed with the results from observers. In fact, very recently, Tramontan et al. [30] proposed a web tool for the AVR estimation, very similar to that described here.

This paper is organised as follows. After the short introduction given in this section, we describe in detail our classification methodology in Section 2. In Section 3 we provide the material and the materials in order to validate our proposed system. In Section 4, we provide the results of the validation and also use these results to measure the AVR. Finally, we finish with Section 5, where we provide some concluding remarks and Section 6 where we give our conclusions.

Section snippets

Theory

Our classification method consists of four steps, as Fig. 1 shows. First, we obtain the vascular tree structure for all, large and smaller vessels, using a segmentation algorithm that has been validated in daily medical practice. Then, we extract the profiles, that is, the vessel point sets where the feature vectors are obtained. After that, we select the best feature vectors to distinguish between veins and arteries. Finally, we use a clustering algorithm to classify each detected vessel as an

Material and methods

An interactive web application for the management of retinal image screening processes (SIRIUS) has been developed [38], [39]. The system is currently being used by several hospitals to analyse the results of the pharmacologic treatment of hypertensive patients.

Fifty-eight colour retinal images, taken from 58 different subjects, were used to validate our proposed system. These images were obtained from recently diagnosed hypertensive subjects, participating in both the SIRIUS-Postel [28] and

Validity results

Whereas the system did not label 1.3% of all vessels (that is the type of the vessel), 28.4% of the vessels were not classified by the observers (22.9% the observer 1, 35.2% the observer 2, and 27.2% the observer 3). The failure by the observer to identify the vessel type did not depend on the radius where the mark was located, i.e. 19.6% were not labelled in the radius 1, 21.4% in radius 2, 21.3% in radius 3, 19.6% in radius 4, and 18.1% in radius 5. The failure to identify obviously depended

Discussion

Some years ago we described and validated a semiautomatic method for the determination of vascular retinal calibre and the arteriolar-to-venular diameter ratio, and its usefulness in the diagnosis and evaluation of antihypertensive treatment [17]. This method, which was linear and called ART-VEIN, was based on mathematical models. It achieved high sensitivity in the detection of retinal micro-vessels but was lacking in specificity, for many of the images detected as vessels by the linear method

Conclusions

We conclude that the system represents an automatic method of detecting arteries and veins to measure the calibre of retinal microcirculation across digital pictures of the eye fundus. It estimates arteriolar-to-venular diameter, determined from the relationship between the average arteriolar and venular calibre, with high sensitivity and specificity, which means it can be used in clinical research and it avoids bias introduced by an observer.

Conflicts of interest statement

There are no conflicts of interest for any of the authors. All authors disclose any financial and personal relationships with other people or organisations that could inappropriately influence and/or bias their work.

Acknowledgements

This work was partly funded under projects ETES-FIS 08/90420, ETES-FIS 08/90539 and ETES-FIS 08/90549 of the ‘Fondo de Investigación Sanitaria’ (Health Research Fund, FIS), Ministry of Science and Innovation, Spain, project AATRM 155/12/2004 of the ‘Agència d’Avaluació de Tecnologia i Recerca Mèdiques’ (Catalan Agency for Health Technology Assessment and Research, CAHTA), the ‘Servei Català de la Salut’ (Catalan Health Service), ‘Generalitat de Catalunya’ (Government of Catalonia), and under

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