Methods for investigating the local spatial anisotropy and the preferred orientation of cones in adaptive optics retinal images

Vis Neurosci. 2016 Jan:33:E005. doi: 10.1017/S0952523816000018.

Abstract

The ability to noninvasively image the cone photoreceptor mosaic holds significant potential as a diagnostic for retinal disease. Central to the realization of this potential is the development of sensitive metrics for characterizing the organization of the mosaic. Here we evaluated previously-described and newly-developed (Fourier- and Radon-based) methods of measuring cone orientation in simulated and real images of the parafoveal cone mosaic. The proposed algorithms correlated well across both simulated and real mosaics, suggesting that each algorithm provides an accurate description of photoreceptor orientation. Despite high agreement between algorithms, each performed differently in response to image intensity variation and cone coordinate jitter. The integration property of the Fourier transform allowed the Fourier-based method to be resistant to cone coordinate jitter and perform the most robustly of all three algorithms. Conversely, when there is good image quality but unreliable cone identification, the Radon algorithm performed best. Finally, in cases where the cone coordinate reliability was excellent, the method previously described by Pum and colleagues performed best. These descriptors are complementary to conventional descriptive metrics of the cone mosaic, such as cell density and spacing, and have the potential to aid in the detection of photoreceptor pathology.

Keywords: Adaptive optics; Anisotropy; Cone metrics; Cone orientation; Cone photoreceptors.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Algorithms*
  • Anisotropy
  • Cell Count
  • Diagnostic Imaging / methods*
  • Diagnostic Techniques, Ophthalmological*
  • Female
  • Fourier Analysis
  • Humans
  • Male
  • Ophthalmoscopy / methods
  • Retinal Cone Photoreceptor Cells / cytology*