Scale Adjustments to Facilitate Two-Dimensional Measurements in OCT Images

PLoS One. 2015 Jun 25;10(6):e0131154. doi: 10.1371/journal.pone.0131154. eCollection 2015.

Abstract

Purpose: To address the problem of unequal scales for the measurement of two-dimensional structures in OCT images, and demonstrate the use of intra¬ocular objects of known dimensions in the murine eye for the equal calibration of axes.

Methods: The first part of this work describes the mathematical foundation of major distortion effects introduced by X-Y scaling differences. Illustrations were generated with CorelGraph X3 software. The second part bases on image data obtained with a HRA2 Spectralis (Heidelberg Engineering) in SV129 wild-type mice. Subretinally and intravitreally implanted microbeads, alginate capsules with a diameter of 154±5 μm containing GFP-marked mesenchymal stem cells (CellBeads), were used as intraocular objects for calibration.

Results: The problems encountered with two-dimensional measurements in cases of unequal scales are demonstrated and an estimation of the resulting errors is provided. Commonly, the Y axis is reliably calibrated using outside standards like histology or manufacturer data. We show here that intraocular objects like dimensionally stable spherical alginate capsules allow for a two-dimensional calibration of the acquired OCT raw images by establishing a relation between X and Y axis data. For our setup, a correction factor of about 3.3 was determined using both epiretinally and subretinally positioned beads (3.350 ± 0.104 and 3.324 ± 0.083, respectively).

Conclusions: In this work, we highlight the distortion-related problems in OCT image analysis induced by unequal X and Y scales. As an exemplary case, we provide data for a two-dimensional in vivo OCT image calibration in mice using intraocular alginate capsules. Our results demonstrate the need for a proper two-dimensional calibration of OCT data, and we believe that equal scaling will certainly improve the efficiency of OCT image analysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Eye / anatomy & histology
  • Green Fluorescent Proteins
  • Image Processing, Computer-Assisted / statistics & numerical data
  • Mice
  • Mice, 129 Strain
  • Ophthalmoscopy / statistics & numerical data
  • Retina / anatomy & histology
  • Retinal Vessels / anatomy & histology
  • Tomography, Optical Coherence / statistics & numerical data*

Substances

  • Green Fluorescent Proteins

Grants and funding

This work was supported by the German Ministry of Education and Research (BMBF, HOPE2 01GM1108A) and by the Deutsche Forschungsgemein schaft and Open Access Publishing Fund of University of Tuebingen. Dr. Susanne C Beck received a grant from Heidelberg Engineering GmbH. The funders provided support in the form of salaries for authors [SCB], but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. This specific roles of these authors are articulated in the ‘author contribution’ section.