Slope Chain Code-based scale-independent tortuosity measurement on retinal vessels

IF 3 2区 医学 Q1 OPHTHALMOLOGY
Zian Fanti , Ulf-Dietrich Braumann , Franziska G. Rauscher , Thomas Ebert , Ernesto Bribiesca , M. Elena Martinez-Perez
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引用次数: 0

Abstract

Retinal vascular tortuosity presents valuable potential as a clinical biomarker for many relevant vascular and systemic diseases. Our work exhibits twofold: first, the definition of a novel scale-invariant metric to measure retinal blood vessel tortuosity; and second, the generation of a local database, called SCALE-TORT, with the intention of providing a means to test the scale invariance property on real retinal vessels rather than on synthetic data. The proposed scale invariant tortuosity metric is based on the Extended Slope Chain Code which uses variable straight-line segments for describing curves. It is focused on the representation of high-definition curves, the length of the segments is a function of the slope changes of the curve. Scale invariance is an important property when several different retinal image settings or different acquisition sources are used during a particular study or in clinical practice. The database SCALE-TORT, introduced herein, was built semi-automatically from digital images containing the coordinates of blood vessel central lines (curves) taken from images of the same eye obtained by two different imaging methodologies: retinal fundus camera and scanning laser ophthalmoscope. The vessel curves extracted from the same eye are paired for images acquired by the fundus camera and those acquired by the scanning laser ophthalmoscope to evaluate the scale invariance of the metric. Ten different tortuosity metrics were implemented and compared including our proposed metric. Three experiments were conducted to test the metrics and their properties. The first aimed to determine which tortuosity metrics possess the following properties: scale invariance, sensitivity to sudden tortuosity changes when the curve remains constant in size, and how they behave when curves are concatenated. In the second experiment, all reviewed metrics were tested on the publicly available RET-TORT database, to compare the results of the specific metric with the tortuosity classification provided by their experts and in comparison with other authors. Finally, in the third experiment, the behavior of different metrics, including those which are scale-invariant, were tested by utilizing the paired retinal vessel curves from our new SCALE-TORT database. In comparison with other tortuosity metrics, we show that the metric Extended Slope Chain Code proposed in this work optimally complies with scale invariance, in addition to having sufficient sensitivity to detect abrupt changes in tortuosity. Easy implementation being a further plus. Furthermore, we present a new and valuable database for scale property evaluation on images of retinal blood vessels called SCALE-TORT. As far as we are aware, there is no public database with these characteristics.

Abstract Image

基于斜率链码的视网膜血管尺度无关扭曲度测量。
视网膜血管扭曲作为许多相关血管和全身性疾病的临床生物标志物具有宝贵的潜力。我们的工作展示了两个方面:首先,定义了一种新的尺度不变度量来测量视网膜血管弯曲度;第二,生成一个称为scale - tort的本地数据库,旨在提供一种方法来测试真实视网膜血管的尺度不变性,而不是在合成数据上。提出了一种基于扩展斜率链码的尺度不变曲率度量方法,该方法使用可变直线段来描述曲线。它侧重于高清晰曲线的表示,线段的长度是曲线斜率变化的函数。在一个特定的研究或临床实践中,当使用几种不同的视网膜图像设置或不同的采集源时,尺度不变性是一个重要的特性。本文介绍的SCALE-TORT数据库是由两种不同成像方法(视网膜眼底相机和扫描激光检眼镜)获得的同一只眼睛的图像中含有血管中心线(曲线)坐标的数字图像半自动构建而成的。将同一只眼睛提取的血管曲线与眼底相机采集的图像和扫描激光检眼镜采集的图像进行配对,评价度量的尺度不变性。实现并比较了10种不同的扭曲度度量,包括我们提出的度量。进行了三个实验来测试度量及其特性。第一个目标是确定哪些扭曲度指标具有以下属性:尺度不变性,当曲线保持恒定大小时对突然扭曲度变化的敏感性,以及当曲线连接时它们的行为。在第二个实验中,所有评审的指标都在公开的RET-TORT数据库上进行了测试,将特定指标的结果与专家提供的扭曲度分类结果进行了比较,并与其他作者进行了比较。最后,在第三个实验中,利用我们新的SCALE-TORT数据库中的成对视网膜血管曲线,测试了不同指标的行为,包括那些尺度不变的指标。与其他扭曲度度量相比,我们证明了本文提出的度量扩展斜率链码最优地符合尺度不变性,并且具有足够的灵敏度来检测扭曲度的突变。易于实现是进一步的优势。此外,我们还提出了一种新的、有价值的视网膜血管图像尺度特性评估数据库scale - tort。据我们所知,目前还没有具备这些特征的公共数据库。
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来源期刊
Experimental eye research
Experimental eye research 医学-眼科学
CiteScore
6.80
自引率
5.90%
发文量
323
审稿时长
66 days
期刊介绍: The primary goal of Experimental Eye Research is to publish original research papers on all aspects of experimental biology of the eye and ocular tissues that seek to define the mechanisms of normal function and/or disease. Studies of ocular tissues that encompass the disciplines of cell biology, developmental biology, genetics, molecular biology, physiology, biochemistry, biophysics, immunology or microbiology are most welcomed. Manuscripts that are purely clinical or in a surgical area of ophthalmology are not appropriate for submission to Experimental Eye Research and if received will be returned without review.
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