Abstract

Keratocytes are fibroblast-like cells that maintain the optical clarity and the overall health of the cornea. The ability to measure precisely their density and spatial distribution in the cornea is important for the understanding of corneal healing processes and the diagnostics of some corneal disorders. A novel computerized approach to detection and counting of keratocyte cells from ultra high resolution optical coherence tomography (UHR-OCT) images of the human corneal stroma is presented. The corneal OCT data is first processed using a state-of-the-art despeckling algorithm to reduce the effect of speckle on detection accuracy. A thresholding strategy is then employed to allow for improved delineation of keratocyte cells by suppressing similarly shaped features in the data, followed by a second-order moment analysis to identify potential cell nuclei candidates. Finally, a local extrema strategy is used to refine the candidates to determine the locations and the number of keratocyte cells. Cell density distribution analysis was carried in 3D UHR-OCT images of the human corneal stroma, acquired in-vivo. The cell density results obtained using the proposed novel approach correlate well with previous work on computerized keratocyte cell counting from confocal microscopy images of human cornea.

Highlights

  • Keratocytes are specialized fibroblasts, located in-between the collagen fibers comprising the matrix of the human corneal stroma [1, 2, 3]

  • To evaluate the effectiveness of the computerized keratocyte cell detection and counting approach, it was applied to multiple 3D sets of human corneal images acquired in-vivo with a research grade high speed, UHR-Optical coherence tomography (OCT) system operating in the 1060nm wavelength region

  • Keratocyte cell density analysis was carried out in a region of the stroma corresponding to a 1mm × 1mm surface area, centered around the apex of the volumetric OCT image of the cornea

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Summary

Introduction

Keratocytes are specialized fibroblasts, located in-between the collagen fibers comprising the matrix of the human corneal stroma [1, 2, 3]. If our hypothesis is correct, the number of highly reflective spots per unit volume of tissue, identified from a 3D image set of UHR-OCT tomograms of human corneal stroma should correlate well with the cell number density measured from a 3D set of confocal images of the stroma. Based on this hypothesis, we have developed an automatic algorithm for identification and counting of keratocytes from UHR-OCT corneal tomograms

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