Intra-retinal layer segmentation of 3D optical coherence tomography using coarse grained diffusion map

被引:127
|
作者
Kafieh, Raheleh [1 ]
Rabbani, Hossein [1 ,2 ]
Abramoff, Michael D. [2 ]
Sonka, Milan [2 ]
机构
[1] Isfahan Univ Med Sci, Phys & Biomed Engn Dept, Med Image & Signal Proc Res Ctr, Esfahan, Iran
[2] Univ Iowa, Iowa Inst Biomed Imaging, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
Optical coherence tomography (OCT); Segmentation; Spectral graph theory; Diffusion map; AUTOMATIC SEGMENTATION; THICKNESS PROFILES; OCT; GEOMETRY;
D O I
10.1016/j.media.2013.05.006
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Optical coherence tomography (OCT) is a powerful and noninvasive method for retinal imaging. In this paper, we introduce a fast segmentation method based on a new variant of spectral graph theory named diffusion maps. The research is performed on spectral domain (SD) OCT images depicting macular and optic nerve head appearance. The presented approach does not require edge-based image information in localizing most of boundaries and relies on regional image texture. Consequently, the proposed method demonstrates robustness in situations of low image contrast or poor layer-to-layer image gradients. Diffusion mapping applied to 2D and 3D OCT datasets is composed of two steps, one for partitioning the data into important and less important sections, and another one for localization of internal layers. In the first step, the pixels/voxels are grouped in rectangular/cubic sets to form a graph node. The weights of the graph are calculated based on geometric distances between pixels/voxels and differences of their mean intensity. The first diffusion map clusters the data into three parts, the second of which is the area of interest. The other two sections are eliminated from the remaining calculations. In the second step, the remaining area is subjected to another diffusion map assessment and the internal layers are localized based on their textural similarities. The proposed method was tested on 23 datasets from two patient groups (glaucoma and normals). The mean unsigned border positioning errors (mean +/- SD) was 8.52 +/- 3.13 and 7.56 +/- 2.95 mu m for the 2D and 3D methods, respectively. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:907 / 928
页数:22
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