Foveal structure strongly correlates with its neurovascular organization. The findings support a developmental model in which the size of the FAZ determines the extent of centrifugal migration of inner retinal layers, which counteracts in some way the centripetal packing of cone photoreceptors.
Optical coherence tomography (OCT) allows high-resolution and noninvasive imaging of the structure of the retina in humans. This technique revolutionized the diagnosis of retinal diseases in routine clinical practice. Nevertheless, quantitative analysis of OCT scans is yet limited to retinal thickness measurements. We propose a novel automated method for the segmentation of eight retinal layers in these images. Our approach is based on global segmentation algorithms, such as active contours and Markov random fields. Moreover, a Kalman filter is designed in order to model the approximate parallelism between the photoreceptor segments and detect them. The performance of the algorithm was tested on a set of retinal images acquired in-vivo from healthy subjects. Results have been compared with manual segmentations performed by five different experts, and intra and interphysician variability has been evaluated as well. These comparisons have been carried out directly via the computation of the root mean squared error between the segmented interfaces, region-oriented analysis, and retrospectively on the thickness measures derived from the segmentations. This study was performed on a large database including more than seven hundred images acquired from more than one hundred healthy subjects. OCT image enhancement, by performing image equalization [9], applying directional filters [9] or coherence-enhanced diffusion filtering [10]; A-scans (columns) alignment with regard to a reference retina layer, determined by cross correlation of adjacent columns [6] or with regard to an already detected interface [9,11]. The filtered OCT images are then passed to the interface detection process. This second step is generally based on the search for peak Contents lists available at ScienceDirect
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